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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, pharmacovigilance, 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

Next events:

  • 30-31 Jan 2025 Biosimilars
  • 27-28 Feb 2025 Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products

See all 11 courses

Next events:

  • 6 Dec 2024 Data Integrity and Document Management
  • 20-21 Jan 2025 Clinical Trial Regulatory Requirements

See all 44 courses

GxP

Next events:

  • 6 Dec 2024 Data Integrity and Document Management
  • 13-15 Jan 2025 An Introduction to Pharmaceutical Packaging

See all 57 courses

Next events:

  • 28-29 Jan 2025 Cyber Security for Medical Devices
  • 24-27 Feb 2025 Metered Dose Inhaler (MDI) Technology

See all 20 courses

Next events:

  • 16-17 Jan 2025 Successful Medical Writing – from Protocol to CTD
  • 5 Feb 2025 Effective Technical Writing & Editing

See all 8 courses

Next events:

  • 9-10 Dec 2024 Pharmaceutical Regulatory Affairs in the Middle East
  • 10-11 Dec 2024 Pharmaceutical Regulatory Affairs in China

See all 121 courses

Next events:

  • 9-13 Dec 2024 Advanced Pharmacovigilance
  • 20-21 Jan 2025 Pharmacovigilance QMS & Inspection Preparation

See all 40 courses

Knowledgeable presenters and the presentation decks were well put together.

Leah Conway, Product Development Lead, AGA2tech

I enjoyed the webinar and the content, presentation and speaker was great.

Shelley Browning, Regulatory and PV Manager, Weleda

I enjoyed the webinar and the content, presentation and speaker was great.

Shelley Browning, Regulatory and PV Manager, Weleda

Great course, well spend money and time.

Suada Pieper, Associate Specialist, clinical research, MSD Animal Health Innovation

This was a very well-structured course that can be useful also to people working many years in GCP studies. The content was very interesting and helpful and allowed interaction and questions during the seminar. The excellent speakers are experienced and tried to facilitate all questions raised during the presentations.

Eleni Vatzia, Clinical Research Manager, MSD Animal Health

Excellent. Hoped to achieve better understanding of clinical and quality parts of the dossier and this was very well accomplished.

Päivi Jutila, Regulatory Affairs Manager, Vetcare Ltd

Very content with the course! The length of each chapter was nicely timed, breaks were ideal. The case we studied was a very good way to summarize all the information [seen] and it generated a lot of interesting questions/dilemmas. I would recommend.

Emma Vanmechelen, Regulatory Affairs Specialist, DeLaval

Very informative. Engagaement with participants was great.

Kamila Tomaszewska, RA Specialist, Bausch & Lomb

The content, presentation and speaker were very interesting and clear. They will enable me to improve the management and content of the company's vigilance agreements.

Diarra Ndour , , Innothera Corporate Services – Groupe Innothera

It was a really nice 2 day course. Good variety between information and workshops and the practical tips were usefull. The enthusiasm of the trainers was really nice as well.

Tamara Giesen, Quality Assurance Officer, Royal GD