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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

Biopharma

Next events:

  • 9-11 Jul 2025 Biotechnology for the Non-Biotechnologist
  • 30 Sep-1 Oct 2025 Biosimilars

See all 5 courses

Clinical Research

Next events:

  • 7 Jul 2025 GCP and Clinical Research Update - Hot Inspection Topics
  • 14 Jul 2025 Data Integrity and Document Management

See all 18 courses

GxP

Next events:

  • 7-8 Jul 2025 The Common Technical Document
  • 9-10 Jul 2025 Understanding Computer System Validation (CSV)

See all 24 courses

Medical Technology

Next events:

  • 21-22 Jul 2025 Pre-Filled Syringes: End-to-End Processing
  • 11-12 Sep 2025 Cyber Security for Medical Devices

See all 8 courses

Medical Writing

Next events:

  • 25-26 Sep 2025 Successful Medical Writing – from Protocol to CTD
  • 30 Sep 2025 Effective Technical Writing & Editing

See all 3 courses

Regulatory Affairs

Next events:

  • 9-10 Jul 2025 Understanding Computer System Validation (CSV)
  • 10-11 Jul 2025 Medical Device Single Audit Programme (MDSAP)

See all 45 courses

Vigilance

Next events:

  • 7-8 Jul 2025 Signal Detection and Regulatory Expectations
  • 11 Jul 2025 A Practical Guide to Writing Risk Management Plans (RMPs)

See all 14 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...

“The course was very interesting and detailed. I'm very new to medical devices and I would have benefitted from an introductory course first. However, I have the tools I need to find answers to questions I might have.”

Afi Sinclair, Regulatory Affairs Consultant, SincasPharma

“Very dynamic and engaging presentations. I wanted to gain a general understanding of the structure of the Chinese agency and its various functions, as well as the overall process for finished product registration. I’m truly pleased with the information that was shared — it fully met my expectations. The materials were very comprehensive, containing a wealth of information on the topic and very well organized. The speakers were highly knowledgeable and had a broad perspective on the topic. It was very interactive, making participation easy and encouraged. The platform was excellent in facilitating communication during the presentation. ”

Montserrat Megias Barrera, RA Manager, inke

“This was a comprehensive webinar training that met my expectations: highly illustrated with examples, interactive, enabling experience sharing with other attendees. All parts were complete and great speaker. I really appreciated the introduction of tools and templates that are helpful.”

katia Hay, Clinical trial coordinator, Adocia

“I accomplished a better understanding on the role of the PRRC. Very knowledgeable [speaker] with a good presentation style.”

Adrian Dunleavy, UK Quality & Regulatory Manager, Freudenberg Performance Materials LP

“Excellent. I was hoping to refresh, add to and update my knowledge. The webinar was excellent to remind me of areas that I had been involved with many years ago and add knowledge that is more relevant to my role now. I found the topics of the workshop particularly relevant.”

Mary-Ann Tite, Regulatory Manager, Pets |Choice

“It was well laid out and formatted especially for myself who does not have a regulatory role currently. I was hoping to achieve a firmer understanding and overview of submission within the EU, and believe I achieved this. [Speakers] were very knowledgable and provided great answers to all questions— supportive but challenged us when doing the workshop. I liked all areas of the course.”

Louise Dunn, Pharmacovigilance and Technical advisor, Zoetis

“Fantastic webinar! Speakers were very knowledgeable, clear, concise, and open to questions at any time—providing in depth background information were appropriate as well. The content was very interesting and I think a very good amount was covered considering the timescales. I enjoyed the workshop a lot. I thought it was a good way to try and put into practice what we had learnt during the webinars. I also thought a very good amount of information was covered for an introduction into the sections of the dossier.”

Emilija Stabingyte, Regulatory & Quality Coordinator, Zoetis UK Limited

“Great. I particularly liked the global information [section] and it was up to date information so I thought it was really complete.”

Maya El Fayoumi, Chargée Affaires Réglementaires, Panpharma Ltd

“The webinar is well constructed and the speaker is a very polite and prepared person. I managed to get the initial information needed to start studying and understanding the process validation program, the exercises [were] very helpful.”

Alessandra Fanzini, CDMO, REITHERA SRL

“I really enjoyed this webinar. I will be recommending it to colleagues as a great source of information and introduction to process validation. The material was engaging, and [speakers'] knowledge/experience was communicated very well. I greatly enjoyed the content and presentation style. Topics were split up and presented in a logical order and the exercises were very helpful to reiterate the information that was presented.”

Brianna Boehm, Process Validation Technical Writer, Aldevron