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In-house & bespoke training:
Life Sciences

The pandemic created numerous challenges across all areas of business worldwide and life science companies responded very quickly. Now, as the healthcare sector emerges stronger and with renewed leadership, the industry can continue to focus on key areas for development and explore ways to challenge existing processes, harness collaborations and build resilience. Our product portfolio has been designed to focus on latest developments and best practice, covering key topics across the pharmaceutical lifecycle, including clinical, regulatory, pharmacovigilance, medical technology, medical writing and biopharma.

 

Sample course outlines include:

  • Biosimilars
  • Biotechnology for the Non-Biotechnologist

See all 2 course outlines

Sample course outlines include:

  • Clinical Evaluation of Medical Devices: The Clinical Evaluation Report
  • Clinical Quality Management Systems

See all 11 course outlines

Sample course outlines include:

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

See all 10 course outlines

GxP

Sample course outlines include:

  • An Introduction to Pharmaceutical Packaging
  • An Introduction to Quality Management for Managers

See all 16 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 Veterinary Vaccine Development and Registration in the EU
  • Advanced Regulatory Affairs for Medical Devices

See all 40 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 10 course outlines

Overall, I would recommend the webinar to people who are starting a career in clinical trials as it gives a good overview of all aspects of GCP.

Laure Bidois, Senior Advisor Regulatory Affairs, knoell

Overall, I would recommend the webinar to people who are starting a career in clinical trials as it gives a good overview of all aspects of GCP.

Laure Bidois, Senior Advisor Regulatory Affairs, knoell

Great content and discussion. Very good presentation style... Very worthwhile presentation

Justine Campbell, Senior Technical Services Veterinaria, QBiotics

Great for anyone looking to build on their PV Vet knowledge - for beginners and more experienced PV professionals especially in line with the new EU Veterinary Regulations

Oluwafemi Odugbesan, , Boehringer Ingelheim Vetmedica GmbH

It was a very useful training that fulfil my necessities about the Industry standards for the Technology transfers... Bruce is very knowledgeable and he was continuously asking the participants to provide feedback and their own experiences.

Sergio Molina Zaragoza, Vice President Research and Development, Grifols Biologicals LLC

It was a well done webinar, the speakers were very competent and experienced. The content was informative

Helena Metzker, Clinical Research Associate, MSD Animal Health Innovation

It was a well done webinar, the speakers were very competent and experienced. The content was informative

Helena Metzker, Clinical Research Associate, MSD Animal Health Innovation

I was hoping to achieve more knowledge about combination product and the regulatory documentations needed for the market authorisation and this was completely accomplished.

Greta Ferrari, Analytical Scientist, Chiesi Farmaceutici

Well designed course that covers the process in the right amount of detail for different delegates, and was very interactive in getting delegates ideas and comments on areas. Presentation was simple and easy to follow given how much there was to cover, and was very well presented from Declan.

Liam Aylwin, Internal Audit Manager, Dechra Pharmaceuticals

Understanding RFP and RFI were achieved, KPI session was very helpful and I learnt about oversight plan which I never knew about... Laura was very good, provided great content of the subject matter and discussions included were good and relevant.

Stephanie Yearwood, Senior Vendor Management Coordinator , IQVIA