Our latest COVID-19 information - full Autumn programme of webinars now in place

Training courses & Webinars:
Medical writing

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. Our medical writing training courses will give you all the necessary practical guidance to ensure that you achieve the required standard in order for a positive outcome.

 

Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Training Course

Clinical Evaluation of Medical Devices: The Clinical Evaluation Report

1-2 Dec 2020 - Online webinar
Also on: 3 Dec 2020

Cover all the aspects of clinical evaluation in line with the European medical device regulations and applicable guidance documents

Presented by Janette Benaddi (bio)

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Effective Technical Writing & Editing Training Course

Effective Technical Writing & Editing

24 Sep 2020 - Online webinar
Also on: 11 Feb 2021

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

Presented by Barbara Grossman (bio)

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Medical Writing for Medical Devices Training Course

Medical Writing for Medical Devices

1-2 Mar 2021 - London
Also on: 3 Mar 2021

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

Presented by Janette Benaddi (bio)
Barbara Grossman (bio)

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I was hoping to get a better insight into writing reports and I would say that I definitely believe this was accomplished.

Neil McCann, Radiation Safety Officer, Elekta Limited

Barbara was technically brilliant and presented in a fun, challenging and friendly way. The content through the day was very useful, with good pointers and tips to improve the layout and quality of documents. The course structure and content was excellent, a good amount for a day's course. The presentation was fantastic and easy to follow with good exercises and interaction between presenter and course participants. Barbara has a deep knowledge of the subject matter which is delivered in an exciting way.

Nathan Entwistle, Senior Electronics Technician, Team Consulting

Very good course with plenty of personal interaction. The experience of the speaker gives added value as she can provide many examples and tips and tricks for reviewing a text.

Anke De Muylder, Quality engineer QA, Plasma Industries Belgium

Wonderful speaker, friendly and approachable. He manages to put a lot of information over in a short period, in a simple way, making it a lot easier to digest. Overall, an amazing teacher and incredibly knowledgeable in regulations concerning medical devices. I particularly liked the interaction and encouragement of the group activities and communication. An amazing course, well structured, and a knowledgeable, friendly and approachable speaker.

Hannah Vince-Drew, Clinical Research Associate, Bedfont Scientific

Janette is excellent. Her knowledge and ability to clearly communicate in an engaging way about the topic at hand really mean that it's very easy to learn and understand what is being discussed. The workshops were very useful in cementing what you've learnt and also bouncing ideas around. Absolutely excellent, fantastic speaker, wealth of knowledge, discussion welcomed!

Alex Hyde, Senior Regulatory Affairs Specialist , Sinclair Pharma

Eveything perfect!

Katarzyna Paluszynska, Clinical Associate, EduBroker Sp.zo.o

Janette was both very proficient regarding CE both also a lively and engaging presenter. It was a very good course, both content and duration was great

Per Videbæk, Team Manager Clinical Audiology, Demant a/s

Overall the course content was very good. Presentation was also good and very clear. The speaker was excellent and very active during the training.

Ildephonse Ngabonziza, Clinical Safety Manager, Genae Associates NV

The content is quite comprehensive, the presentation is clear and the speaker is very experienced. Both newbies and experienced people can benefit from this course, especially at the time of MDR transition.

Huajie Bu, Clinical Evaluations Manager, MED-EL Elektromedizinische Geräte GmbH

The speaker was very knowledgeable, able to answer all questions and allowed time for discussion of everyone's experiences. I learnt a lot and feel it was definitely worth the time.

Alice Sugden, Clinical Trials Submissions, AbbVie