Daniel Solorio Email & Phone Number

A regulatory affairs and drug development executive with over 25 years of experience spanning the pharmaceutical R&D spectrum from program design and feasibility assessment to dossier development, regulatory submission and post-marketing studies. Experienced leading high-performance operations and regulatory teams through both early and late phase development activities including clinical development programs, compliance and quality initiatives, FDA meetings, IND/NDA/BLA submissions, product approvals, launches and postmarketing efforts, including promotional review. Also experienced in medical affairs activities including scientific communication, publication planning, HCP/KOL interaction and speaking/presenting at scientific conferences and advisory board meetings. Currently S.V.P. of Regulatory Program Management at ProPharma Group, leading the company's US Regulatory Program Management team and providing strategic clinical and regulatory affairs input and support to PPG's pharma, device and biotech clients.

Listed skills include Clinical Development and Regulatory Submissions.