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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 17 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 32 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:

  • 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 61 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

Excellent content and great detailed presentations.

Michele Power, Global Pharmacovigilance Alliance Manager, Otsuka

Great webinar, content and speaker

Janine Gavin, Director, Collaborative Pharma Ltd

Very helpful, practical and of high quality.

Delphine Decrouy, Regulatory affairs Manager, Axience

The webinar was great!!!

Miguel Angel Ramirez Arredondo, Regulatory Affairs Manager, Sanfer Salud Animal

Informative webinar. Recommend to those wanting to know/validate current industry practices/thinking.

Alesia Mitchell, Associate Director, Global AH PV and RA Quality Standard, Boehringer Ingelheim Animal Health

It was excellent.

María Jesús Bermejo San Román, , Pharma Mar, S.A.

Very detailed and informative.

Antonella Fusco, PV Medical Function, ALFASIGMA SPA

The overview was great, information clear and shared with links.

Ana Karla Uribe Rivera, Research Fellow of Image Guided Surgery, IHU, Strasbourg

Thumbs up. Very information and detailed. Would recommend to colleagues and friends working in the area.

Rukhsana Sofia, Pharmaceutical Affairs Manager, Aspen Healthcare FZ LLC

Very comprehensive.

Cláudia Medeiros, International Head of Regulatory Affairs, Pharma Bavaria Internacional (PBI)