Bringing a new medical technology to market can be a lengthy, expensive, and complex process. Poorly developed protocols, inadequate management of clinical trials, deficient regulatory submissions, and stalled FDA negotiations are just a few of the roadblocks that can cause costly delays, even cancelled projects.

At Boston Biomedical Associates, we provide medical device and biomedical companies with comprehensive, proven methodologies to help bring new technologies to market – only more efficiently. We developed Med•D4™, a quality driven, multi-modular program designed to:

Define regulatory and clinical strategies
Develop clinical research and data management processes
Document the submission process
Deliver the product approval process

Comprehensive Services
• Regulatory strategy and submission preparation
• FDA liaison
• Clinical trial design, management, and monitoring
• Data management and biostatistics
• Quality assurance/compliance
• Quality audits/training
• Venture capital investment counseling

Using our proven Med•D4™ program, our experienced expert staff can help you take your medical technology frm concept through FDA to market approval.

Contact Us
Call our Massachusetts office at 866-351-8632 (In MA 508-351-8632)
M-F 8-5 eastern time or e-mail us and we’ll contact you directly.

BOSTON BIOMEDICAL ASSOCIATES
386 West Main Street, Suite 7 · Northboro, MA 01532
Tel. (508) 351-8632 · Fax: (508) 351-8637

©2007 Boston Biomedical