BIOMEDICAL REGULATORY CONSULTING
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Careers

BRC seeks well-qualified experts to join BRC teams in preclinical, clinical, and CMC projects related to drug development and technical testing teams for medical devices, as well as eCTD support for submissions. 

Our clients are demanding, and our standards are high for cost- and time-efficient solutions to fulfilling complex regulatory strategies.  

Contact us should you have company or FDA experience or provide services in pharmaceutical regulatory affairs and/or medical device regulatory affairs. 

Thanks,
R.W. Soller, PhD
President, BRC

TELEPHONE

303.580.9208

FAX

888.370.5065

EMAIL

[email protected]
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  • HOME
  • Drug Development
    • Drug Development
    • The BRC Difference
    • Preclinical Consulting for Drug Development
    • Clinical Phases I, II, III
    • CMC Regulatory Affairs
  • Device Development
    • Med Device Development
    • Medical Device Regulatory Affairs Services
    • Medical Device Postmarketing Regulatory Services
  • Quality Management Systems
  • About Us
    • Mission & Objectves
    • Careers
  • Contact Us
  • For Entrepreneurs
  • All Services
    • Lists of BRC's Drug & Device Development Services