Regulatory expert

Summary To write review and manage the production of high quality clinical and safety documentation for submission to regulatory authorities in support of marketing applications To provide authoritative documentation-related consultancy to other line functions To coach mentor and train less experienced writers Major accountabilities To author ...

Role Overview: As a Medical Writer at Novartis Healthcare Private Limited, you will be responsible for writing, reviewing, and managing the production of high-quality clinical and safety documentation for submission to regulatory authorities in support of marketing applications. Your role will also involve providing authoritative documentation-related...

**Summary**: **About the Role**: **Major accountabilities**: - To author, review and/or independently manage high quality clinical and safety documents: complex Clinical Study Reports (CSR), Risk Management Plans (RMP), complex CTD submission documents (clinical overviews, summaries of clinical efficacy and safety, summaries of clinical pharmacology and...

Position – Regulatory ConsultantCompany InformationWe are a reputed Pharmaceutical Consulting firm working in the area of GMP and Global Regulatory Affairs. We have our head office in Mumbai and subsidiaries in Singapore, Malaysia, Australia and in Europe. We have been providing high quality & timely consulting service to the Pharmaceutical Industry in...

Position – Regulatory ConsultantCompany InformationWe are a reputed Pharmaceutical Consulting firm working in the area of GMP and Global Regulatory Affairs. We have our head office in Mumbai and subsidiaries in Singapore, Malaysia, Australia and in Europe. We have been providing high quality & timely consulting service to the Pharmaceutical Industry in...

Position – Regulatory ConsultantCompany InformationWe are a reputed Pharmaceutical Consulting firm working in the area of GMP and Global Regulatory Affairs. We have our head office in Mumbai and subsidiaries in Singapore, Malaysia, Australia and in Europe. We have been providing high quality & timely consulting service to the Pharmaceutical Industry in...

Position – Regulatory Consultant Company Information We are a reputed Pharmaceutical Consulting firm working in the area of GMP and Global Regulatory Affairs. We have our head office in Mumbai and subsidiaries in Singapore, Malaysia, Australia and in Europe. We have been providing high quality & timely consulting service to the Pharmaceutical...

Position – Regulatory ConsultantCompany InformationWe are a reputed Pharmaceutical Consulting firm working in the area of GMP and Global Regulatory Affairs. We have our head office in Mumbai and subsidiaries in Singapore, Malaysia, Australia and in Europe. We have been providing high quality & timely consulting service to the Pharmaceutical Industry in...

Position – Regulatory ConsultantCompany InformationWe are a reputed Pharmaceutical Consulting firm working in the area of GMP and Global Regulatory Affairs. We have our head office in Mumbai and subsidiaries in Singapore, Malaysia, Australia and in Europe. We have been providing high quality & timely consulting service to the Pharmaceutical Industry in...

Position – Regulatory ConsultantCompany InformationWe are a reputed Pharmaceutical Consulting firm working in the area of GMP and Global Regulatory Affairs. We have our head office in Mumbai and subsidiaries in Singapore, Malaysia, Australia and in Europe. We have been providing high quality & timely consulting service to the Pharmaceutical Industry in...