Management Forum courses now available at IPI Academy - visit IPI for an updated experience and a broader selection of courses and subjects

In-house & bespoke training:
Medical writing

The process for new drug approvals relies heavily on the quality of documentation submitted to the regulatory authorities, and a high standard of medical writing plays a vital role in ensuring a positive outcome. Our medical writing training courses will provide delegates with all the tools and techniques necessary to comply with the required standard.

 

Effective Technical Writing & Editing

In-house & bespoke training

Expert advice on how to write and edit scientific and medical texts, technical documents and those documents needed for regulatory submission.

Rated by attendees to the public programme

Typically presented by Barbara Grossman (bio)

Typical duration: 1 day
Pricing from £450 per attendee
Delivery: collaborative classroom

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Medical Writing for Medical Devices

In-house & bespoke training

How to produce quality regulatory documents including the clinical evaluation report (CER)

Rated by attendees to the public programme

Typically presented by Janette Benaddi (bio) , Barbara Grossman (bio)

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

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Successful Medical Writing

In-house & bespoke training

Success in the pharmaceutical industry depends on the speed and efficiency of new drug approvals and the quality of documentation submitted to the regulatory authorities. This intensive, practical medical writing course will benefit participants by enabling them to achieve this standard.

Rated by attendees to the public programme

Typically presented by Barry Drees (bio) , Barbara Grossman (bio) , James Visanji (bio)

Typical duration: 3 days
Pricing from £1,200 per attendee
Delivery: collaborative classroom

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I got what I hoped for - i.e. an introduction to the types of documents I will come across, how to select the right content, and how to write it. On top of this, it was extremely useful for me to receive all the little tips and tricks. I think all presenters were very generous in sharing their experience. This includes how to manage difficult stakeholders, when to stick to guidelines and when to use common sense, where to find links on correct use of English, and even be able to ask questions in the future on how to present data.

Lone Helboe, ,

I really enjoyed it! The webinar was well structured, the contents well chosen and Barbara and Janette managed to bring ("teach") their respective contents to us in a simple and effective manner.

Lena Jung, Clinical Affairs Manager, Richard Wolf GmbH

It is very difficult to make training engaging when performing it remotely but I felt this webinar was really successful from the assistance from Management Forum, to the course content and the interesting speakers. The attendees were really good too as they made the most of the opportunities to participate and ask questions. Overall, I really enjoyed it. Thank you.

Jennine Walker, Clinical Affairs Manager, Dermal Laboratories Ltd

The content was really good. A lot was covered. Very experienced presenters, and very knowledgeable.

Isabelle SABOUNTCHI, Senior Consultant, Medical Devices, Beyond Conception GmbH

An enjoyable and interesting course with good participant interaction. I believe I am now better equipped to prepare quality documentation with improved accuracy and readability.

Jessica Fischer, Safety Medical Writer, Ferring Pharmaceuticals

I wanted to get some hints and tips on general improvements in writing style when compiling regulatory dossiers - and interested to know more about the required content in the clinical section of the eCTD, which I believe was delivered.

Judith Rowland, Senior Regulatory Affairs Manager, Nerudia Limited

Good, engaging and knowledgeable speakers.

Marit Sorum, Regulatory Affairs Manager, Pharmaq

I was really satisfied with the webinar. It reflected my expectations and it addressed my needs.

Roberta Grimaldi, Clinical research principal scientist, GSK

The webinar was highly informative and I would recommend it to a colleague.

Pascal Häfliger, R&D Scientist, Innomedica

I enjoyed the course and learnt more tips on preparing better quality documentation.

Louisa Dew, Regulatory Affairs Consultant, NDA Regulatory Science Ltd