Pharmaceutical consulting: discover our expertise

The pharmaceutical industry is one of the most complex industries, involving multiple stakeholders and processes. From the discovery of novel drugs through the clinical trials and approval process to market authorization, ensuring regulatory compliance is critical.

Regulatory Affairs is an essential function within pharmaceutical companies, where it plays a vital role in ensuring safe and effective medicines reach patients. This function includes managing the entire lifecycle of a medicine from discovery to marketing authorization, including post-marketing surveillance and vigilance.

ProductLife Group offers comprehensive solutions for pharmaceutical companies looking to streamline their operations and maximize efficiency. We help our clients navigate the complex landscape of pharmaceutical regulation, working closely with them to ensure that their products receive timely approvals and meet strict regulatory requirements.

We help pharmaceutical, biotechnology, and healthcare organizations develop their drugs, biologics, devices, and other medical products through innovation and global regulatory services.

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ProductLife Group’s objective is to be at the forefront of every aspect of regulatory compliance—both now and in the future.

Xavier Duburcq

CEO

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" Regulatory insights every biotech founder needs to know (before first-in-human trials) "

An online event

05 june 2025 - 05 june 2025

16:00

" EUDAMED – Are you ready for the gradual roll-out? "

An online event

15 may 2025 - 15 may 2025

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" Raps Euro Convergence 2025
A live event in Brussels "

13 may 2025 - 16 may 2025