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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:

  • 25-27 Sep 2024 Biotechnology for the Non-Biotechnologist
  • 17-18 Oct 2024 Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products

See all 13 courses

Clinical Research

Next events:

  • 16-17 Sep 2024 Clinical Trial Regulatory Requirements
  • 16-17 Sep 2024 Medical Device Studies: Regulatory Requirements and Adverse Event Reporting

See all 54 courses

GxP

Next events:

  • 3-4 Oct 2024 Development of Combination Products: Critical Interactions
  • 7-8 Oct 2024 Effective Technology Transfer

See all 71 courses

Medical Technology

Next events:

  • 9-10 Oct 2024 Metered Dose Inhaler (MDI) Technology
  • 15-16 Oct 2024 Cyber Security for Medical Devices

See all 32 courses

Medical Writing

Next events:

  • 1 Oct 2024 Effective Technical Writing & Editing
  • 25-26 Nov 2024 Medical Writing for Medical Devices

See all 9 courses

Regulatory Affairs

Next events:

  • 18 Sep 2024 EU Proposed Pharmaceutical Legislation Changes
  • 24 Sep 2024 The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR

See all 158 courses

Vigilance

Next events:

  • 18-20 Sep 2024 Advanced Pharmacovigilance
  • 26-27 Sep 2024 Pharmacovigilance QMS & Inspection Preparation

See all 54 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...

“Fantastic, energetic, and positive. Very clear describing of the topics and good structure. Discussions. It made me feel more involved in the webinar. ”

Viktoriia Kyrylenko, Project Manager, BIOPHARMA PLASMA LLC

“Great knowledge of the material. Great speaker. I liked when the speaker gave insights into what will be expected of manufacturers and what legislation or publications are coming down the line and also his insights into the future ”

Denise McDermott, Regulatory Compliance Team lead, Compliance and Risks

“Koen is a great speak who explains things very clearly with examples ”

Yisong Yin, Software Regulatory Affairs Specialist, Convatec

“Koen is a great speak who explains things very clearly with examples ”

Yisong Yin, Software Regulatory Affairs Specialist, Convatec

“Good speaker, clearly very knowledgeable in the area. He was happy to have conversations about any specific scenarios/examples/questions we had.
Very friendly and i applaud his speaking almost continuously on this topic for two days”

Michaela Hume, Engineer, 42 Technology

“The speaker was knowledgeable, and made an effort to incorporate videos & discussions to break up a dry subject. ”

Beatrice Millward, Data Manager, Liverpool Clinical Trials Centre - University of Liverpool

“David was a very good presenter in going through the content in detail and made it easy to follow. Great with regards to answering questions people had. Very good webinar for all aspects, would recommend to others”

Simran Sandhu, R&D Scientist, Medtrade Products Limited

“Overall the course was good. ”

Ervin Javier Obnial, Validation Specialist, ViroCell Biologics

“Very patient and understanding of everyone's different experience in the industry. Very good course, lots of detail provided, all questions were answered with detail and understanding. I enjoyed the examples provided for the principles (e.g. what went right and what went wrong). Also enjoyed the collaborations with other participants.”

Luissana Vidal, Principal Validation Specialist, ViroCell Biologics Ltd

“Very good, lots of relevant material and clearly outlined. ”

Kurt Blinston, R&D Manager, Medtrade Products Ltd