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 59 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...

“The course was very interesting and detailed. I'm very new to medical devices and I would have benefitted from an introductory course first. However, I have the tools I need to find answers to questions I might have.”

Afi Sinclair, Regulatory Affairs Consultant, SincasPharma

“Very dynamic and engaging presentations. I wanted to gain a general understanding of the structure of the Chinese agency and its various functions, as well as the overall process for finished product registration. I’m truly pleased with the information that was shared — it fully met my expectations. The materials were very comprehensive, containing a wealth of information on the topic and very well organized. The speakers were highly knowledgeable and had a broad perspective on the topic. It was very interactive, making participation easy and encouraged. The platform was excellent in facilitating communication during the presentation. ”

Montserrat Megias Barrera, RA Manager, inke

“This was a comprehensive webinar training that met my expectations: highly illustrated with examples, interactive, enabling experience sharing with other attendees. All parts were complete and great speaker. I really appreciated the introduction of tools and templates that are helpful.”

katia Hay, Clinical trial coordinator, Adocia

“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

“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

“Great. I particularly liked the global information [section] and it was up to date information so I thought it was really complete.”

Maya El Fayoumi, Chargée Affaires Réglementaires, Panpharma Ltd

“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