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Training courses & Webinars:
Life Sciences

Our life sciences training courses cover Pharmaceuticals, Medical Devices, IVDs, Biotech/Biopharma and Animal Health and have been designed to focus on regulatory affairs, clinical trials, pharmacovivilance, medical writing, latest developments, and best practices (GxP).  Our portfolio of events is extensive and provides training from basic to advanced levels in a variety of formats.  

The pandemic created numerous challenges across all areas of business worldwide and companies had to respond and adapt very quickly. Now, as the healthcare sector emerges stronger and with renewed strategy, life science companies continue to focus on key areas for development, explore the use of emerging technologies, and seek opportunities to harness collaborations and build resilience. 

 

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

Biopharma

Next events:

  • 10-11 Jul 2024 Biosimilars
  • 25-27 Sep 2024 Biotechnology for the Non-Biotechnologist

See all 7 courses

Clinical Research

Next events:

  • 11 Jul 2024 Metrics and Earned Value in Clinical Research Projects
  • 22 Jul 2024 Data Integrity and Document Management

See all 19 courses

GxP

Next events:

  • 10 Jul 2024 Smart Packaging and Electronic Patient Information
  • 11-12 Jul 2024 Stability Testing of Pharmaceuticals and Biopharmaceuticals

See all 23 courses

Medical Technology

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 15 courses

Medical Writing

Next events:

  • 1 Oct 2024 Effective Technical Writing & Editing
  • 21-22 Nov 2024 Medical Writing for Medical Devices

See all 3 courses

Regulatory Affairs

Next events:

  • 18 Jul 2024 Best Practice for Writing Effective SOPs
  • 19 Jul 2024 CAPA (Corrective and Preventative Action)

See all 52 courses

Vigilance

Next events:

  • 8-9 Jul 2024 Understanding Pharmacovigilance Regulations in APAC
  • 10 Jul 2024 Pharmacovigilance Aspects of Licensing Agreements

See all 18 courses

In-house training

We can provide any of our courses on an in-house basis - at your location or online, with a programme and presenters tailored to your exact requirements. If you require training for multiple staff members, contact us to see how we can work with you.

Previous attendees said...

“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.