In today's dynamic regulatory landscape, the importance of a robust Pharmacovigilance (PV) system cannot be overstated. Regulatory scrutiny is intensifying, underscoring the necessity for proactive PV measures. Organizations must adapt to evolving regulations and heightened inspection standards to safeguard public health.
Regulatory agencies mandate inspections to ensure Marketing Authorization Holders (MAHs) have the necessary infrastructure and personnel to fulfil PV obligations. These audits serve to identify and rectify non-compliance, mitigating risks to public safety.
Cliniminds-CRQA program is crafted to equip professionals with the essential skills for conducting and facing comprehensive PV audits and regulatory inspections. From strategizing your audit plan to delivering actionable insights, we provide a comprehensive understanding of PV auditing. This course caters to professionals across drug safety, regulatory, and quality assurance domains, including auditors new to the field.
Join us as we delve into crucial topics such as PV audit methodologies, processes, and documentation, emphasizing quality systems and regulatory compliance. Together, let's fortify the foundation of Pharmacovigilance, ensuring the safety and well-being of patients worldwide.
Program is offered by our Training Partner Cliniminds, a global leading in the life sciences sector education and training. CRQA Auditors would bring in the pharmacovigilance audits and inspections expertise to the program.
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