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In-house & bespoke training:
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

Sample course outlines include:

  • Biosimilars
  • Biotechnology for the Non-Biotechnologist

See all 6 course outlines

Sample course outlines include:

  • Risk Management for Clinical Research
  • Advanced Project Management in Clinical Research

See all 24 course outlines

GxP

Sample course outlines include:

  • A Practical Introduction to Good Clinical Practice (GCP)
  • An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices

See all 35 course outlines

Sample course outlines include:

  • An Introduction to the Design and Development of Medical Devices
  • An Introduction to the ‘Soft Side’ of Technology Transfers

See all 20 course outlines

Sample course outlines include:

  • Effective Technical Writing & Editing
  • Medical Editing for Peer-Reviewed Journals

See all 6 course outlines

Sample course outlines include:

  • A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products
  • A Practical Approach to Veterinary Vaccine Development and Registration in the EU

See all 67 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 20 course outlines

5*. I really enjoyed and learned from this course and would recommended to others .

Derek Farrell, Quality Technician, Fire1 Foundry

The speakers were excellent! The content and presentation were satisfactory as well. I accomplished what I was hoping to achieve.

Marija Apostolova, Submission Coordinator - CIS region, ALKALOID AD Skopje

I wanted to get a good overview of biotechnology: history, development, science, processes, regulations and future and this goal was 100% fulfilled.

All lecturers were highly competent in terms of content and style of presentation.

Andy Bossert, CQV Engineer, Lonza

All of the speakers were very knowledgeable, well prepared and presented the topics in a structured and comprehensible manner. A session I thought would be rather arid turned out to be entertaining and instructive at the same time. The seminar gave a very complete overview of the topics.

Max Hofferberth, DSTL, Hoffmann LaRoche


Susann Bandholtz-Irgang, , Vetter Pharma-Fertigung GmbH & Co

Very good. Recommend.

Agnieszka Mickiewicz, R&D Manager, Teva Pharmaceuticals

The content of this webinar was clear and consistent. I liked the fact that there was interaction and the concepts were able to be practiced.

Andreea Elena Stoica, Analytical Researcher, Sindan SRL

Valuable Webinar and very good interactions with the speakers.

Celine Aubertin, International Regulatory Affairs Manager, NOOUS FINANCE AU NOM ET POUR LE COMPTE DE PIERRE FABRE SA

[Speaker] answered all the questions, and the discussions were super helpful. Very satisfied. Would recommend.

Camila Tavares, International Medical Manager, Novo Nordisk

The process was well thought out. I would recommend.

Furkan Akbulut, Project Leader Regulatory Affairs, Bentley InnoMed GmbH