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Optimise your PV operations through monitoring and use of technology by our SMEs.

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Come to rescue of your PV systems during service provider modifications or technology switch.

PVBridge™

Help our long-standing clients to develop in-house pharmacovigilance capacity.

PVIntegrate™

Streamline your PV systems and processes during expansion.

PVExpert™

Strengthen your negotiations with regulators, HTAs and external stakeholders.

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Comprehensive PV management of seasonal vaccines ICSRs and systems to enable seamless end-to-end operations.

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Our experts can advise you on your vigilance system, post-market surveillance and safety reporting.

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Support tailored PV research in pediatrics and draw lessons from risk minimization of ARs in adult population.

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We adjust your RMPs cognizant that co-morbidities or side effects - specific to older patients - will shape PV activities.

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Quality & CAPA Management

Overview of the ISO Identification of Medicinal Products (IDMP) Standards

Published: 21 February, 2023

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Exploring the Crucial Role of Local Persons for Pharmacovigilance on a Global Scale

The essential role of local person in ensuring effective pharmacovigilance worldwide

Published: 4 May, 2023

Duration: 19 Mins

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Press Release – Panacea Pharma Projects Limited rebrands to PrimeVigilance

Published 16 July 2024

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World Drug Safety Congress Europe 2024

Published 9 September 2024

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NEWS: DIA Safety Management Plan Workshop with Dr Jan Petracek in China, July 10 -11 2017.

PrimeVigilance is pleased to announce that Dr. Petracek will be teaching in China at the DIA Safety Management Plan Workshop.

This two-days intensive training course is organized by DIA on July 10 – 11, 2017 in Beijing, China.

The agenda was prepared with the aim to bring the latest information from European to Chinese Pharmacovigilance and Regulatory Affairs Professionals on the following topics:

Legal possibilities for benefit optimisation and risk minimisation of products in the EU
Designing benefit-risk management systems using current regulatory tools, including EU Risk Management Plans (EU-RMPs), Development Safety Update Report (DSUR), Periodic Safety Update Report (PSUR)
Best study designs for safety and efficacy follow-up, and how to measure their effectiveness

Dr. Petracek is an internationally known pharmacovigilance expert with a long history of professional trainings and speaking courses for DIA events worldwide. He is scheduled to cover seven sessions out of thirteen sessions which are on the agenda of this training course.
For the agenda and registration details please visit the DIA website.
If you are interested in an on-site private meeting with Dr. Petracek, we will be glad to arrange it for you, please contact us.