Pharmacovigilance

Established Pharmacovigilance system in place to continuously monitor the adverse Events/other safety issues of a Drug and thus promote safer use of medicines.

• Serve as the point of contact for the local Health Authority or liaise with the contractual partners

• Reporting and maintaining Adverse events (spontaneous and solicited cases) from the country to the contractual partners.

• Conducting reconciliation of adverse events reports with contractual partners, as applicable

• Archival of all safety-related documents.

• Prepare for audits/inspections for their contractual partners

• Identify and communicate potential safety issues

• Deliver training to all employees of the company

• Complete and document required PV training within required timelines

At ATE, we believe in patient’s safety, kindly contact us for any of your queries/Notification with regards to Pharmacovigilance/Adverse Drug Safety Reports (PV/ADR) for any kind of adverse drug reactions or events, safety & efficacy etc. or any Product Quality Complaints of Pharmaceuticals & other products to the below mentioned contact details:

• Phone Number: 17213443, 17213332

• Fax: 17213121

• Email: quality.pv@alhamert.com

QMS