Pharmaceutical Regulatory Affairs
- Registration of foreign manufacturing plants and drugs including API, Medical Devices and Diagnostic kits.
- New drug approvals
- Dossier submissions.
- NOC for BA/BE services
- Clinical Trials Protocols approvals
- Marketing Strategies and approvals
- Safety Reporting
- Clinical Trials licensing
- Clinical Trial Approval for I-IV phases of Clinical Researches
- Obtaining import licenses and permits for commercial and experimental use
