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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Latest news

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24 june 2025 - 26 june 2025

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" Food Supplements Forum 2025 "

An online event

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" Innovative medical device start-up day "

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" BIO International "

16 june 2025 - 19 june 2025

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" AFI Symposium "

11 june 2025 - 13 june 2025

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" France Local Networking Group Virtual Event: Placing a Medical Device on the French Market: Get the Right Keys "

An online event

05 june 2025 - 05 june 2025

Europe 15:00