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Pharmacovigilance & Drug Safety Services Pharmacovigilance has become a critical phase in the Clinical Development Programs of pharmaceutical companies. The regulations on safety monitoring have become
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Pharmacovigilance and drug safety involves the monitoring, detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems.
Marketing authorization holders, manufacturers, and sponsors of pharmaceutical products are required to file pharmacovigilance and drug safety reports.
Pharmacovigilance and drug safety reports can be filled out electronically through specific reporting systems provided by regulatory authorities.
The purpose of pharmacovigilance and drug safety is to ensure the safety and efficacy of pharmaceutical products by identifying, assessing, and minimizing risks associated with their use.
Information such as adverse drug reactions, medication errors, lack of efficacy, and other drug-related problems must be reported on pharmacovigilance and drug safety reports.
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