Biomedical Development Corporation
Founded in 1984, Biomedical Development Corporation (BDC) focuses on achieving superior clinical outcomes through innovative products and collaborative partnerships with recognized scientists. They specialize in bringing new medical technologies from development to commercialization, utilizing a unique, capital-efficient business model funded by non-dilutive government grants, primarily NIH SBIR/STTR awards. Their expertise spans grant writing, clinical trials, regulatory filings, manufacturing, and formulation development, aiming to connect breakthrough technologies with consumers efficiently.
Industries
Nr. of Employees
small (1-50)
Biomedical Development Corporation
Lexington, Kentucky, United States, North America
Products
Overnight breathable topical masque (patented technology)
A topical overnight breathable facial masque developed from proprietary formulation technology and produced through the company's development processes.
Iodine-based oral rinse
An iodine-containing mouth rinse formulated for oral cleansing applications; subject of media coverage and planned studies.
Clinical software platform for bipolar disorder (under development)
A software analytics platform designed to support management of bipolar disorder; currently in development.
Overnight breathable topical masque (patented technology)
A topical overnight breathable facial masque developed from proprietary formulation technology and produced through the company's development processes.
Iodine-based oral rinse
An iodine-containing mouth rinse formulated for oral cleansing applications; subject of media coverage and planned studies.
Clinical software platform for bipolar disorder (under development)
A software analytics platform designed to support management of bipolar disorder; currently in development.
Services
Bench-scale formulation work through scale-up to manufacturing for topical and oral products.
cGMP production supported by quality management systems and laboratory facilities.
Design and conduct of clinical studies in compliance with Good Clinical Practice.
Preparation and filing support for regulatory applications including IND and 510(k).
Preparation and management of proposals for non-dilutive government funding and associated program administration.
Advisory services to move technologies from research through commercialization, including industry-scientist partnership facilitation.
Bench-scale formulation work through scale-up to manufacturing for topical and oral products.
cGMP production supported by quality management systems and laboratory facilities.
Design and conduct of clinical studies in compliance with Good Clinical Practice.
Preparation and filing support for regulatory applications including IND and 510(k).
Preparation and management of proposals for non-dilutive government funding and associated program administration.
Advisory services to move technologies from research through commercialization, including industry-scientist partnership facilitation.
Expertise Areas
- Clinical trial management
- Regulatory compliance and submissions (IND/510k)
- Formulation development and scale-up
- GMP manufacturing and quality systems
Key Technologies
- Good Manufacturing Practices (GMP)
- Formulation chemistry
- Digital health / clinical software platforms
- Clinical data management and GCP-aligned study operations