Barbara Grossman
Barbara is a Biochemist and a Medical Writer, Editor and Teacher by profession, with 20+ years’ experience in the pharmaceutical industry. Barbara has started her own medical writing and consultancy business (Hawkeye Medical Limited) and built up and managed the medical writing group at Covance, the contract research organisation, working in a wide range of therapeutic areas. Since May 2019, Barbara is the EMWA’s President and is an Associate Editor of Medical Writing, EMWA’s journal.
Effective Technical Writing & Editing
11 Feb 2021
Expert advice on how to write and edit scientific and medical texts, technical documents and those documents needed for regulatory submission.
Medical Writing for Medical Devices
3-4 Mar 2021
How to produce quality regulatory documents including the clinical evaluation report (CER)
Successful Medical Writing
24-26 May 2021
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.
Effective Technical Writing & Editing
23 Sep 2021
Expert advice on how to write and edit scientific and medical texts, technical documents and those documents needed for regulatory submission.
Effective Technical Writing & Editing
24 Sep 2021
Expert advice on how to write and edit scientific and medical texts, technical documents and those documents needed for regulatory submission.
Successful Medical Writing
4-6 Oct 2021
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.
Successful Medical Writing
11-13 Oct 2021
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.
Medical Writing for Medical Devices
19-20 Oct 2021
How to produce quality regulatory documents including the clinical evaluation report (CER)
Medical Writing for Medical Devices
21-22 Oct 2021
How to produce quality regulatory documents including the clinical evaluation report (CER)