Lead, author and finalize aggregate reports, including but not limited to PBRERs/PSUR, DSURs, PADERs, RMPs, ACOs, and line listings author responses to regulatory agency/ Pharmacovigilance Risk Ass ... view more

• Signal
• RMP
• Compliance
• Aggregate reports
• Pharmacovigilance

Major activities of work Profile: - CAPA closure verification Audit of manufacturing Sites (Including sites). Tracking CAPA closure and sustenance. Candidate may have to participate in the supportin ... view more

• Quality Management
• Quality Assurance

We are looking for candidates for Project Manager position to help conducting Clinical trials at Dellhi, Mumbai & Kolkata CRO sites. Candidates who can join with immediate effect will be given p ... view more

• Drug Regulatory Affairs
• ICH-GCPC
• linical Research
• Regulatory Affairs
• Medical Writing
• Drug Safety
• Clinical Operations
• Pharmacology
• Pharma
• covigilance
• Clinical Trials
• CDSCO

Designation Offered : Head Customer Service, Logistics & Supply Chain Business Line : Health Care Location : Andheri, Mumbai Organization : Evonik India Pvt. Ltd.   ... view more

• Supply Chain Management
• Warehouse Management
• Logistics

Manager - Regulatory Affairs & Patient Safety   Do you have expertise in, and passion for Regulatory Affairs? Would you like to apply your expertise in a company that follows the science a ... view more

• Regulatory Affairs
• Patient Safety
• Import registration
• Pharmacovigilance
• CDSCO
• DCGI
• India Regulatory markets

New Drug Approvals and Regulatory support for new product launches, BE NOC for export "• Timely submission and approval of the products for new drug applications including clinical trials ... view more

• import & registration
• NPPA approvals
• Technical Discussions
• New Product
• Due Diligence
• Clinical Trials
• Supply Chain
• Follow Ups
• CDSCO
• Drugs and Cosmetics Acts
• Rules of India for new drug approval