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Training courses & Webinars:
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.

 

Next events:

  • 27 Jun-1 Jul 2022 Biotechnology for the Non-Biotechnologist
  • 4-5 Jul 2022 Biosimilars

See all 5 courses

Next events:

  • 4-5 Jul 2022 EU Clinical Trial Regulation 536/2014: Overview and Implementation
  • 7 Jul 2022 Data Integrity and Document Management

See all 17 courses

Next events:

  • 4-5 Jul 2022 An Introduction to the Design and Development of Medical Devices
  • 4-7 Jul 2022 Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations

See all 20 courses

GxP

Next events:

  • 13-14 Jun 2022 An Introduction to Pharmaceutical Packaging
  • 15 Jun 2022 An Introduction to Quality Management for Managers

See all 32 courses

Next events:

  • 15 Jun 2022 Effective Technical Writing & Editing
  • 5-6 Jul 2022 Medical Writing for Medical Devices

See all 7 courses

Next events:

  • 24-25 May 2022 Pharmaceutical Regulatory Affairs in China
  • 25-26 May 2022 Pharmaceutical Regulatory Affairs in Africa

See all 71 courses

Next events:

  • 21-23 Jun 2022 Pharmacovigilance
  • 11 Jul 2022 A Practical Guide to Writing Risk Management Plans (RMPs)

See all 16 courses

Understanding the Pharmaceutical Industry

£150.00/€210.00/$234.00

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