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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 7 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 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 53 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 13 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 70 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 23 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

“EXCELLENT - worth the time and money. I hoped to gain additional knowledge in Pharmacovigilance/show me areas where I may be lacking. I did not want the training to be a waste of time out of the office...[it was] definitely not — I would highly recommend
the speaker and the course. 5/5 overall.”

Nicky Höll, Pharmacovigilance Manager, Eurolab (Pty) Ltd

“Overall, 5* - Excellent. I learnt a lot of things in detail. Now happily I can implement those with my current job. All the sessions very helpful for me. Excellent speaker, explained very well and in detail for every question. ”

Vijaya Laxmi-Tunakala, QA Officer, Pharmacare Premium Ltd

“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 the course is well organized, contains relevant information and provides a good starting point for registration activities in the covered geographical area. I think if a person gets responsibility for regulation in EUEA, Russia, Ukraine, Kazakhstan and Belarus countries — this course is a great source of relevant information. ”

Elena Dolgodilina, Regulatory Affairs Manager, Geistlich

“The speaker was excellent and shared a lot of interesting information regarding national registration in the CIS region. All in all, it was good and useful webinar.”

Marina Baum, CMC specialist, JGL d.d.

“That was perfect, thank you! The presentation, content and presenter were very good. I hoped to get basic understanding of the FDA submission pathways and this is certainly achieved! Overall, I am very satisfied having followed the course.”

Elisabet Jamez, Biocompatibility Expert, Nelson Labs

“The training materials were well prepared and of high quality. These will be an excellent reference when we want to start planning device registrations for US market. Overall, very happy with the content, speaker and presented materials.”

Veerle Leijnen, Senior RA Executive Manager, Nikkiso Belgium

“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

“The Webinar gave me a lot of information around FDA [particularly] on general information/introduction to FDA Overall, [the speaker] was very good in explaining the topics and also in responding to the various questions. It was a useful webinar, and I would recommend it to others who aren't that familiar with the FDA/general legislation.”

Judith Handwerger, Manager Regulatory Affairs, Alfred E. Tiefenbacher (GmbH & Co. KG)

“The Webinar gave me a lot of information around FDA [particularly] on general information/introduction to FDA Overall, [the speaker] was very good in explaining the topics and also in responding to the various questions. It was a useful webinar, and I would recommend it to others who aren't that familiar with the FDA/general legislation.”

Judith Handwerger, Manager Regulatory Affairs, Alfred E. Tiefenbacher (GmbH & Co. KG)