Globalization and free trade explosion have changed the way individuals today access medicinal products. Pharmacovigilance Drug Safety is the fundamental cornerstone for ensuring patient safety in clinical development and post authorization for medicinal products. With global regulatory authorities giving drug safety more and more importance, the need to have a robust Pharmacovigilance system in place is vital for an organization. Accurate and responsible monitoring of adverse events and risks observed during clinical development as well as post marketing is mandatory and in the best interest of patients, subscribers, payors and sponsors.

However, resources and specialist know-how of marketing authorization holders might be limited, or company-internal pharmacovigilance department already suffering from highly stretched resources.

The expertise and flexibility provided by PharmaCons PhVC can complement current activities or provide an entire team without the need to hire individual staff members.

Clinical Trials

Life Sciences

Medical Devices

Pharmaceutical

PharmaCons PhVC

PharmaCons PhVC's headquarters in Bucharest, Romania

Adina Anghel

Oana Rebedea

Claudiu Ciortea

This department is responsible for monitoring the safety and efficacy of pharmaceutical products, ensuring compliance with regulatory requirements, and managing adverse event reporting.

Pharmacovigilance

This department focuses on the evaluation and management of medical information and safety within clinical and regulatory contexts.

PharmaCons PhVC

Org chart

Teams

Pharmacovigilance

Medical Affairs

Offices

PharmaCons PhVC

Org chart

Teams

Pharmacovigilance

Medical Affairs

Offices

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