A Global Partner for Medical Device Clinical Studies
BBMCT Medical Device specializes in medical device and diagnostic clinical development. Streamline your path to success with a CRO that knows the unique demands of medical device and diagnostics clinical trials. Our medical, regulatory and operational experts work collaboratively with your team to design and conduct clinical research trials around the world. We apply everything we’ve learned throughout our extensive experience conducting pre- and post-marketing medical device clinical studies across many therapeutic areas to your study. You’ll work with teams who specialize in your specific therapeutic area and who understand and have overcome the challenges you face.
Reimagining global health one solution at a time.
The constant in the biopharmaceutical industry is change. And as science catapults forward, our Medical and Scientific Services team is ready to help you lead the way by constantly reimagining how therapies are developed, while never losing sight of patients. Our collection of services is carefully structured to equip you to navigate new ways of working.
Engaging across audiences.
Translating your data into effective communication does more than get a point across. When done correctly, it shows who you are at your core – and engages and inspires action. Regardless of the size of your project, our writers and strategists carefully craft your messaging with the end audience at heart – from regulatory bodies to the volunteers driving your project ahead.
British BioMedicine Clinical Trials (BBMCT)
A Global Partner That Understands Your Needs
Our global presence and experience means more than just having feet on the ground. Our geographically diverse and multilingual employees understand the local cultural environment for clinical research and your regulatory pathway:
- Established relationships with clinical research sites, key opinion leaders and therapeutic networks experienced in medical device trials allows BBMCT to select the ideal geographies and sites to ensure key milestones are met
- Regulatory affairs staff provide guidance in selecting the optimal regulatory pathway and have the experience to coordinate and lead meetings with FDA and EU notified bodies
- Multilingual staff ensure your program is interpreted and implemented efficiently and appropriately
- Our unique model provides therapeutic and scientific leadership throughout your program’s lifecycle
We apply everything we’ve learned throughout our extensive experience conducting pre- and post-marketing studies across many therapeutic areas to your study. You’ll work with teams who specialize in your specific therapeutic area and who understand and have overcome the challenges you face.
