Medical and Scientific Writing
Medical and Scientific Writing done as part of a clinical trial or as a stand-alone project, the professional medical writers at Mediclin Clinical Research combine medicine, science, and technical writing to deliver concise documents for all stages of regulatory, project management, and final reports.
With the unique blend of medical writers comprising of doctors, pharmacists, scientists and grammar experts, Mediclincr provides medical writing services from essential documents such as study synopsis and protocol, clinical study report (CSR), investigator’s brochure (IB) informed consent form (ICF), case report form (CRF), etc. ProRelix has a devoted team of subject experts for abstract writing, manuscript writing, journal articles, and submissions. We provide these Medical and Scientific Writing and publication services in India, USA, Europe, UK
Clinical Research
Writing
- Study Synopsis & Protocol
- Clinical Study Report (CSR)
- Investigator’s Brochure (IB)
- Informed Consent Form (ICF)
- Case Report Form (CRF)
- Quick Design And Layout
- Direction High Level Idea
- And Concept Illustration
Regulatory & Pharmacovigilance
- Clinical sections of common technical documents (CTDs) & new drug applications (NDAs)
- Risk Management Plans (RMP)
- Periodic safety update report (PSUR)
- Benefit risk evaluation report
- Patient safety summaries/ narratives
- Summary product characteristics (SPC)
- Package Inserts
Publication
- Abstracts writing
- Manuscript writing
- Journal articles & submission