Detailed Program
UTC/GMT +1 hour
09:15 - 09:30
Accreditation
08:30 - 19:30
09:15 - 09:30
Opening Cerimony
09:30 - 10:30
EDP Labelec Main Stage
09:15 - 09:30
A Felicidade é Lucrativa
10:30 - 11:15
EDP Labelec Main Stage

Ricardo Costa is an entrepreneur, international speaker, and author of the book “A Felicidade é Lucrativa”. He is the President of the Bernardo da Costa Group, holds leadership roles in several companies, and serves as a Board Advisor across different sectors. With an International MBA from Católica Porto Business School and a degree in Industrial Engineering and Management, he is also a visiting professor at business schools and one of the leading advocates of the importance of happiness in the workplace.
Beyond his business activities, he is a columnist for the newspapers Expresso and Record, Honorary Consul of Kosovo, and President of the General Council of AEMinho. His experience and strategic vision make him a reference in the fields of leadership, innovation, and corporate happiness.
Abstract
Temas a abordar: Transições em curso no Mundo; Criação do Departamento da Felicidade; Estratégias para conseguirmos ambientes saudáveis e produtivos; Monitorização de KPI’s; Pilares de uma Liderança Humanizada
09:15 - 09:30
Break Time
11:15 - 11:30
09:15 - 09:30
Compliance em Solos Resíduos e Perigosídade: da Amostra ao Resultado
11:30 - 12:10
Eurofins Stage
Speaker
Alda Enriques, EUROFINS
Abstract
Available Soon
Superpower Skills for Modern Labs
09:15 - 09:30
11:30 - 12:10
Ambidata Stage
Speaker
Margarida Ségard, ISQ
09:15 - 09:30
The Lab of the Future project
11:30 - 12:10
Normax Stage

Laura Martin has been the EUROLAB Secretary General since 2022. Prior to this position, she has undergone various responsibilities, taking the first role in EUROLAB back in 2013. Before, she worked for DG CONNECT at the European Commission, as well as for other international organisations based in Brussels, taking on various roles such as Communications Manager and International Affairs Manager. She holds extensive experience in EU-funded projects, as well as stakeholders’ engagement, having worked in her roles with both public and private sectors representative for the laboratory community. She holds a diploma in Journalism, a master’s degree in Communications Studies, and a bachelor’s in Modern Languages and Translation.
Paulo Rego
Abstract
The Lab of the Future project will significantly enhance the understanding of how digitalisation and sustainability are reshaping laboratory environments across Europe. It will make it easier for education providers, laboratories and organisations to identify opportunities for collaboration and innovation within this evolving ecosystem.
09:15 - 09:30
Portugal Clinical Studies Platform: A Single Point of Contact for Clinical Research
11:30 - 12:10
Inês de Castro
Speaker
Inês Moreira, AICIB
Abstract
Available Soon
09:15 - 09:30
ISO 17034: Uso de Materiales de Referencia Certificados como Patrón
11:30 - 12:10
Sondar Stage

ISO-17034: The use of certified reference materials as standards
The UNE-EN ISO 17034 standard defines the requirements for producing certified reference materials (CRMs), which are essential for traceability and quality in critical environments, including homogeneity and stability, thereby enabling their use as a reliable reference over time. This contributes to regulatory compliance in sectors such as inspection and control bodies, the automotive industry and certified laboratories.
The presentation will demonstrate how reference materials act as standards for calibration, reducing uncertainty and ensuring metrological traceability of results. Benefits for laboratories, manufacturers and regulatory bodies will be discussed, including proposals for integrating CRMs into metrological management systems. This contribution promotes technical excellence and metrological innovation in Portugal.
Abstract
La norma UNE-EN ISO 17034 define los requisitos para producir materiales de referencia certificados (MRC), esenciales para trazabilidad y calidad en entornos críticos incluyendo la homogeneidad y la estabilidad, permitiendo su uso como referencia confiable a lo largo del tiempo. Contribuyendo a la conformidad normativa en sectores como inspección y organismos de control, automoción y laboratorios certificados. La ponencia mostrará cómo los materiales de referencia actúan como patrones para calibración, reduciendo incertidumbre y asegurando trazabilidad metrológica de los resultados. Se abordarán beneficios para laboratorios, fabricantes y organismos reguladores, incluyendo casos prácticos y propuestas para integrar los MRC en sistemas de gestión metrológica. Esta contribución impulsa la excelencia técnica y la innovación metrológica en Portugal.
09:15 - 09:30
From Concept to Creation: A Hands-on Additive Manufacturing Workshop
11:30 - 12:10
Envienergy Stage

A Materials Engineer and R&D specialist with a focus on advanced manufacturing technologies, particularly additive manufacturing and robotic-based fabrication at ISQ. His work centers on bridging materials science and engineering practice, developing solutions that integrate material selection, process optimization, and digital design to enable the production of functional components. He has experience in engineering design, 3D modelling, and prototyping through additive manufacturing, supporting the development and validation of industrial systems and equipment. Through his professional and research activities, he has contributed to the development of experimental setups, materials characterization methodologies, and engineering prototypes.

Francisco Feliciano completed his master’s degree in Engineering Physics at the Faculty of Sciences of the University of Lisbon (FCUL) in 2023. He currently works as a Researcher at the Institute of Welding and Quality (ISQ) focusing on metal additive manufacturing technologies, particularly Directed Energy Deposition (DED) processes. His work also includes Design for Additive Manufacturing (DfAM) and the simulation of additive manufacturing processes, supporting the optimization and efficiency of additive fabrication. Through the projects developed at ISQ, he has also gained experience in the characterization of materials used in additive manufacturing.

Paulo J. Morais holds a PhD and a degree in Materials Engineering from the University of Lisbon (Instituto Superior Técnico). Since 2001, he has been a Senior Researcher and Project Manager at Instituto de Soldadura e Qualidade (ISQ), where he currently leads the Additive Manufacturing Laboratory. His expertise lies in R&D for production technologies and advanced materials processing, with a broad focus on driving industrial innovation. He has coordinated numerous national and international R&D projects and contributed to conferences, journals, and books. He also plays an active role in international qualification standards, chairing the examination panel for the ISQ Additive Manufacturing Authorised Nominated Body (AM-ANB) within the European Welding Federation system and representing ISQ in the International Additive Manufacturing Qualification Council (IAMQC).

Rodolfo Batalha is PhD materials scientist specializing in physical metallurgy, welding, rapid solidification, and metal additive manufacturing. With a strong foundation in physical metallurgy and industrial experience in the steel sector, he leads research initiatives in titanium-based biocompatible alloys and next-generation alloy systems engineered for additive manufacturing. As a researcher at Instituto de Soldadura e Qualidade, he drives innovation in Powder Bed Fusion-Laser Beam (PBF-LB), focusing on process optimization, microstructure engineering, and performance enhancement of metallic components. His work integrates fundamental metallurgical principles with applied engineering strategies, supporting the advancement of next-generation metallic materials and additive manufacturing technologies.
Abstract
Move beyond theory and dive into the practical workflow of additive manufacturing (AM) in this hands-on workshop. Participants will be presented with a real-world industrial challenge requiring the production of a component via 3D printing. To solve this problem, attendees will form three specialized, collaborative teams: one focused on material and process selection (evaluating suitable materials based on performance requirements and proper AM process), one on 3D design and simulation (modelling the component for function and manufacturability), and one on 3D printing (slicing, setting up, and running the print). By working together, participants will gain practical insight into the multidisciplinary decisions involved in turning an engineering concept into a manufactured part.
09:15 - 09:30
Characterization of Nitrogen Oxide Emissions in Domestic Gas Appliances
11:30 - 12:10
Cytosens Stage

Abstract
NOx emissions in domestic gas appliances represent a critical challenge in terms of environmental impact, measurement accuracy, and regulatory compliance. Leveraging its expertise, CATIM supports industry in meeting regulatory requirements, actively participates in the development of standardized methodologies for the measurement of nitrogen oxides, and addresses the associated technical challenges, thereby contributing to more sustainable gas technologies.
09:15 - 09:30
Break Time
12:10 - 12:20
09:15 - 09:30
The Next Operational Layer: AI Agents in Practice in Laboratories
12:20 - 13:00
Eurofins Stage

With over 25 years of experience in the field of information systems, he currently holds the role of Head of Ai and Project Manager at Ambidata Lda and is a professor in Computer Engineering at ISEP. He has worked in virtually every area of software engineering, from programmer to CTO. He has various skills in software development and LIMS products, including: analysis, databases, project management, requirements engineering, and innovation. He is now dedicated to exploring how AI can revolutionize data-driven processes.
Abstract
Artificial Intelligence is evolving toward increasingly agent-oriented models, often referred to as Agentic AI. In many laboratories, this evolution is already becoming operational. This session explores what it means to deploy AI agents within a production LIMS environment, how they operate continuously, what signals they generate, and how those signals reach both technical teams and management in a structured way. Real examples from a production system will be presented. By introducing AI agents as a structured operational layer, laboratories can anticipate critical situations earlier, take decisions with greater confidence, and preserve traceability and technical responsibility.
09:15 - 09:30
O Preço Invisível De Liderar
12:20 - 13:00
Ambidata Stage

Professional with 14 years of experience in developing leaders in both sports and corporate contexts. Specialist in leadership, communication, and emotional intelligence applied to individual and team performance. Certified in Coaching since 2012, with solid practice in mentoring and group facilitation.
Experienced in supporting managers, coaches, and professionals in goal setting and overcoming challenges. Skilled in team management, motivation, assertive communication, and leadership development. Focused on sustainable results by combining organizational performance with human growth.
Abstract
Liderar não é apenas definir estratégias, gerir equipas ou alcançar resultados. Existe um preço invisível que muitos líderes pagam em silêncio: a solidão do papel, o peso das decisões difíceis e a culpa associada à responsabilidade de impactar pessoas e organizações. Nesta palestra, Flávia Gouveia explora a dimensão emocional da liderança e o impacto que emoções não geridas têm na tomada de decisão, na comunicação e no clima das equipas. A sessão convida os participantes a refletir sobre os desafios internos que acompanham o exercício da liderança e sobre a importância da autoliderança como base para uma liderança mais consciente, humana e sustentável. Com uma abordagem prática e orientada para a realidade das organizações, serão partilhadas reflexões e ferramentas que ajudam os líderes a reconhecer este desgaste invisível, a gerir melhor a pressão e a fortalecer a sua capacidade de liderar com clareza, equilíbrio emocional e impacto positivo.
09:15 - 09:30
Micropipettes: Good practices for Use, Maintenance, and Calibration
12:20 - 13:00
Normax Stage
Speaker
Isabel Faria, Normax
Abstract
Every instrument drifts. How to choose a micropipette for each application, how to avoid pipetting errors, how to implement a maintenance and calibration plan, how to establish acceptance criteria, and how to apply them simply.
09:15 - 09:30
Upscalling and Process Control in Health Products: from Lab to Industrial Production
12:20 - 13:00
Inês de Castro

Rita Palmeira de Oliveira holds a PhD in Pharmaceutical Sciences (field of Pharmaceutical Technology) and two professional specializations in Hospital Pharmacy and Pharmaceutical Industry (Qualified Person title). She is an invited professor at University of Beira Interior (Covilhã, Portugal), where she teaches Pharmaceutical Technology and Cosmetic Sciences. She is a member of RISE HEALTH-UBI. Rita is the co-Founder and Technical Director of Labfit and Pharmapoli (two brands of Health Products Research and Development Lda) that provide laboratory services and contract manufacturing/private label services, respectively, for cosmetics and medical devices.
Abstract
This lecture explores how cosmetic and medical device formulations can be designed from the first step to ensure smooth, efficient, and compliant industrial-scale manufacturing. The session highlights the critical differences between lab-scale development and full-scale production, emphasizing the importance of process robustness, raw-material standardization, regulatory expectations, and cross-functional communication. Attendees will gain practical insight into crytical steps in formulation and process design with scalability in mind, reducing time-to-market, minimizing manufacturing deviations, and improving product quality and operational reliability. The presentation provides actionable frameworks, real-world examples, and practical strategies to help laboratory professionals anticipate scale-up challenges, control critical quality attributes (CQAs), and ensure seamless technology transfer into production environments aligned with Good Manufacturing Practices (GMP) described in ISO 22716 and ISO 13485.
09:15 - 09:30
When Every Drop Makes a Difference: Innovation in Volume and Flow Measurement in Healthcare
12:20 - 13:00
Sondar Stage

Dr. Elsa Batista holds a PhD in Mechanical Engineering from Universidade Nova de Lisboa / Faculty of Sciences and Technology (FCT/UNL). She has been responsible for the Volume and Flow Laboratory of the Portuguese Institute for Quality (IPQ) since 2002, having joined the institute in 1999. Dr. Batista serves as the convenor of the Volume Subgroup of EURAMET Technical Committee for Flow and is the Portuguese representative to this committee. She is an active member of several international standardization committees, including ISO/TC 48, ISO/TC 28, ISO/TC 276, and ISO/TC 84, and currently chairs ISO/TC 48/SC 8. She is also a board member of both the Microfluidics Association and the SPMET Association. In 2023, she received the CEN–CENELEC Standards + Innovation Award in the Individual Researcher category. She is presently the coordinator of the EURAMET international project “MFMET – Establishing Metrology Standards in Microfluidic Devices II.
Abstract
The measurement of liquid flow, both inside and outside the human body, plays a crucial role in medical technology. The safety and reliability of numerous medical devices - such as dialysis machines, infusion devices, and liquid handling systems for in vitro diagnostics that work at ultra low flow rates - depend on the precise and safe dosing of fluids.
For critical infusion applications involving vulnerable patients, it is essential to ensure rigorous and well controlled drug administration. This can only be achieved through improved dosing accuracy and traceable measurement of all relevant quantities, namely volume, flow rate, and pressure, both in drug delivery devices and in inline sensors operating at very low flow rates. In parallel, the development of advanced diagnostic technologies such as organ on chip systems has further reinforced the need for highly precise flow measurements. These biomimetic microdevices - which simulate the function of human organs through perfused microchannels - rely on extremely well controlled flows to deliver reliable results in pharmacological testing, toxicology studies, and diagnostic applications. Accurate perfusion of nutrients, drugs, or biomarkers within organ on chip platforms is essential for reproducibility and for the metrological validation of the biological responses observed. High precision flow and pressure sensors are therefore critical to ensuring the performance and traceability of these innovative systems. In this context, the contribution of the metrological infrastructures recently implemented in European National Metrology Institutes, within the scope of the European projects: MeDD - Metrology for Drug Delivery and MFMET - Establishing Metrology Standards in Microfluidic Devices, has been fundamental not only for ensuring safer infusion therapy in healthcare, but also for supporting the development and validation of new diagnostic platforms, including technologies based on organ on chip systems. In these areas, accuracy, traceability, and comparability of measurements are decisive factors for patient safety and for confidence in laboratory results. At IPQ’s Volume and Flow Laboratory, several advanced gravimetric and optical flow measurement techniques have been developed and validated. These innovations have enabled the expansion of IPQ’s calibration capabilities and the formal publication of new Measurement Calibration Capabilities (CMCs). As a result, the laboratory can now calibrate high precision flow measurement instruments operating across a wide range - from 0,0003 mL/h to 2000 mL/h - covering ultra low microfluidic regimes up to clinically and industrially relevant flow rates. This enhanced capability supports applications in medical devices, pharmaceutical technologies, microfluidics, and emerging fields such as organ on chip and diagnostic microsystems.
09:15 - 09:30
From Concept to Creation: A Hands-on Additive Manufacturing Workshop
12:20 - 13:00
Envienergy Stage

A Materials Engineer and R&D specialist with a focus on advanced manufacturing technologies, particularly additive manufacturing and robotic-based fabrication at ISQ. His work centers on bridging materials science and engineering practice, developing solutions that integrate material selection, process optimization, and digital design to enable the production of functional components. He has experience in engineering design, 3D modelling, and prototyping through additive manufacturing, supporting the development and validation of industrial systems and equipment. Through his professional and research activities, he has contributed to the development of experimental setups, materials characterization methodologies, and engineering prototypes.

Francisco Feliciano completed his master’s degree in Engineering Physics at the Faculty of Sciences of the University of Lisbon (FCUL) in 2023. He currently works as a Researcher at the Institute of Welding and Quality (ISQ) focusing on metal additive manufacturing technologies, particularly Directed Energy Deposition (DED) processes. His work also includes Design for Additive Manufacturing (DfAM) and the simulation of additive manufacturing processes, supporting the optimization and efficiency of additive fabrication. Through the projects developed at ISQ, he has also gained experience in the characterization of materials used in additive manufacturing.

Paulo J. Morais holds a PhD and a degree in Materials Engineering from the University of Lisbon (Instituto Superior Técnico). Since 2001, he has been a Senior Researcher and Project Manager at Instituto de Soldadura e Qualidade (ISQ), where he currently leads the Additive Manufacturing Laboratory. His expertise lies in R&D for production technologies and advanced materials processing, with a broad focus on driving industrial innovation. He has coordinated numerous national and international R&D projects and contributed to conferences, journals, and books. He also plays an active role in international qualification standards, chairing the examination panel for the ISQ Additive Manufacturing Authorised Nominated Body (AM-ANB) within the European Welding Federation system and representing ISQ in the International Additive Manufacturing Qualification Council (IAMQC).

Rodolfo Batalha is PhD materials scientist specializing in physical metallurgy, welding, rapid solidification, and metal additive manufacturing. With a strong foundation in physical metallurgy and industrial experience in the steel sector, he leads research initiatives in titanium-based biocompatible alloys and next-generation alloy systems engineered for additive manufacturing. As a researcher at Instituto de Soldadura e Qualidade, he drives innovation in Powder Bed Fusion-Laser Beam (PBF-LB), focusing on process optimization, microstructure engineering, and performance enhancement of metallic components. His work integrates fundamental metallurgical principles with applied engineering strategies, supporting the advancement of next-generation metallic materials and additive manufacturing technologies.
Abstract
Move beyond theory and dive into the practical workflow of additive manufacturing (AM) in this hands-on workshop. Participants will be presented with a real-world industrial challenge requiring the production of a component via 3D printing. To solve this problem, attendees will form three specialized, collaborative teams: one focused on material and process selection (evaluating suitable materials based on performance requirements and proper AM process), one on 3D design and simulation (modelling the component for function and manufacturability), and one on 3D printing (slicing, setting up, and running the print). By working together, participants will gain practical insight into the multidisciplinary decisions involved in turning an engineering concept into a manufactured part.
Would My Invention Be Patentable? What Requirements should I Care About?
09:15 - 09:30
12:20 - 13:00
Cytosens Stage

Susana Rodrigues is a Patent Consultant at Inventa and an Engineer with extensive experience in intellectual property and technical sciences. In her current role, she provides strategic patenting advice and solutions to ensure legal protection for innovative creations, building on a career in patent consultation and translation that began in 2015. Her expertise spans multiple technical domains and includes managing complex patent documentation as well as serving as a trainer, auditor, and consultant for numerous laboratories. Many of these facilities are accredited according to ISO/IEC 17025, covering diverse fields from construction materials to metrology. Prior to joining Inventa, she served as Technical Manager at Janz-Contadores de energia, SA (2003–2016) and as a Project Coordinator at ISQ-Instituto de Soldadura e Qualidade (1994–2003), where she managed research and training in high-energy beam technologies. Susana holds both a Master’s in Physical Engineering (2011) and a Bachelor’s in Physical and Materials Engineering (1992) from Universidade Nova de Lisboa. An active member of the Ordem dos Engenheiros, she also served in the Electrotechnics College (2022–2025). Her extensive career and academic background make her a key asset in intellectual property and engineering.
Abstract
This topic covers the fundamentals of patentable inventions and the assessment of whether an idea can be protected by a patent. It explains what qualifies as a patentable invention and examines key patentability requirements: novelty, inventive step (non-obviousness), and industrial applicability (utility). Additionally, the session will highlight common exclusions from patent protection, including abstract ideas, scientific theories, business methods “as such,” and certain medical methods, depending on jurisdiction. Practical examples are used throughout to illustrate what tends to be patentable versus what is usually rejected, helping participants better recognize protectable innovations in real-world scenarios.
09:15 - 09:30
Lunch Time
13:00 - 14:00
09:15 - 09:30
Ciência, Tecnologia e Espiritualidade: Repensar o Propósito Humano no Século XXI
14:00 - 14:40
EDP Labelec Main Stage

Doctor Luís Portela is one of the most respected figures in Portuguese science and in the pharmaceutical sector. A medical doctor by training, he led BIAL for more than forty years, serving as CEO from 1979 to 2011 and Chairman until 2021. Under his leadership, BIAL became the first Portuguese pharmaceutical company to develop and globally commercialise innovative medicines, including pioneering treatments in epilepsy and Parkinson’s disease. In 1994, he founded the BIAL Foundation, today recognised internationally for its support of cutting edge research in neuroscience and in the study of the human condition. He is the author of ten books, two of which are bestsellers, and has been awarded four Honorary Doctorates, as well as several national honours, including the Grand Cross of the Order of Merit and the Grand Cross of the Order of Public Instruction. Doctor Portela has held prominent national roles, such as President of Health Cluster Portugal and Chair of the General Council of the University of Porto. He now dedicates himself fully to the BIAL Foundation, scientific reflection, and the promotion of humanistic thought.
Abstract
Available Soon
09:15 - 09:30
Break Time
14:40 - 14:50
09:15 - 09:30
Construindo um NOVO RH na Era da Inteligência Artificial
14:50 - 15:30
Eurofins Stage

Vanessa Mosca is a recognized HR leader and Artificial Intelligence specialist applying technology to transform business and people management. Co-founder of Promptz, Brazil’s first Prompts as a Service company, she has trained thousands of professionals through her practical and strategic approach to AI adoption in Business and HR. Creator of the first ChatGPT Certification Program in Brazil, she works as an AI consultant, international speaker, and business school lecturer in Brazil and Portugal — helping organizations translate technology into efficiency, innovation, and strategic leadership. Awards: ABTD “HR Personality” Award | International Speaker | Corporate AI Consultant | Lecturer in Business Schools (Brazil & Portugal)
Abstract
Tecnologia e sensibilidade no mesmo palco! Vanessa Mosca é referência quando o assunto é Inteligência Artificial aplicada a RH. No Labsummit 2026, ela traz uma visão afiada e humana sobre inovação, mostrando como a IA pode (e deve) potencializar pessoas.
09:15 - 09:30
Orbit - Transforming Route Management in the Era of Intelligent Operations
14:50 - 15:30
Ambidata Stage

Responsible for leading the design and implementation of the Orbit project, from concept to execution. Focused on aligning operational needs with technological solutions, improving efficiency in field operations, coordinating stakeholders, and driving innovation in route management processes within the laboratory environment
Abstract
The Orbit project is an innovative route management solution designed to optimize field sample collection and laboratory mobility. By leveraging intelligent planning and data-driven decision-making, Orbit improves operational efficiency, reduces travel time, and enhances resource allocation. In this session, we will explore how Orbit addresses logistical challenges in laboratory operations, the methodology behind its development, and the impact it has on streamlining daily workflows. The presentation will also highlight key benefits, real-world applications, and future potential of route optimization in laboratory environments.
09:15 - 09:30
Compliance Como Motor de Confiança: Perspetivas GMP, ISO 9001 e ISO 17025
14:50 - 15:30
Normax Stage
Painel de Compliance
09:15 - 09:30
The Pre-Mortem of Innovation: How to Test Your Next Digital Product Without Spending a Dime
14:50 - 15:30
Inês de Castro

With a deep technical background and an MSc in Information Systems and Technology, Davide uniquely combines engineering expertise with strategic management. Davide excels at bridging the gap between innovative technology and business goals, ensuring that every digital product idea is both technically viable and commercially sound. He specializes in early-stage de-risking, guiding clients through complex architectures and regulatory landscapes in the healthcare sector.

A strong advocate for Human-Centered Design, Edmundo believes that the success of any digital product is decided long before the visual design phase. Edmundo specializes in Digital Product Research and prototyping, transforming complex workflows into intuitive, data-driven interfaces. His mission is to ensure that software actually solves the real-world problems of its users, driving adoption and reducing human error.
Abstract
Did you know that up to 80% of healthcare IT projects fail? Surprisingly, it’s rarely due to bad code. They die because of three invisible killers: Poor Usability, Technical Integration hurdles, and Regulatory traps (like accidentally building a Medical Device). In this highly interactive 40-minute workshop, LOAD will guide you through an "Innovation Pre-Mortem." Together, we will reverse-engineer a fictional lab software disaster to help you identify these fatal flaws early on. Learn how to combine Design Thinking with Technical and Regulatory Assessments (ISO-13485) to stress-test your ideas, de-risk your project, and save your budget before writing a single line of code.
Green Labs: How To Reduce Impact, Increase Resilience, And Gain Efficiency With AI, Compliance, And People-Driven Sustainability
09:15 - 09:30
14:50 - 15:30
Sondar Stage

Filipa holds a Bachelor’s degree in Biology and a Master’s degree in Ecology from the University of Coimbra, as well as a Postgraduate qualification in Sustainability Management from the Higher Institute of Economics and Management. With prior research experience in projects related to Ecosystem Services, she currently works in the fields of environment and sustainability, namely in the areas of Sustainable Finance (Second Party Opinion), Sustainability Reporting and DNSH, Life Cycle Assessment, Carbon Footprint, and Environmental Legislation.
Abstract
Available Soon
Compliance em Solos, Resíduos e Perigosidade: da Amostra ao Resultado
09:15 - 09:30
14:50 - 15:30
Envienergy Stage
Speaker
TBC, Eurofins
Abstrac
Available Soon
Kjeldahl or Dumas? Selecting the Best Reference Method for Protein Analysis
09:15 - 09:30
14:50 - 15:30
Cytosens Stage

Nigar Hajiyeva is an accomplished chemist specializing in polymer chemistry, nanomaterials, and spectroscopic analysis. She currently serves as an International Customer and Application Support Specialist at C. Gerhardt GmbH & Co. KG, where she provides technical expertise and application support to clients and distributors across Europe. She holds a Bachelor’s degree in Chemistry and a Master’s degree in Nanoscience and Nanotechnology. During her Ph.D. studies, her research focused on the synthesis of polymers and the characterization of polymeric nanomaterials. With a solid scientific background and practical experience, Nigar Hajiyeva provides expert support in analysis and customer applications. In her current role, she bridges the gap between laboratory innovation and industrial application, helping customers optimize their analytical processes and achieve reliable results.
Abstract
Fat and fiber determination are essential for assessing animal feed quality. This presentation introduces our advanced systems featuring a fully automated digestion process with innovative filtration technology for fiber analysis, alongside norm-conforming, fully automated hydrolysis and precise fat extraction. Practical examples highlighting accuracy, speed, ease of use, and safety will demonstrate the system's performance in fat and fiber analysis.
09:15 - 09:30
Break Time
15:40 - 16:30
Beyond Integration
09:15 - 09:30
16:30 - 17:10
Eurofins Stage

Electrical Engineer with postgraduate qualifications in Quality Engineering and Integrated Management Systems.
Currently Manager of the Quality, Safety and Sustainability area at EDP Labelec, with a background in laboratory metrology and high‑voltage testing and experience in consultancy and auditing.
Abstract
Integrated management systemshave long been regarded as the end point of organizational maturity for accredited laboratories, providing coherence, traceability and control over technical and accreditation requirements. At the same time, management system standards have evolved towards increasingly integrable, common structures, significantly reducing the complexity of normative integration. In parallel, organizations are adopting transversal, theme‑based governance models supported by functional specialization, raising the question of whether system integration should be seen as a final goal or as a maturity stage enabling alternative organizational approaches. Drawing on EDP LABELEC’s experience, this presentation reflects on how integrated QAS systems interact with transversal organizational models, exploring both opportunities and challenges for ISO/IEC 17025 accredited laboratories, while highlighting critical conditions to preserve role clarity, effective end‑to‑end control and confidence in laboratory processes.
09:15 - 09:30
From Complex Samples To Reliable Data: A New Approach To Microplastics Quantification
16:30 - 17:10
Ambidata Stage

Amparo Fernández Benito holds a PhD in Chemistry and is Business Development Manager at Captoplastic, a company specialized in microplastics quantification and capture technologies in water systems. With a strong technical background in polymer science and analytical methods, she focuses on bridging the gap between laboratory analysis, regulatory needs, and real-world applications. Her work is centered on developing and implementing practical solutions for the quantification of microplastics in complex matrices, supporting laboratories and industries in obtaining reliable and comparable data. Amparo is actively involved in international discussions on microplastics monitoring and regulation, collaborating with water utilities, research institutions, and industry stakeholders to advance the standardization of analytical methodologies.
Abstract
Microplastics analysis has become a growing priority across environmental, industrial, and regulatory contexts. However, most existing analytical approaches are primarily focused on particle identification (e.g., FTIR, Raman), often facing significant limitations when applied to complex matrices such as wastewater or sludge. In these environments, the presence of organic and inorganic interferents, sample heterogeneity, and low comparability between methods make it difficult to obtain reliable and actionable data. As regulatory frameworks evolve, laboratories increasingly require robust, reproducible, and scalable methodologies capable of delivering comparable results across different types of samples. This session presents a novel approach to microplastics quantification based on aggregation, separation, and gravimetric analysis, specifically designed for complex matrices. The methodology enables the determination of microplastics concentration in mass units (mg/L or mg/g), providing a practical and operational metric for laboratory analysis. Importantly, the method is designed for routine laboratory implementation: it is robust, easy to apply, and does not require highly specialized personnel or advanced analytical instrumentation, making it accessible to a wide range of laboratories. Beyond the analytical method itself, the session introduces a complete laboratory workflow — from representative sampling to standardized implementation — allowing laboratories to integrate microplastics quantification into routine analysis. This approach shifts the focus from purely analytical identification towards the generation of reliable, comparable data, supporting both operational decision-making and future regulatory requirements.
09:15 - 09:30
Desafios Associados À Implementação Do Passaporte Digital Do Produto No Setor Metalomecânico
16:30 - 17:10
Normax Stage


Abstract
Empresas e representantes do setor discutem os desafios da rastreabilidade, gestão de dados e novos requisitos europeus associados ao Passaporte Digital do Produto, com Emídio Silvério (Herdmar), João Campos (Silampos) e Pedro Lima (GS1 Portugal), num debate moderado por Cláudia Ribeiro (CATIM).
09:15 - 09:30
Cultura Ética e Compliance: Porque Reforçar A Confiança De Clientes, Parceiros E Sociedade?
16:30 - 17:10
Inês de Castro

Wal Pagoto Chevrand is Compliance & Data Protection Manager at Lusíadas Saúde. She is an experienced healthcare professional with a background in industrial pharmacy and healthcare management. Wal has held senior positions in leading healthcare organizations, specializing in compliance, operations management, and business process improvement. With expertise in implementing compliance programs, ensuring regulatory alignment, and fostering ethical practices, she combines strong technical knowledge with practical leadership.
She has been a Certified Corporate Ethics & Compliance Professional – International since 2015 (Compliance Certification Board) and holds a Postgraduate degree in Healthcare Management from Nova School of Business and Economics. Wal is passionate about promoting integrity, transparency, and sustainable practices in the healthcare sector.
Abstract
Esta sessão abordará a forma como a cultura ética e o compliance vão além do cumprimento dos requisitos regulamentares, reforçando a confiança junto dos stakeholders e da sociedade. Através da análise de falhas reais de compliance e de riscos de corrupção, a apresentação destaca os impactos sociais, reputacionais e empresariais de condutas não éticas. Vamos enfatizar como o papel da liderança, de controlos eficazes e da tomada de decisão ética impactam na construção de Programas de Compliance sustentáveis. Com a avaliação de casos reais vamos demonstrar como a integração de uma cultura ética com uma governação robusta transforma o compliance de uma obrigação legal numa base de confiança, credibilidade e criação de valor organizacional a longo prazo.
Inside the Industry: A 360º Tour From Environmental Control To Product Quality Assurance
09:15 - 09:30
16:30 - 17:10
Sondar Stage

Ana Cristina Gouveia, holds a degree in Environmental Engineering from the Faculty of Biotechnology of the Portuguese Catholic University (UCP) and brings nearly two decades of experience at ISQ – Instituto de Soldadura e Qualidade. She has been a driving force in advancing environmental excellence, laboratory innovation, and sustainable transformation across industries and services. Throughout her career at ISQ, held leadership roles in Commercial Management, Environmental Consultancy, and Business Development, with a focus on Life Sciences and Integrated Laboratory Solutions. Her work bridges science, business strategy, and environmental governance, strengthening credibility, reliability, and performance of analytical laboratories. Her expertise spans environmental legislation and regulatory compliance, pollution control, water and soil quality, waste management, circular economy, sustainability, and environmental governance. She is passionate about fostering trust in laboratory results and environmental data, guiding organizations in building resilient, high-performance testing systems aligned with evolving international standards—from environmental and industrial quality control to the pharmaceutical and oil & gas sectors. Speacker at conferences, workshops, and webinars, actively contributes to the global dialogue on sustainability, regulatory frameworks, laboratory best practices, and scientific reliability, offering a pragmatic and forward-looking perspective on the future of laboratory excellence.
Abstract
Available Soon
09:15 - 09:30
TBC
16:30 - 17:10
Envienergy Stage
Speaker
TBC, Concessus
09:15 - 09:30
TBC
16:30 - 17:10
Cytosens Stage
Speaker
TBC, Labware
09:15 - 09:30
Break Time
17:10 - 17:20
09:15 - 09:30
RA.IA no LabWay-LIMS: do assistente inteligente ao laboratório autónomo
17:20 - 18:00
Eurofins Stage

Carlos Beleza has over 15 years of experience in software development and enterprise information systems. He holds a degree in Computer Engineering and a postgraduate qualification in enterprise applications. Throughout his career, he has contributed to the development and evolution of solutions based on Microsoft technologies and has also led the development team of LabWay-LIMS®. He later took on the leadership of the customer support area in Portugal, driving the transition from a traditional helpdesk model to a consulting-oriented approach focused on customer success. He is currently Commercial Director of Ambidata Group for the Iberian market, with the objective of expanding Ambidata’s solutions across the Iberian market and accelerating the digital transformation of laboratories.
Abstract
A inteligência artificial está a transformar a forma como os laboratórios utilizam os seus sistemas de informação. Nesta apresentação será mostrado como o LabWay-LIMS® integra funcionalidades de IA que tornam a interação com o sistema mais natural e eficiente, incluindo comandos por voz, conversão de voz e texto, apoio na escrita e revisão de conteúdos e simplificação de relatórios técnicos complexos. Será também apresentada a visão de evolução baseada em agentes de IA, capazes de analisar sinais provenientes do laboratório e apoiar na identificação de padrões, antecipação de problemas e tomada de decisão, aproximando o LIMS do conceito de laboratório inteligente e autónomo.
Operational Excellence Strategy In The Nowadays' Labs. Current Drivers And Opportunities To Excel In The Daily Lab Management
09:15 - 09:30
17:20 - 18:00
Ambidata Stage

Dr Javier Martínez del Río is CEO of Tentamus Iberia, where he leads the company’s growth and consolidation as a leading provider of analytical services and quality control in sectors such as food, the environment and industry. He holds a degree in Economics and has several specialist master’s degrees in business management and administration, as well as a PhD that reinforces his solid academic foundation. His career combines scientific expertise, economic knowledge and strategic vision, driving innovation and operational excellence in the laboratory sector.
Alberto Ramentol, Tentamus
Abstract
The industry has faced prolonged market price stagnation and sustained inflationary pressures on costs, including salaries, laboratory supplies, and equipment. These trends have significantly impacted margins, labor relationships and even compromised survival. AS a consequence, laboratory operations in the late 2020s demand a renewed focus on operational excellence to gain efficiency and maintain employee morale. In response, the Tentamus Group in Iberia launched a strategic initiative in 2022 to excel the operational excellence across its laboratories. This session explores the key drivers reshaping Tentamus’ lab management today, from digital transformation and automation to workflow optimization, highlighting the most relevant lessons learned. Attendees will gain actionable insights to lead their teams with clarity, navigate emerging challenges, and position their laboratories as high-performing, future-ready environments
09:15 - 09:30
Painel Normax
17:20 - 18:00
Normax Stage
09:15 - 09:30
Leading the Change: Women in Pharma & Controlled Substances
17:20 - 18:00
Inês de Castro
Painel ISPE/WIP
Abstract
In the pharmaceutical industry and controlled substances sector, women are playing an increasingly important role in driving innovation, strengthening regulatory frameworks, and shaping high-performing organizations. This roundtable brings together voices from Women in Pharma (WIP), the International Society for Pharmaceutical Engineering (ISPE), and professionals across pharmaceutical manufacturing, regulatory affairs, and controlled substances management.
Through shared experiences and expert perspectives, the session will explore leadership, resilience, and the evolving contribution of women in highly regulated environments. By highlighting diverse career paths and perspectives, the discussion aims to foster more inclusive, collaborative, and forward-thinking ecosystems across the industry.
09:15 - 09:30
Ensuring Data Integrity & Compliance In The Digital Lab: Insights And Prevention Strategies
17:20 - 18:00
Sondar Stage

Viktor Kravchuk joined Sartorius in 2021 as an Application Specialist for Lab Weighing in EMEA, focusing on digitalization and automatization processes in the modern labs. Viktor ensures that integrations between different devices and IT systems are carried out in a compliant manner.
Abstract
Data integrity and compliance are critical to reliable laboratory results and remain a key focus for regulators and auditors. The growing reliance on electronic data and computerized systems has introduced new challenges in safeguarding data integrity, particularly for essential instruments like laboratory balances. In this webinar, we’ll draw on examples from FDA warning letters to highlight common compliance issues and demonstrate how a modern laboratory balance - paired with PC software for data storage, maintenance, and analysis - can help prevent them.
09:15 - 09:30
Ergonomics and Performance in Productive Spaces. How Flooring Selection Impacts Efficiency? How to ensure ISO 14644 1 Compliance throughout the lifecycle?
17:20 - 18:00
Envienergy Stage

Pedro Bernardes is Key Account Manager for the Industry segment at Gerflor Iberia, based in Madrid. He has extensive experience in technical solutions for industrial environments, having previously worked in engineering, safety and industrial materials across Iberia. Pedro combines a background in Civil Engineering with more than a decade of experience supporting manufacturing clients with high performance flooring and industrial compliance solutions. He regularly collaborates with engineering firms and end users to optimise ergonomics, safety and technical performance in production spaces.
Abstract
The direct influence of industrial flooring on worker ergonomics, operational efficiency and long term performance in production environments. Often overlooked, the floor is the most used surface in any facility and plays a critical role in fatigue reduction, vibration absorption, slip resistance, safety and overall workflow continuity. The workshop will analyse how different flooring technologies affect operator well being, equipment precision, noise levels, maintenance cycles and the total cost of ownership. Real case studies will illustrate measurable improvements in productivity and ROI achieved through correct flooring specification. Cleanrooms require strict, controlled environments in which every building material contributes to contamination control. Flooring is a critical component that directly affects particle emission, cleanability, electrostatic behaviour, and the facility’s long term compliance with ISO 14644 1. This workshop will provide a full technical overview of how flooring systems influence the cleanroom classification during installation, daily operation and ageing. It will cover typical risks related to wear, joint design, chemicals, biofilm formation and ESD management, as well as strategies to maintain compliance after several years of operation.
Soluções Integradas Para O Controlo Da Qualidade, Automação e Metrologia
09:15 - 09:30
17:20 - 18:00
Cytosens Stage

Filipe Domingues tem uma formação multidisciplinar que alia as ciências da vida à tecnologia. É mestre em Biologia e licenciado em Engenharia Informática pela Universidade Fernando Pessoa, com especialização em Controlo Estatístico do Processo (SPC). Ao longo da sua carreira, passou por funções como programador de aplicações e gestor de projetos, e atualmente é diretor de software, estando diretamente envolvido no desenvolvimento de soluções inovadoras para a indústria.
Abstract
Descubra como as soluções da EGITRON combinam software avançado, metrologia de precisão e automação industrial para transformar o controlo da qualidade. Iremos apresentar casos de sucesso reais que demonstram como nossos sistemas otimizam processos, aumentam a fiabilidade e agilizam as tomadas de decisão críticas na indústria. Uma oportunidade única para conhecer tecnologias integradas que elevam o padrão de excelência na sua operação.
09:15 - 09:30
The Labinox Cocktail Party
18:00 - 19:30
Unwind and Connect at the Labinox Cocktail Reception
After an intensive first day of insights and innovation, it’s time to shift gears! Join us for the Labinox Cocktail Party, the perfect setting to transition from the lecture hall to a more relaxed atmosphere. This evening is all about bringing together our diverse community of participants, speakers, and sponsors to foster new connections and strengthen existing ones.
Enjoy a selection of refreshments and appetizers while our live DJ sets the mood with the perfect soundtrack for conversation. Whether you’re looking to discuss the day’s highlights or simply want to expand your professional network in a laid-back environment, this is the place to be. Let’s raise a glass to a successful start of labsummit!
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