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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 56 course outlines

Medical Technology

Sample course outlines include:

An Introduction to the Design and Development of Medical Devices
Building The Business Case For Pharma 4.0

See all 20 course outlines

Medical Writing

Sample course outlines include:

Achieving Publication Success in Scientific Journals
Dealing With Scientific Journal Reviewers: From Comments to Resubmission

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 72 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

“ I particularly liked working groups. Very good!”

Manon Schönholzer, Drug Safety officer, CIS Bio international

“Very good. I was expected to improve my knowledge and get some tips and I did it.”

Manon Schönholzer, Drug Safety officer, CIS Bio international

“Good presenter. ”

Hanne Storgaard, Clinical Quality Operations Lead- Suppliers, MSD Denmark

“The overall content was strong and informative and I believe there was a good mix of discussions, workshops and information. I wanted to deepen my understanding of clinical trial monitoring, particularly the common pitfalls and how to manage them effectively and how to best monitor online/off-site. I believe I’ve learned several valuable methods for identifying and evaluating issues when something goes wrong in a clinical study. I found the sections on risk-based monitoring approaches very insightful and applicable to my work. I also gained insights into ensuring patient safety and maintaining data integrity, as well as the principles of risk-based monitoring. The session on root cause analysis was especially valuable, and I plan to implement this approach in my own clinical study. Overall, I feel that I’ve achieved the goals I set out for this course.”

Isabella Åström, Clinical Research Associate, Atos Medical

“Overall very good.”

William Hensler, Principal, Alantra BioPharma

“Group tasks were good, as the interactive parts put theory into practice. Language, speed, flow, and overall presentation was good and easy to follow. Absolutely worth while as an intro to writing of SOPs.”

Thomas Bidstrup, Clinical Research Specialist, Ambu A/S

“The programme was well-structured and informative. The session provided practical guidance on structuring SOPs, using clear and concise language, and tailoring content to the intended audience. The real-world examples and actionable tips were especially valuable, and I now feel more confident in my ability to revise or create SOPs that align with current standards and expectations. The speaker was very knowledgeable and engaging throughout. Her expertise in SOP writing was clear, and she communicated complex ideas in a straightforward and easy-to-understand way. I particularly appreciated the practical examples and real-life scenarios shared, which made the content more relatable and actionable. She also encouraged questions and interaction, creating a welcoming and supportive learning atmosphere. Overall, her delivery significantly enhanced the quality and value of the training. It struck a good balance between theory and actionable advice, which made it easy to understand and apply.

In summary, the webinar was a valuable learning experience that provided useful tools and insights for writing effective SOPs.”

Amalia Neophytou, Trainer Analyst, Remedica Ltd

“I hoped to achieve a full picture of APIs for my new job and yes I accomplished it. A lot of information..
”

Marie Lucchini, Regulatory affairs Supervisor, Actylis

“I have accomplished a better understanding of API's after the two day webinar. Very good webinar which covers a good range of content, a little dense, so will need to refer back to it at some stage. Speakers were nice and accommodating. They clearly have a good understanding of the content they are presenting.”

Stephany Banglayan, Research and Development Analyst, Xeolas Pharmaceuticals

“I hoped to achieve a full picture of APIs for my new job and yes I accomplished it. A lot of information..
”

Marie Lucchini, Regulatory affairs Supervisor, Actylis