- Pharmacovigilance System Master File (PSMF)
- Risk Management Plan (RMP)
- Periodic Safety Update Report (PSUR)
- Adverse Drug Reaction Monitoring (ADRM)
- Customised Scientific Manuscript Writing
- Individual Case Safety Report Processing
Drug development takes billions of dollars to go through different stages till the safety is determined. It then requires to have a systematic process to establish the safe and sound reach of the drug for the humanity. A proper manufacturing process & efficient storage is required as per the norms set in. In spite of the huge expenses incurred in the development & launch phases the companies are worried about the regulatory rules & regulations which are subject to change from time to time. This further has cost the companies huge punitive amounts to clear the processes.