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].