Training courses & Webinars:
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Next events:

  • 2-3 Oct 2024 Introduction to Veterinary Pharmacovigilance
  • 9-10 Oct 2024 Advanced Veterinary Pharmacovigilance

See all 6 courses

Next events:

  • 27 Nov 2024 US FDA - Understanding Key Factors When Working with the FDA

See 1 course

Next events:

  • 14-15 Oct 2024 Cosmetovigilance

See 1 course

Next events:

  • 10 Jul 2024 Smart Packaging and Electronic Patient Information
  • 22-25 Jul 2024 Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations

See all 41 courses

Next events:

  • 4-5 Jul 2024 Agile Leadership for Pharma and Biopharma Professionals in a hybrid world
  • 8-9 Jul 2024 Drafting Commercial Contracts for the Pharmaceutical Industry

See all 95 courses

Very instructive webinar. Although packed, the day went by quickly.

Ariane Teyssou, Regulatory Affairs Specialist, Enterome

Jonathan was a really good speaker and took his time to answer any of our questions. He was very knowledgeable.

Henry Bland, QARA Specialist, Adtec Healthcare

Jonathan was really very excellent.
Clearly has a thorough understanding of the FDA and is able to impart that knowledge incredibly well.
The slides were extensive (Jonathan clearly put a lot of time and effort into these) and will be a great resource for me in the future.

Vikki Young, Head of Quality and Regulatory, Prothea Technologies

This course is very informative and interactive and touched all aspects off Medical device approval process by FDA. Overall excellent, webinar logistics are surprisingly easy, Jonathan's presentation of FDA content is exemplary. Jonathan is a great educator and shared all his experiences.

Sai Prasad, Global Clinical & Medical Advisor, Surgical Structural Heart, Edwards Lifesciences Corp

I was hoping to learn about the reg process for companion animals - the course more than delivered on this!

Scott J. Roberts, Reader in Translational Skeletal Research, Royal Veterinary College

I was hoping to gain a better understanding of the US approval process as I currently work on EU registrations but am moving to a more global role. The webinar covered the US process really well and I don't feel there was anything missed.

Susan Scanlan, Regulatory Affairs Scientific Leader - CMC, Dechra Limited

Excellent speakers. Very knowledgeable. Gave practical and realistic interpretation of current MD activity in the MENA region.

Naomi Smith, Regulatory Affairs Specialist, STERIS

I think Jonathan was really knowledgeable and had an easy way to explain things. Very graceful and humble teacher, including everyone and making all feel ok to ask questions.

Christina Dahl, Regulatory Affairs Associate , Cencora

Nice training with committed speakers, participants were involved. Content is dense but well explained.

Anne Trotel, Clinical Project Manager, Ceva Animal Health

The speakers were highly engaging and delivered the content in an interactive manner, which greatly enhanced the learning experience. Their expertise and ability to facilitate discussion made the webinar both informative and enjoyable.

Dania Shriki, REGULATORY AFFAIRS OFFICER, Owlpharma Consulting, Lda.