FORUM INSTITUT
FORUM · Institut für Management GmbH
Vangerowstraße 18
69115 Heidelberg
Email: service@forum-institut.de
Phone: +49 6221 500-500
Fax: +49 6221 500-505
Course: Scientific Wirting in Regulatory Affairs
Scientific Writing
and Reviewing in
Regulatory Affairs
2018-12-09 2019-04-10 relexa hotel Lurgiallee 2 60439 Frankfurt Frankfurt-Main@relexa-hotel.de +49 69 95778-0 +49 69 95778-876

Scientific Writing and Reviewing in Regulatory Affairs

Update your English writing skills - with many practical exercises

After completing this seminar, participants will be aware of the key regulatory requirements when preparing texts, with a greater awareness of the importance of proper English writing, reviewing and proofreading processes.
Topics
  • Free writing versus regulatory restrictions
  • Writing and reviewing regulatory documents
  • Editing and proofreading documents
  • Package leaflet - regulatory linguistic restrictions and user-friendly writing
  • Good writing skills - example: clinical overviews and summaries

This distinguishes our event

100%
Overall impression: 100 % of the participants' feedback was very good or good (April 2018)
100%
Course content: 100 % of the participants' feedback was very good or good (April 2018)
89%
Practical benefit: 89 % of the participants' feedback was very good or good (April 2018)

Aims and objectives

After completing this seminar, participants will be aware of the key regulatory requirements when preparing texts, with a greater awareness of the importance of proper English writing, reviewing and proofreading processes.
Practical examples regarding the English wording in package leaflets and clinical overviews and summaries complete this seminar.
Who should attend
This seminar is intended for all those working in regulatory departments in the human and veterinary pharmaceutical and medical device industries with basic experience in writing, reviewing or proofreading regulatory documents in English.
Participants should have good English reading and writing skills and a basic knowledge of regulatory documentation.
This seminar is restricted to 15 participants.
Your speakers
Beate Beime
Beate Beime Pharma Consulting, Oldenburg, GERMANY

Barbara Grossman
Hawkeye Medical Limited Medical Writing & Consultancy, GREAT BRITAIN


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Pharma Webcast Global RA & PV

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We would like to invite you to join our live webcasts, where local regulatory affairs and vigilance experts will inform you every two months of the latest news and trends in global marketing authorisation and drug safety.

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More on our quality criteria

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IMI (Innovative Medicines Initiative) defined quality criteria for professional training and education. We follow these criteria and, as a signatory, we are an active partner in further developing and optimising the quality standards.

An aggregate evaluation of participants' feedback on all FORUM's healthcare training courses (evaluation period from 10.2017 - 09.2018 produced a result of 1.6 (based on a school grading system of 1-6).

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