Achievements
- 7 NDAs (1 Orphan Drug)/CTDs; 16 INDs, prepared/submitted and filed
- 3 BLAs prepared/submitted filed and or approved
- 1 PMA; 8 510K’s; 2 IDEs; 2 ANDAs, 2 CTx prepared/submitted and approved
- Multiple therapeutic areas track-record, i.e., cardiovascular, central
nervous system, dermatology hepatology, metabolism/endocrine, oncology,
thrombosis, nuclear imaging, antibioterrorism, etc.
- Successful orchestration of multiple manufacturing Sites (3 International)
for drug Substance/drug product managed through product launch and commercial
manufacturing
- International product investigation and recall (CAPA) management
- Speaker and regulatory trainer - Drug Information Association (DIA
-eCTD)
- ~$20 Billion Peak Annual Sales for Products Developed/Approved
- Acquisition of priority review, fast track, accelerated approval,
orphan drug, user fee waivers, etc.
- Successful manufacturing of “historical pharmaceutical development
products” for current submissions of genetically targeted clinical indications
- Reorganization of a major academic center including staffing, grants
and funding systems, and overall administrative functions according
to NIH and FDA quality standards
- Interim VP of Project Management, Regulatory and Quality Assurance
for the successful management of a pre-clinical rhesus monkey GLP study
for an international (China) anti-bioterrorism project-successfully
initiating preclinical monkey supportive care studies including hands
on training and quality systems development and translation to support
significant BARDA and DOD contracts
- Development of GMP systems for supplement and herbal manufacturers
to support changes in FDA guidelines for successful FDA audits
- Reversal of FDA clinical holds
- Published scientific author in professional journals
- COLOBIOSCIENCE Preferred Provider
Bridging Health
Matters Pamphlet