Veleka R. Peeples-Dyer, is an experienced lawyer with an extensive background in the life sciences industry, advising biopharmaceutical companies on FDA regulatory and global compliance matters.
Veleka counsels clients on regulatory and compliance matters throughout the product lifecycle, including clinical trials and current good clinical practices (GCP), product launch and commercialization, pharmacovigilance, current good manufacturing practices (GMP), supply chain, due diligence, licensing and FDA inspections, compliance and enforcement actions.
Veleka also advises legal and compliance professionals on developing, implementing and enhancing corporate compliance and ethics programs to address a broad range of issues, including advertising and promotion, product safety and adverse event reporting, patient advocacy programs, speaker programs, and federal and state transparency and disclosure, including the Federal Physician Payments (“Sunshine”) Act. She has handled significant governmental and internal investigations and designed and implemented both corporate-wide and brand-specific compliance programs and policies.
Veleka is a graduate of Hampton University and the University of South Carolina School of Law.
