Téléphone : +33 - 7.67.97.61.11
Courriel : devendra.medcoms@gmail.com
Why
Choose
Me
18+ years of experience across regulatory writing, clinical documentation, and medical communications
deep industry knowledge and hands-on expertise.
Proven Expertise
Worked with top pharma and CROs including Takeda (via ICON), Sanofi (via Aixial), AB Science, Jubilant Clinsys, GVK Biosciences, and Pfizer (via GENPACT).
Global Experience
From clinical trial protocols, CSRs, safety narratives, and CTDs to training decks, medico-marketing materials, and scientific publications – deliver end-to-end medical writing solutions.
Comprehensive
Skill Set
Expertise across diverse areas including oncology, neurology, cardiology, vaccines, rare diseases, women’s health, infectious diseases, and immunology.
Therapeutic Breadth
Strong foundation in ICH, EMA, FDA, and global regulatory standards, ensuring documents meet the highest scientific and compliance benchmarks.
Quality
& Compliance
Known for adaptability, clear communication, and delivering accurate, compliant, and impactful documents on time.
Client-Centric Approach