Medical Writing

Medical writing is an integral part of clinical research where a precise, accurate and timely presentation of your scientific ideas and study results is vital. Our medical writers collaborate closely with the clinical research multidisciplinary team to achieve this.

We understand the standards and expectations of journal editors and regulatory authorities. We apply our scientific writing and editing experiences to your documents. Our medical writers have a vast experience drawn from academia, pharmaceutical, biotechnology and medical device industry.

SOCAR Research's medical writing services include clinical and regulatory writing in addition to scientific communications and educational materials.

Examples include:

Regulatory and Clinical writing

ICH compliant Clinical Study Reports (CSRs) for Phase I to IV studies including CSR Synopses for public disclosure
Study Protocols (ICH compliant)
Clinical and non clinical sections of the Common Technical Document (CTD) including summaries and overviews for EU or US Regulatory Authorities
Investigator Brochures
Patient safety narratives
Patient information sheets and Informed Consent forms
Pharmacovigilance documents such as Periodic Safety Update Reports, Development Safety Update Reports

Scientific Communications

Conference materials (abstracts, poster presentations and slide sets)
Manuscripts for publication in major journals (NEJM, Lancet, Circulation..)
Journal/conference submission and follow-up until published
Editorial support
Educational material for healthcare professionals and pharmaceutical industry personnel
Literature reviews
Publication planning

Medical writing and communication
Contact Careers Privacy Policy Terms of Use Site Map  e-SOCDAT™ 
© 2014 SOCAR Research SA. All rights reserved. Website developed by SOCAR Research SA.