At Boyds, our goal is to facilitate the translation of cutting-edge science into medicinal products which benefit patients. 

We understand how challenging this can be, both technically and commercially. 

Our service is designed to provide crucial experience and assistance whenever you need it, in order to bring your innovations to the marketplace as quickly and efficiently as possible.

Boyds was established in 2005 and provides a range of expertise and skills central to the development of pharmaceutical and biotechnology medicinal products and medical devices.

We are headquartered in the UK with offices located in Cheshire and Cambridgeshire and also have offices in Dublin and Pennsylvania.

Our consultancy services offer a cost-effective solution for those requiring expert assistance in order to expedite development, add value to their product, and reach those key milestones.

Whether it relates to a single issue or a long-term commitment to your development team, we can help you chart the innovative course great science demands.

Biotechnology

Life Sciences

Pharmaceutical

Boyds

Alan Boyd

Nicholas Meyers

Neil Fish

Karen Mullen

Julie Warner

Neil Chakrabarti

The Regulatory Affairs team at Boyds navigates the complex regulatory landscape to ensure pharmaceutical and biotechnology products meet all required standards and regulations for market approval. They provide expert advice and manage regulatory submissions to expedite the development process, ensuring compliance and aligning strategies with both global and local regulatory requirements. This team plays a crucial role in facilitating the successful and efficient translation of innovative science into marketable medicinal products.

Regulatory Affairs

Leadership Team

Regulatory Affairs

About

Team members

Other teams at Boyds

Leadership Team