Minimum
₹900,000 Per Year
Maximum
₹1,300,000 Per Year
- Monitor and evaluate adverse drug reactions and safety reports. - Conduct risk assessments and prepare safety reports. - Collaborate with regulatory agencies and ensure compliance. - Review and analyze safety data from clinical trials and post -marketing sources. - Develop and implement pharmacovigilance procedures and protocols. - Provide training on safety reporting and risk management. - Prepare regulatory submissions and safety documentation. - Monitor and track safety signals and trends. - Participate in safety meetings and reviews. - Ensure timely and accurate reporting of adverse events.
