Headquarters:
regenold GmbH
Zöllinplatz 4
79410 Badenweiler
Germany
Phone: +49 7632 82 26-0
Fax: +49 7632 82 26-555
Email:
info@regenold.com
Associate Director, Pharmacovigilance
Andrew joined regenold in September 2025 and has close to 20 years of experience in the pharmaceutical industry, with a proven track record in pharmacovigilance and drug safety. Andrew has more than 15 years of experience in all aspects of pharmacovigilance, both in clinical research and post marketing surveillance. In addition, Andrew has close to 4 years of experience as a UK Qualified Person for Pharmacovigilance (UK QPPV).
Andrew has an established history of providing strategic oversight and pragmatic, sensible solutions to ensure compliance with global pharmacovigilance requirements and regulations. His dual experience at clinical research organisations and within industry affords Andrew the ability to create a broad range of delivery models for clients.
Andrew holds an Honours Degree in Forensic Science from the University of Glamorgan, Wales. In his spare time, he enjoys travel, playing golf and spending as much time as possible with family and friends
What does a Pharmacovigilance (PV) consultant actually do all day?
It's a question we get asked a lot. And the answer might surprise you. No two days are the same.
At regenold our PV consultants balance regulatory expertise, operational support, and strategic thinking, often all in a single day.
The day often starts with reviewing regulatory updates and ongoing projects.
PV consultants interpret and apply evolving legislation and guidance, such as EU GVP Modules, helping companies stay compliant without overcomplicating their processes.
This might involve:
A large part of the role is designing and optimising pharmacovigilance systems.
In practice, this can include:
This is where consultants add real value, not just ensuring compliance, but making systems more efficient and scalable.
Some days require rolling up our sleeves.
PV consultants often step in to provide short-term operational support, especially for organisations with limited internal resources.
This might involve:
For smaller biotech companies or virtual organisations, this support can be critical.
Another key part of the role is helping clients prepare for audits and inspections.
This includes:
The goal is not just to pass inspections, but to build confidence in the PV system.
At a senior level, PV consultants also provide strategic oversight.
This can mean:
PV consultancy is especially valuable for:
A PV consultant isn't just an extra pair of hands.
They bring experience, perspective, and flexibility, helping organisations navigate complex regulatory environments while building systems that actually work in practice.
Whether you need short-term operational support, strategic oversight, or help preparing for an inspection, regenold can step in exactly where you need us.
Our consultants integrate seamlessly with your team, bringing practical, hands-on expertise without unnecessary complexity.
If you're looking for a PV partner who understands both compliance and real-world delivery, get in touch with the team at regenold to start the conversation.
Get in touch with us to find out how regenold can strengthen your pharmacovigilance function.
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