Our services

medical / publication 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 multidisciplinary clinical research 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 vast experience drawn from academia and the pharmaceutical, biotechnology and medical device industries. SOCAR Research’s medical writing services include clinical and regulatory writing in addition to scientific communications and educational materials.
Benefit from our vast experience in
scientific writing
drawn from academia and
the pharmaceutical, biotechnology and medical device industries.

Regulatory & 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


Preparation of conference materials (abstracts, poster presentations and slide sets)
Preparation, writing and submission of manuscripts for publication in major journals (e.g. NEJM, Lancet,...)
Preparation of responses to the editors / reviewer comments and follow-up until final correspondence received
Review of manuscript proofs prior to publication
Editorial (e.g. formatting, graphic) support
Preparation of educational materials for healthcare professionals and pharmaceutical industry personnel
Literature reviews
Publication planning and project management