Pharmacovigilance services
ReturnPharmacovigilance is critical to ensuring patient safety from clinical studies to post-marketing phases.
At Tiofarma, we offer comprehensive support during all these phases, adhering to European regulations.
We understand the critical role of pharmacovigilance in developing drug products from clinical stages to post-marketing, aiming to identify, understand, and prevent adverse effects. We collaborate closely with long-term external partners to ensure compliance with European pharmacovigilance regulations, providing extensive support as needed. Our expertise includes creating and maintaining Pharmacovigilance System Master Files (PSMF) and Risk Management Plans (RMP). Tiofarma is committed to daily product safety monitoring and regulatory compliance throughout the product lifecycle.
