Expert in Pharmaceutical R and D
Helping you overcome technical and regulatory hurdles in drug development
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Experience and Technical Expertise
Highlights of drug development expertise
- Over 30 years of experience in R & D, from preclinical stage to submission, registration and post-marketing
- Serve on asset development teams in large pharma companies and collaborations with small and midsize companies
- Author and review of reports and submissions in support of regulatory filing and registration
- Design and oversight of nonclinical DMPK, toxicology programs
- Address regulatory queries and attend meetings with health agencies
- Conduct technical due diligence for asset inlicensing and M&A
- Design and conduct ADME & PK studies
- Selection and oversee CROs for ADME PK studies
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