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

See 1 course outline

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 53 course outlines

Pharmaceutical

Sample course outlines include:

  • Risk Management for Clinical Research
  • A Practical Guide to Producing and Maintaining the PSMF

See all 98 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...

“Knowledgeable presenters and the presentation decks were well put together. ”

Leah Conway, Product Development Lead, AGA2tech

“I enjoyed the webinar and the content, presentation and speaker was great.”

Shelley Browning, Regulatory and PV Manager, Weleda

“This was a very well-structured course that can be useful also to people working many years in GCP studies. The content was very interesting and helpful and allowed interaction and questions during the seminar. The excellent speakers are experienced and tried to facilitate all questions raised during the presentations. ”

Eleni Vatzia, Clinical Research Manager, MSD Animal Health

“Excellent. Hoped to achieve better understanding of clinical and quality parts of the dossier and this was very well accomplished. ”

Päivi Jutila, Regulatory Affairs Manager, Vetcare Ltd

“Very content with the course! The length of each chapter was nicely timed, breaks were ideal. The case we studied was a very good way to summarize all the information [seen] and it generated a lot of interesting questions/dilemmas. I would recommend.”

Emma Vanmechelen, Regulatory Affairs Specialist, DeLaval

“Great course, well spend money and time. ”

Suada Pieper, Associate Specialist, clinical research, MSD Animal Health Innovation

“Really fantastic and loved the speakers keep all the delegates engaged. Especially not being a native English speaker, i really enjoyed the [time taken] throughout the session, which was very practical in day to day work as medical writer”

RamaKrishnaChaitanya Aluri, Medical Writer, Novonordisk

“Very informative. Engagaement with participants was great.”

Kamila Tomaszewska, RA Specialist, Bausch & Lomb

“The content, presentation and speaker were very interesting and clear. They will enable me to improve the management and content of the company's vigilance agreements.”

Diarra Ndour , , Innothera Corporate Services – Groupe Innothera

“It was a really nice 2 day course. Good variety between information and workshops and the practical tips were usefull. The enthusiasm of the trainers was really nice as well.”

Tamara Giesen, Quality Assurance Officer, Royal GD