BioMDg is a unique consulting group comprised of a core team of Preclinical, Clinical, Regulatory and Marketing professionals closely aligned with a network of experts with proven track records in multiple areas of science, medicine and new technology marketing. We use a global comprehensive approach to bring products to market early.
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Our core competencies include:
- Regulatory Strategies and Submissions (incl. IDEs, INDs, PMAs, 510(k)s and European Submissions)Clinical Trial Design and, Submission, Oversight, and Analysis – including full CRO services, DSMB management, IRB/IBC submissions, and submission of gene therapY studies to the Recombinant DNA Advisory Committee at NIH
- Preclinical Study Design
- Critical Literature Reviews
- Scientific Business Plans – for Venture Capital Funding Due diligence and Valuation of New Technologies Hazard and Risk Analysis
- Post Marketing Study Designs
- White Papers
- Continuing Education & Training
Contact BioMDg
20370 Skyhawk Lane
Topanga, CA 90290
info@biomdg.com
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