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In-house & bespoke training:
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

Sample course outlines include:

  • Biosimilars
  • Biotechnology for the Non-Biotechnologist

See all 5 course outlines

Sample course outlines include:

  • Advanced Project Management in Clinical Research
  • Clinical Evaluation of Medical Device Software

See all 16 course outlines

GxP

Sample course outlines include:

  • An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices
  • An Introduction to ISO 11607 - Packaging for Terminally Sterilized Medical Devices

See all 31 course outlines

Sample course outlines include:

  • An Introduction to the Design and Development of Medical Devices
  • Cyber Security for Medical Devices

See all 12 course outlines

Sample course outlines include:

  • Effective Technical Writing & Editing
  • Medical Writing for Medical Devices

See all 3 course outlines

Sample course outlines include:

  • Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers
  • A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products

See all 60 course outlines

Sample course outlines include:

  • A Practical Guide to Producing and Maintaining the PSMF
  • A Practical Guide to Writing Risk Management Plans (RMPs)

See all 17 course outlines

Webinar was excellent, very enjoyable and learned a lot of statistics.

Siobhan Crowe, Operation Manager, Univet Ltd

Very clear, interesting and worth it!

Mélissa Cardenas Trujillo, Regulatory Affairs & Registrations Specialist I, Laboratoires Thea Sas

Excellent, this is the second course I have attended run by IPI academy.

Huw Evans, Medical & Scientific Liaison, Mitsubishi Tanabe Pharma Europe Ltd

Content was great. Speaker was wonderful!

Elsje Du Preez, Manager Vendor Management & Administration, Hillevax GmbH

Overall, the course was really good, the speakers were of a very high standard and knew their stuff super well. This really shone through their examples and diverse experience in pharmaceuticals.

Yasmeen Scotto, QA Validation Associate, Catalent Micron Technologies Limited

Overall, the course was really good, the speakers were of a very high standard and knew their stuff super well. This really shone through their examples and diverse experience in pharmaceuticals.

Yasmeen Scotto, QA Validation Associate, Catalent Micron Technologies Limited

Really good. Very thorough. Well constructed in a way that allows the presentation to be used as a reference doc later. The speaker was excellent.

David Bellars, Supply Chain Manager, Cycle Pharmaceuticals Ltd

In general, I was very satisfied with this webinar, I learned a lot.

Jasmina Roca, QPPV deputy, Isdin

Excellent! Exactly what I was hoping for

Mona Bjørkmo, Associate Director, Drug Safety & Risk Management, GE HealthCare

A good presentation with lot of examples. The speaker is well versed with the topic and pharmacovigilance practices.
All other non-signal questions were also answered. Appreciate that

Sanam Chandwani, Manager Aggregate reports, Accord Healthcare