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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" Market Access Strategy for Device Reimbursement in Europe "

An online event

27 march 2025 - 27 march 2025

Europe 11:00

" Free Workshop: Preparing For Your Medical Device's Regulatory Strategy Plan "

In-person Event

17 april 2025

Europe 14:30

" Key Considerations When Building an LSO Program "

An online event

10 april 2025 - 10 april 2025

Europe 16:00

" EU Regulation 2024/1860: Interruption & Discontinuation of Medical Devices "

An online event

20 march 2025 - 20 march 2025

Europe 11:30