Dr. Ranbir is a seasoned professional with over 9 years of experience in clinical research and medical writing, specializing in the production of high-quality documents across diverse therapeutic areas. His expertise encompasses a wide range of regulatory documents, including clinical study reports (CSRs), clinical protocols, investigator brochures (IBs), CTD modules, informed consent forms (ICFs), safety narratives, FDA responses, development safety update reports (DSURs), orphan drug applications, briefing books, and more, with a strong emphasis on precision and quality assurance.

In addition to regulatory writing, Dr. Ranbir is adept in medical communications, having authored manuscripts, abstracts, slide decks, standard operating procedures (SOPs), research posters, summary reports, and lay summaries. He excels in ensuring data integrity, performing thorough literature reviews and maintaining the highest standards in quality checks.

At Zoe MedCare, Dr. Ranbir offers specialized medical writing services to biopharmaceutical companies and clinical research organizations (CROs) across Europe, the UK, and the US. Dr. Ranbir manages a team of skilled and dedicated medical writers and quality control reviewers. His collaborative approach, attention to detail, and commitment to continuous learning drive his success in delivering impactful solutions to cross-functional teams.