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Life Sciences

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

Biopharma

Sample course outlines include:

Biosimilars
Biotechnology for the Non-Biotechnologist

See all 6 course outlines

Clinical Research

Sample course outlines include:

Advanced Project Management in Clinical Research
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects

See all 25 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 52 course outlines

Medical Technology

Sample course outlines include:

An Introduction to the Design and Development of Medical Devices
Be In the Know With Pharma 4.0: Building The Business Case For Pharma 4.0

See all 20 course outlines

Medical Writing

Sample course outlines include:

Breaking the Code – Achieving Publication Success in Scientific Journals: Dealing with Reviewers' Comments and Resubmission
Breaking the Code – Achieving Publication Success in Scientific Journals: Journal Submission and Publication

See all 11 course outlines

Regulatory Affairs

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 68 course outlines

Vigilance

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

Training options

All of our course outlines are available:
	Ready made for any number of participants	or		With a programme and presenters customised to your requirements
And in your preferred format, or combination:
	Face-to-face training at your location	or		Webinar/interactive online

“Overall, this is a good seminar. It is a little long, but that is to be expected looking at the contents and countries to be covered. 5* - I would recommend.”

Kong Kong Weng-Yip, Assistant Manager RA, DUOPHARMA (M) SENDIRIAN BERHAD

“Overall, it was a wonderful webinar and has helped me further expand my knowledge on the EU/UK regulations. I look forward to participating in future webinars.”

Iva Martinovic, Medical Information Professional, Teva

“My expectation was to gain as much knowledge as possible about EAEU regulations. It was very helpful and useful to get EAEU region overview and understand regulatory approach in each country.”

Maryna Orudzheva, Regulatory Manager CIS, Accord Healthcare Polska Sp. z o.o.

“The presentation was outstanding. The presenters were welcoming. The session was interactive and insightful.”

Vivian Ilonzeh, Director Reg Operations, Bristol Myer Squibb

“This was an excellent webinar. Very useful and [speaker] has a lot of knowledge and experience, giving us examples from real life, making the concepts easier to understand and the course more enjoyable, was fantastic - kept me engaged the entire time. Very well organized.”

Maria Jesus Lopez Villanueva, QA Administrator Eng, Endomag

“Very good seminar which covered all important points around the production and maintenance of the PSMF. The speaker was excellent with a profound knowledge of the topic.”

Marie-Christine Klös, Global PV Specialist, Boehringer Ingelheim Vetmedica GmbH

“Very Good. I wanted to get an overview of EU Pharmaceutical Regulations and to understand regulatory strategies to bring new products quickly into the market. The course covered everything I needed and even more. ”

Chitra Saxena, Senior Manager Regulatory Affairs, Lupin Healthcare (UK) Limited

“It was very useful to have specific ideas, tools, websites and portals introduced as to what should be done for CRO oversight.”

Kenji Tada, Unit Manager, Clinical Operation Unit, JCR Pharmaceuticals Co

“Very good. [Speaker was] very experienced.”

Celine Anselmetti Dayer, Director, Regulatory Affairs, Debiopharm Research & Manufacturing SA

“Very good.”

Peter Wæde Hansen, Senior International Medical Manager, Novo Nordisk AS