PharmApprove’s core service offering is our preparation of drug, biologic and device teams for high-visibility regulatory hearings in the US and Europe. Since its founding in 1999, the firm has managed 25 US FDA Advisory Committee projects in 15 disciplines, as well as four projects in Europe (three EMEA hearings and one appeal to Great Britain’s MHRA), providing everything from strategy, messaging, editorial, graphics, Q&A, presentation coaching and project management services.

In addition, PharmApprove also offers customized team training, “lessons learned,” and communications workshops for pharmaceutical teams who are not focused on regulatory approvals, but who seek ways to tangibly improve their communications with colleagues, clients, strategic partners and other target audiences. Those workshops include training in messaging, meeting management, presentation/public speaking skills, Q&A and other communications disciplines.