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vetklinfo – Your Gateway to Clinical Research
Practice-oriented early-career training in clinical research and regulatory affairs, aligned with academic and industry standards.
Regulatory expertise can open doors to careers in the pharmaceutical industry and regulatory authorities.
Our seminars provide practical insights into how medicinal products are developed, tested, authorised and monitored.
Benefit from our experience delivering seminars in collaboration with universities, training academies and pharmaceutical companies.
Target Audiences
Students
Are you studying veterinary medicine or life sciences, pursuing a doctorate, or considering a career in the pharmaceutical industry or at a regulatory authority? A sound understanding of regulatory requirements can help you get started and strengthen your professional profile early on.
Graduates
Have you completed your degree or doctorate and want to career prospects in clinical research or regulatory affairs improve? Our seminars offer practical knowledge of processes, requirements and key interfaces within the pharmaceutical industry.
Professional Development
Are you already working in the field or preparing for a role in clinical research or regulatory affairs? Develop your expertise through practical training focused on current regulatory and industry requirements.
Why Choose vetklinfo Seminars?
Practical, Not Just Theoretical
Regulatory principles are linked to real processes, cross-functional interfaces and examples from the pharmaceutical industry and clinical research.
Current and Industry-Focused
Our content reflects current regulatory requirements and issues relevant to universities, training academies and pharmaceutical companies.
Clear, Structured and Focused
Complex regulatory topics are explained clearly and systematically, with a focus on professional practice.
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Our Seminars
Good Laboratory
Practice
Non-clinical safety studies are planned, conducted and documented in accordance with GLP. They provide essential data for subsequent medicinal product development.
Good Clinical
Practice
Clinical trials evaluate efficacy and safety under defined quality requirements. The resulting data are an essential component of the marketing authorisation process.
Good Vigilance
Practice
After authorisation, medicinal products are continuously monitored for risks and emerging safety signals. The focus is on ongoing benefit–risk assessment.
Authorisation of
Veterinary Medicines
This seminar explains, step by step, the regulatory authorisation of a medicinal product candidate through to a market-ready product and the challenges involved, using practical examples.
Alternatives
to Animal Testing
Animal experiments raise ethical questions and are not equally informative for every scientific question. The seminar examines the potential and limitations of alternative methods .
Clinical
Pharmacology
The pharmakokinetischen, pharmakodynamischen aspects of veterinary and human medicinal product development are explained in accessible terms.
Your Trainer
Dr. Stefan Lindner
Dr Stefan Lindner is a licensed veterinarian who earned his doctorate in veterinary pharmacology and toxicology at Leipzig University. He was awarded a scholarship by Bayer Vital Animal Health and has taught regulatory affairs and clinical trials for more than a decade in both the veterinary and human pharmaceutical sectors.
vetklinfo has an established network in academic and industry training and collaborates with partners including ATV GmbH, Pharmaakademie and Hardenberg Consulting .
He maintains up-to-date expertise through regular continuing education and attendance at specialist events. Selected examples are listed under “Selected Training Courses and Specialist Events”.
Selected Clients and Institutions
- In-house training for pharmaceutical companies (z.B. laPharm, Sanofi, Verovaccines, Bracco, SaluVet GmbH)
- Pharmaakademie, throughout Germany: pharmaceutical sales representatives and medical device advisors (IHK)
- Pharmaakademie, throughout Germany: regulatory affairs for veterinary and human medicines for Clinical Research Associates (CRAs) and Medical Science Liaison Managers (MSLs)
- ATV Life Science Management, Leipzig and Munich: Regulatory Affairs
- ZKS, Centre for Clinical Studies, Leipzig University: Masterstudiengang Translationale Medizin
- Biotechnology Students’ Initiative (registered association): Berlin, Cologne, Münster, Ulm, Braunschweig, Lübeck, Regensburg, Stuttgart, Heidelberg, Göttingen, Dresden and Bochum
- GRADE, Graduate Academy of Goethe University Frankfurt
- Department of Cardiothoracic and Vascular Surgery, University Medical Center Göttingen
Selected Training Courses and Specialist Events
- 18.08.2026: Berlin Institute of Health, Charité: Organoid Intelligence: Exploring Brain Organoids and Artificial Intelligence
- 29 April 2026: Saxony State Chamber of Veterinarians: Vaccination – Current Developments and Challenges
- 14.04.2026: Berlin Institute of Health, Charité: Cancer-SOLES: A Systematic Online Living Evidence Summary of Preclinical Cancer Research
- 03.02.2026: Berlin Institute of Health, Charité: Multi-center preclinical trials, a novel approach in the drug discovery pipeline to enhance translation
- 15.-17.01.2026: Leipzig Veterinary Congress
- 30.11.2025: Knoell Academy: Expert insights into choosing and becoming an Investigator Site for veterinary clinical trials
- 25.09.2025: medfiles: EU VMP Regulation from the perspective of variations and the quality part of the pharmacovigilance system
- 18.09.2025: 21. VAAM Industry-Academia Panel: In Vitro Microbiome Models
- 17.09.2025: Knoell Academy: Accelerating global animal health product development & registration
- 05.06.2025: Pharmaakademie: GCP under the German Medicines Act for clinical trial team members under Regulation (EU) 536/2014 (human medicinal products)
- 19.09.2024: 15th VAAM Industry-Academia Panel: Next generation transformation - bioportides for gene delivery in various eucaryotic and procaryotic microorganisms
- 18.01.2024: 11th VAAM Industry-Academia Panel: different approaches in academia and industry lead to next generation enzymes
- 14.12.2023: IMPSS Early Career Investigators Interest Group: Start ups within microphysiological systems field
- 20.07.2023: 8. VAAM Industry-Academia Panel: Recent advances in phage drug development & application
- 25.08.2022: Landestierschutzbeauftragte Berlin, SenJustVA: Expert Panel Discussion on the Future of Science in the EU & Beyond
- 06.07.2022: Knoell Academy: Pharmacovigilance - Moving to the new signal management system
- 19.05.2022: Deutsches Primatenzentrum: 3Rs in (inhalation) drug research
- 06.05.2022: akademie.vet: The new EU Veterinary Medicinal Products Regulation
- 31.01.2022: Knoell Academy: Veterinary Studies - A European Perspective
- 29.01.2022: Knoell Academy: Distribution arrangements for API´s 2019/6 Art.95
- 28.01.2022: Knoell Academy: Limited Markets in Regulation 2019/6
- 23.08.-02.09.2021: World Congress on 3R’s: Alternatives to animal research from development to application
- 01.-14.09.2021: Johns Hopkins University: Toxicology 21: Scientific Applications
- 30.07.2021: Clinevo: eTMF- Live Training Program and Certification
- 29.07.2021: EMA: Clinical Trials Information System (CTIS)
- 14.06.2021: Pharmaakademie: Dozentenweiterbildung - Online tools / digital training
- 30.03.2021: Proderm Seminar: Medical device or medicinal product?
- 18–20 February 2021: Academy for Continuing Veterinary Education: Qualification as an animal welfare officer
- 24.03.2020-28.02.2021: BVL: Symposium Herausforderungen 2020 - Antibiotics module