Medical writing services for clinical trials

Documenting your research plans and results may require medical writing that is flexible in scope. APCRA’s Medical Writers not only have a wide breadth of knowledge, but also extensive experience drawn from the pharmaceutical industry, clinical research organisations and academia and can deliver accurate, timely and cost effective documents to the highest ethical and scientific standards.


APCRA provides regulatory Medical Writing and Scientific Writing services, as well a range of language support services, such as translation of clinical research documentation into Chinese and other Asian languages. Such services are designed to support pharmaceutical, biotech and medical device companies’ work with academic and other clinical research organisations within the APAC region.

 

Academic Editing

 

Provide expert assistance in getting papers published in academic journals by offering academic English editing. Papers in clinical sciences, biotechnology, molecular biology, biochemistry, and other allied fields.


Regulatory Medical Writing

 

  • Study protocols
  • Clinical study reports
  • Investigator brochures
  • Patient safety narratives
  • Informed consent documentation
  • Patient brochures
  • Pharmacovigilance documents
  • Standard Operating Procedures

 

Scientific Writing

 

  • Manuscripts
  • Scientific abstracts
  • PowerPoint slides and presentations

 

Acadmeic Translations

Translation of scientific papers, clinical research documents and clinical trial legal documents from English to Chinese and Chinese to English.