In-house & bespoke training:
Industry

 

Please note: full product details will be shown on our training portal IPI Academy where you can find out more and book

Animal Health

Sample course outlines include:

  • A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products
  • A Practical Approach to Veterinary Vaccine Development and Registration in the EU

See all 10 course outlines

Biopharma

Sample course outlines include:

  • US FDA - Understanding Key Factors When Working with the FDA

See 1 course outline

Cosmetics

Sample course outlines include:

  • Cosmetovigilance
  • Regulatory Compliance and Safety Standards for Aesthetic Devices

See all 2 course outlines

Medical Devices

Sample course outlines include:

  • A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK
  • Advanced Regulatory Affairs for Medical Devices

See all 58 course outlines

Pharmaceutical

Sample course outlines include:

  • A Practical Guide to Producing and Maintaining the PSMF
  • A Practical Guide to Writing Risk Management Plans (RMPs)

See all 133 course outlines

Training options

All of our course outlines are available:
Ready made for any number of participants or With a programme and presenters customised to your requirements
And in your preferred format, or combination:
Face-to-face training at your location or Webinar/interactive online

Previous attendees said...

“Overall, this is a good seminar. It is a little long, but that is to be expected looking at the contents and countries to be covered. 5* - I would recommend.”

Kong Kong Weng-Yip, Assistant Manager RA, DUOPHARMA (M) SENDIRIAN BERHAD

“All good! I learn quite some insights. As a researcher I was unsure if I would understand the content of the course entirely, but I did not have any problem; plus, I learned new tools and techniques that I will definitely implement. 5* - I would recommend. ”

Clara Vázquez García, Immunology Dept., Max Delbrück Center

“Overall, it was a wonderful webinar and has helped me further expand my knowledge on the EU/UK regulations. I look forward to participating in future webinars.”

Iva Martinovic, Medical Information Professional, Teva

“My expectation was to gain as much knowledge as possible about EAEU regulations. It was very helpful and useful to get EAEU region overview and understand regulatory approach in each country.”

Maryna Orudzheva, Regulatory Manager CIS, Accord Healthcare Polska Sp. z o.o.

“Very knowledgeable [speaker, who] brought the course to life by dipping into her own experiences of some scenarios which made the course very relatable. ”

Derek Lilley, National Account Manager, Colonis Pharma Ltd

“Very good seminar which covered all important points around the production and maintenance of the PSMF. The speaker was excellent with a profound knowledge of the topic.”

Marie-Christine Klös, Global PV Specialist, Boehringer Ingelheim Vetmedica GmbH

“Very Good. I wanted to get an overview of EU Pharmaceutical Regulations and to understand regulatory strategies to bring new products quickly into the market. The course covered everything I needed and even more. ”

Chitra Saxena, Senior Manager Regulatory Affairs, Lupin Healthcare (UK) Limited

“It was very useful to have specific ideas, tools, websites and portals introduced as to what should be done for CRO oversight.”

Kenji Tada, Unit Manager, Clinical Operation Unit, JCR Pharmaceuticals Co

“Very good. [Speaker was] very experienced.”

Celine Anselmetti Dayer, Director, Regulatory Affairs, Debiopharm Research & Manufacturing SA

“Very good.”

Peter Wæde Hansen, Senior International Medical Manager, Novo Nordisk AS