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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, 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

Biopharma

Next events:

  • 4-8 Dec 2023 Biotechnology for the Non-Biotechnologist
  • 6 Feb 2024 Delivery of Biologics to the Nasal Cavity

See all 17 courses

Clinical Research

Next events:

  • 15-16 Jan 2024 Managing Vendor/CRO/CMO Oversight
  • 17-18 Jan 2024 Medical Device Studies: Regulatory Requirements and Adverse Event Reporting

See all 44 courses

GxP

Next events:

  • 16-17 Jan 2024 Process Validation with Qualification
  • 23-24 Jan 2024 Effective Technology Transfer

See all 60 courses

Medical Technology

Next events:

  • 11-14 Dec 2023 Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations
  • 23 Jan 2024 Sustainable Design and Manufacture for Medical Devices

See all 37 courses

Medical Writing

Next events:

  • 1 Feb 2024 Effective Technical Writing & Editing
  • 13-14 Mar 2024 Medical Writing for Medical Devices

See all 9 courses

Regulatory Affairs

Next events:

  • 4-5 Dec 2023 A Regulatory Update on Animal Feed and Feed Additives in the EU, USA and China
  • 11-12 Dec 2023 Medical Device Regulation in the Eurasian Union, Russia and the CIS

See all 136 courses

Vigilance

Next events:

  • 11-15 Dec 2023 Advanced Pharmacovigilance
  • 18 Jan 2024 A Practical Guide to Writing Risk Management Plans (RMPs)

See all 51 courses

In-house training

We can provide any of our courses on an in-house basis - at your location or online, with a programme and presenters tailored to your exact requirements. If you require training for multiple staff members, contact us to see how we can work with you.

Previous attendees said...

“Good speaker and content was very well explained. It met absolutely all my expectations.”

Carmen Lopez, SCIENTIST, IMMUNOCORE

“The content of the webinar was good, thorough. Paul answered any questions which I asked. With clear and concise reasoning. He made it easy to follow and not boring for someone with 4 years stability testing experience and basic knowledge. This has given me the tools I need to go back and hopefully improve the stability studies for the future. I enjoyed, I feel like I'm better prepared to justify the requirements of a stability study to my company. With an understanding of how to reduce costs and apply it to the industry I am in. ”

Elinor Jarvis, Quality Control Team Supervisor, Purolite Ltd

“The webinar was presented very well with both speakers having a clear understanding of the changes and implications that the MDR will have. Both speakers were able to help with all questions with a clear understanding of their answers and applicability. Both speakers were very clear and very helpful with all questions and all parts were very informative, i really liked the workshops. ”

Louise Bateman, Quality Manager, Bedfont Scientific Ltd

“Every item, but especially the topics of signal management & audits and inspections. I am grateful for the advise giving on how to approach audits/inspections.”

Charlotte Lindorf Eriksen, Head of Pharmacovigilance, QPPV, Billev Pharma ApS

“Overall, the speaker was very competent and added a lot of real-world examples and thus enabled better understanding of the theory/regulatory requirements presented. He is an excellent trainer.”

Daniela Bausewein, Associate Director Clinical Safety Management, BioNTech SE

“I really appreciated the rich content of the slides, the level of information provided and the very clear overview of the regulator context, and the roadmaps. ”

Alexia Pleinecassagne, RAQA Specialist, Medimaps Group SA

“Training materials were detailed and easy to follow. Trainer was engaged and made sure that contents were delivered in a way that the Trainees could relate to. ”

Esther Okeudo, QA Specialist, JenaValve

“Training materials were detailed and easy to follow. Trainer was engaged and made sure that contents were delivered in a way that the Trainees could relate to. ”

Esther Okeudo, QA Specialist, JenaValve

“The speaker demonstrated a deep knowledge of all themes presented during the course. Sessions were well organized and enough time was dedicated to each of them.”

Vincenzo Velleca, Global Safety Operations, Zambon SpA

“I certainly have more information after the webinar which set a good foundation for further research. I liked the biopharmaceuticals topics and the packaging slides. These were of particular interest to me. I liked the idea of breakout rooms. A good amount of material was covered over the two days and I enjoyed the idea of breaking up the presentations with exercises.”

Ananthi Ramachandran, Quality Control Manager , Rentschler ATMP Limited