Medical Writing

Medical Writing is a vital part of clinical research, it is essential and ever more important activity required at every stage of developing a therapeutic product. Writers works along with the Clinical Data Management, Biostatistics, Pharmacovigilance and Project Management teams to deliver Precise, Well-Timed, credible, complete and Cost effective documents to the main ethical and scientific standards.

Medical Writing is a vital part of clinical research, essential and ever more important activity required at every stage of developing a therapeutic product. Writers works along with the Clinical Data Management, Biostatistics, Pharmacovigilance and Project Management teams to prepare Research-Related documents, Regulatory Documents, Disease Or Drug-Related educational literature, Publication articles and journal in Precise, Well-Timed, credible, complete and Cost effective documents to the main ethical and scientific standards.

To conduct a new clinical studies or for registering new products, many essential documents are required to be submitted to international regulatory agencies such as the US FDA, EMEA, DCGI etc, and these documents will be prepared by medical writers.

Popular Designations

• Safety Writing Expert (ICSR, PSUR etc.)
• Medical Writer I (CFR, ICF, Protocol, CRS etc.)
• Medical Writer II (CFR, IFR, Protocol, CSR etc.)
• Medical Communication Specialist
• Proofing ,Editing experts
• Translator