Advance the 3Rs beyond minimum compliance to support organisational change and strengthen responsible research and testing. Learn how the 3Rs (Replacement, Reduction, Refinement) can transform your research. Explore responsible and innovative research methods such as New Approach Methodologies (NAMs), in-vitro and in-silico techniques as well as AI-driven solutions. Develop strategies to reduce animal use through ethical study design, while ensuring scientific integrity.
Steckbrief
- Abschluss
Certificate of Advanced Studies FHNW Strategic 3Rs Implementation in Biomedical Research and Testing- Lernsetting
- Remote und Präsenz
- ECTS-Punkte
- 12
- Nächster Start
- 14.1.2027
- Dauer
- 15 Tage
- Durchführungssprache
- Englisch
- Durchführungsort
- Online und FHNW Campus Muttenz
- Preis
- CHF 6 500 (Early Bird)*
Auf einen Blick
- Develop the knowledge and tools needed to strengthen the implementation of the 3Rs within your professional environment.
- Navigate the ethical and regulatory frameworks governing animal use in research and testing, including ethical review processes and the Harm–Benefit Analysis.
- Evaluate the suitability of alternative approaches, including New Approach Methodologies (NAMs), to replace or complement animal models in different research and testing contexts while taking regulatory acceptance into account.
- Design research strategies that minimise animal use through improved study design, statistical planning and refinement practices that enhance both animal welfare and scientific quality.
- Enhance organisational good practices in research and testing through stakeholder engagement, effective communication, and change-oriented approaches.
Ziele und Nutzen
The CAS Strategic 3Rs Implementation in Biomedical Research and Testing focuses on how the principle of Replacement, Reduction and Refinement (3Rs) can be strategically implemented within research organisations. The programme explores the evolving landscape of scientific methods, including new strategies for reduction and refinement as well as replacement approaches such as New Approach Methodologies (NAMs), and examines how these innovations can be integrated into research and testing practice.
Researchers and institutional stakeholders increasingly face complex questions when applying the 3Rs in practice. Beyond the scientific foundations, the CAS addresses the regulatory, organ-isational and institutional contexts that shape 3Rs adoption. The programme equips participants with the knowledge and analytical tools to navigate implementation challenges - such as deci-sion-making processes, governance structures and barriers to adoption - and to advance the 3Rs beyond minimum compliance, using them as a comprehensive framework for guiding good and responsible research practice within research organisations.
This CAS is structured in 6 modules, which can be attended individually or as part of the full cer-tificate programme. Please contact us directly for availability and pricing options of individual modules.
Successful completion of all 6 modules leads to the Certificate of Advanced Studies. Modules completed individually are fully recognised toward the CAS qualification, and participants have up to four years to complete the remaining modules and obtain the CAS.
Zielpublikum
This part-time programme is designed for professionals who operate at the interface of regulation, science and institutional practice who are seeking practical ways to advance 3Rs implementation beyond minimum compliance and integrate them more strategically within their organisations.
It is particularly suited for professionals involved in animal experimentation and its governance in research institutions, universities, regulatory bodies and public authorities, as well as in the pharmaceutical, biotechnology, chemical and consumer goods industries.
The programme is especially relevant for:
- Heads and managers of animal facilities
- 3Rs officers, animal welfare officers and designated veterinarians
- Members of cantonal animal experimentation committees and veterinary authorities
- Preclinical and translational researchers
- Study directors, principal investigators and senior scientists
- Research strategy, governance and compliance professionals
- Regulatory affairs professionals
The admission criteria are outlined below.
Aufbau und Inhalte
The programme combines theoretical input with real-world case studies and practical examples. Participants gain insight into the ethical context of animal use in research, legal and regulatory frameworks, as well as the implementation of the 3Rs in research organisations. Moreover, comprehensive modules address the most advanced 3Rs methodologies are covered, from replacement technologies such as in vitro methods, in silico modelling and AI-supported approaches, to addressing practical strategies for reducing animal use through improved study design and statistical methods, as well as refinement approaches that enhance both animal welfare and experimental quality.
These topics are explored within a broader European context in which the implementation of the 3Rs is rapidly evolving. Switzerland plays a leading role in advancing the scientific and regulato-ry implementation of the 3Rs. Developed in collaboration with the Swiss 3R Competence Centre and European 3Rs organisations, this CAS is embedded in a strong network of research institutions, regulatory authorities, and industry stakeholders working to advance responsible research and testing. Participants benefit from direct engagement with international experts and from insights into current European developments shaping the future of alternative methods and 3Rs implementation.
Teaching methods include on-site and online lectures, guided reading, quizzes, demonstrations and applied case analyses. Participants will apply the knowledge gained to a case study of their choice, examining a real-world challenge related to 3Rs implementation and presenting their in-tegration strategy in a final written assignment.
Module 1: Introduction to the 3Rs and ethical aspects of animal use in research, education and testing (1 day)
Module 2: Legal and regulatory frameworks governing animal use and alternative methods (2 days)
Module 3: Replacement strategies: integrating alternative approaches (4 days)
Module 4: Reduction strategies: Designing studies that minimise animal use (2 days)
Module 5: Refinement strategies: improving animal welfare and scientific quality (2 days)
Module 6: Advancing 3Rs implementation in research organisations (3 days)
Voraussetzungen und Zulassung
At least one of the following admission requirements must be met:
- Tertiary A: University degree (at least a Bachelor’s degree) and, usually, at least 2 years of relevant professional experience or
- Tertiary B: Federal Diploma of Higher Education (“Höhere Fachschule” or “eidg. HFP” or “eidg. BP”) and usually at least 5 years of relevant professional experience or
Individuals without a Tertiary A or B qualification may be admitted if they meet all of the following criteria: At least 10 years of professional experience in a field relevant to the programme, including at least 5 years in a (specialist) leadership role, evidence of other qualifications (e.g. various non-formal, extensive continuing education or partial completion (>50%) of a tertiary-level qualification) and proof of acquired knowledge of academic/scientific work, or willingness to acquire this knowledge in advance.
As the instruction and training materials are in English, proficiency in English (minimum level C1) is a prerequisite.
Organisatorisches
Unterrichtsform
Preis
Programmpartner
Downloads
Beratung und Info-Anlässe
Kontakt
Prof. Dr. Laura Suter-Dick
- Telefon
- +41 61 228 56 59
- laura.suterdick@fhnw.ch
Info-Anlässe
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Anmeldung
CAS Strategic 3Rs Implementation in Biomedical Research and Testing14. Januar 2027
- Datum
- 14.1.2027
- Ort
- Online und FHNW Campus Muttenz
- Kursleitung
- Prof. Dr. Laura Suter-Dick
- Anmeldeschluss
- 4.12.2026