Clinical and Medical Affairs
Boyds' expert Clinical and Medical Affairs Team supports clients in all aspects of drug development and regulation, offering clients the bridge between industry and the wider medical community.
Good Clinical Practice (GCP) mandates all clinical studies to have medical oversight to ensure patient safety and study compliance. Boyds’ team of experienced pharmaceutical physicians provides medical monitoring across a wide range of study types and therapeutic areas including early-phase studies, advanced therapies, and orphan drugs.
Our experienced physicians dedicate time to reviewing and advising on the study design and documents. They work closely with sponsors, investigators and sites ensuring smooth and timely recruitment, patient safety and data integrity for the duration of the study through to close out.
Boyds experienced Clinical and Medical Affairs Team can assist clients with clinical product development by providing:
- Medical advice
- Risk management plans
- Assist in the design of clinical trial protocols
- Product commercialization support including Medical Affairs (e.g. drafting and review of promotional materials)
- Clinical overviews
- Independent medical monitoring
Find out more about clinical and medical affairs services from Boyds.
Get in touch
If you would like to talk to a member of our team about a specific project or area of expertise, then please complete this form and we will get in touch.
