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 9 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 60 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 140 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...

“I accomplished a better understanding on the role of the PRRC. Very knowledgeable [speaker] with a good presentation style.”

Adrian Dunleavy, UK Quality & Regulatory Manager, Freudenberg Performance Materials LP

“I hoped to improve my knowledge in the field of in-licensing and out-licensing agreements. I am completely satisfied. I got answers to my questions, structured my knowledge, received new, previously unknown to me information Everything was great.”

Karīna Kudore, Lawyer, Olpha

“Very concentrated and structured content. All speakers had high level expertise on the topics presented. Useful for in-house practitioners (lawyers, BD) in the pharmaceutical industry as a guide to the main topics in contract drafting. I have expanded my knowledge [on] license agreement issues, IP issues, Co-development agreements.”

Lana Zida, Lawyer, Olpha

“It was well laid out and formatted especially for myself who does not have a regulatory role currently. I was hoping to achieve a firmer understanding and overview of submission within the EU, and believe I achieved this. [Speakers] were very knowledgable and provided great answers to all questions— supportive but challenged us when doing the workshop. I liked all areas of the course.”

Louise Dunn, Pharmacovigilance and Technical advisor, Zoetis

“Excellent. I was hoping to refresh, add to and update my knowledge. The webinar was excellent to remind me of areas that I had been involved with many years ago and add knowledge that is more relevant to my role now. I found the topics of the workshop particularly relevant.”

Mary-Ann Tite, Regulatory Manager, Pets |Choice

“Fantastic webinar! Speakers were very knowledgeable, clear, concise, and open to questions at any time—providing in depth background information were appropriate as well. The content was very interesting and I think a very good amount was covered considering the timescales. I enjoyed the workshop a lot. I thought it was a good way to try and put into practice what we had learnt during the webinars. I also thought a very good amount of information was covered for an introduction into the sections of the dossier.”

Emilija Stabingyte, Regulatory & Quality Coordinator, Zoetis UK Limited

“My goal was to gain a deeper awareness and understanding of what is required in the different sections of a dossier for submission in the EU. I think the course definitely accomplished this and there was lots of useful information, which was very well explained. I can confidently say that I left knowing a lot more than I initially thought I would.”

Emilija Stabingyte, Regulatory & Quality Coordinator, Zoetis UK Limited

“Loved it. Great content, great presenter/instructor. He was engaging and explained things clearly, answering questions along the way. I particularly liked the way he brought the content to life and gave greater insight through sharing examples of his personal experiences. Great course, would recommend.”

Kishori Amatya, PV and MI officer, Jenson R+

“The webinar is well constructed and the speaker is a very polite and prepared person. I managed to get the initial information needed to start studying and understanding the process validation program, the exercises [were] very helpful.”

Alessandra Fanzini, CDMO, REITHERA SRL

“I really enjoyed this webinar. I will be recommending it to colleagues as a great source of information and introduction to process validation. The material was engaging, and [speakers'] knowledge/experience was communicated very well. I greatly enjoyed the content and presentation style. Topics were split up and presented in a logical order and the exercises were very helpful to reiterate the information that was presented.”

Brianna Boehm, Process Validation Technical Writer, Aldevron