Pharmacovigilance is more than adverse event reporting.

A strong Pharmacovigilance system goes far beyond collecting and reporting adverse events. It also includes risk management, signal detection, literature monitoring, regulatory compliance, audits, inspections, and continuous benefit-risk evaluation, all with one goal: protecting patient safety throughout the entire lifecycle of a medicinal product.

As regulatory requirements continue to evolve, maintaining a compliant Pharmacovigilance system is becoming increasingly complex.

At Interdos, we support Marketing Authorisation Holders with tailored Pharmacovigilance services, including Individual Case Safety Report processing, Qualified Person for Pharmacovigilance services, audits, inspection support, regulatory compliance and the implementation and maintenance of compliant Pharmacovigilance systems.

Because Pharmacovigilance isn't just about reporting what has happened, it's about preventing what could happen.

Looking for a reliable Pharmacovigilance partner or want to learn how we can support your organisation? We'd be happy to help. Contact us via: https://www.interdos.nl/contact-us/

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