Ongoing safety surveillance of approved drugs to ensure continued compliance and patient safety.

Implementation and maintenance of pharmacovigilance systems to support safety reporting and compliance.

Qualified and Local Pharmacovigilance Personnel to ensure regulatory compliance in different regions.

Handling and reporting adverse event cases efficiently and in compliance with regulatory standards.

Systematic monitoring of scientific literature for safety signals and regulatory reporting.

Detecting, assessing, and responding to potential drug safety concerns.

Preparing and submitting safety reports to regulators as required.

Supporting global regulatory submissions for new and existing products.

Keeping clients informed on evolving regulatory requirements and industry best practices.