Medip Academy offers medical writing services for pharmaceutical companies, medical practitioners, students, researchers, NGOs and contract research organisations. Our Medical Writers have a wide breadth of knowledge and experience drawn from the pharmaceutical industry, clinical research organizations, and academia.

Examples include:

  • Conference materials (abstracts, poster presentations and slide sets)
  • Slide sets for healthcare professionals, CMEs and pharmaceutical industry
  • Product Monographs, Newsletters, LBLs
  • Training modules for pharmaceutical industry
  • Q & A Booklets
  • Manuscript writing
  • Journal/conference submission
  • Product website content (for both scientific and patient audiences)
  • Educational material for patients, healthcare professionals and pharmaceutical industry personnel
  • Medical marketing reviews and reports
  • Literature reviews
  • ICH GCP compliant Clinical Study Reports (CSRs); Phases I to IV, including CSR Synopses for public disclosure
  • Study Protocols
  • 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 Diaries
  • Clinical Trial Registry Synopses
  • Patient information including Informed Consent and Patient Brochures
  • Pharmacovigilance documents such as Periodic Safety Update Reports
  • Standard Operating Procedures (SOPs) covering all aspects of drug development including the design, conduct and reporting of clinical trials and the outsourcing of Sponsor responsibilities to a Contract Research Organisation (CRO)

If you have any more queries, or wish to know about our pricing structure and processes, please send us an email at [email protected].