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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:

  • 26-27 Jun 2025 Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products
  • 9-11 Jul 2025 Biotechnology for the Non-Biotechnologist

See all 7 courses

Clinical Research

Next events:

  • 23-24 Jun 2025 Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3
  • 7 Jul 2025 GCP and Clinical Research Update - Hot Inspection Topics

See all 20 courses

GxP

Next events:

  • 24-25 Jun 2025 Development of Combination Products: Critical Interactions
  • 26-27 Jun 2025 Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products

See all 28 courses

Medical Technology

Next events:

  • 19-20 Jun 2025 Metered Dose Inhaler (MDI) Technology
  • 3 Jul 2025 Smart Packaging and Electronic Patient Information

See all 12 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:

  • 18-19 Jun 2025 Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application
  • 23-24 Jun 2025 Pharmaceutical Regulatory Affairs in the Middle East

See all 55 courses

Vigilance

Next events:

  • 16-17 Jun 2025 Understanding Pharmacovigilance Regulations in APAC
  • 1 Jul 2025 Pharmacovigilance Aspects of Licensing Agreements

See all 18 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...

“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

“My goal was to gain a deeper awareness and understanding of what is required in the different sections of a dossier for submission in the EU. I think the course definitely accomplished this and there was lots of useful information, which was very well explained. I can confidently say that I left knowing a lot more than I initially thought I would.”

Emilija Stabingyte, Regulatory & Quality Coordinator, Zoetis UK Limited

“Very competent.”

Jesper Bergwik, Regulatory Affairs Associate, Bioglan AB

“Loved it. Great content, great presenter/instructor. He was engaging and explained things clearly, answering questions along the way. I particularly liked the way he brought the content to life and gave greater insight through sharing examples of his personal experiences. Great course, would recommend.”

Kishori Amatya, PV and MI officer, Jenson R+

“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

“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

“An excellent webinar, delivered by a very knowledgeable person in an impactful way by great use of analogies and first hand experiences that brought the learning to life. First experience and a very pleasant one.”

Lee Gittings, Country Manager, Biofrontera UK Ltd