BioPoint assists life science organizations of all sizes reach their goals on time. Our engagement philosophy is simple: “Within scope, on time, under budget.” Review a sample of case studies below of real-life clients utilizing BioPoint’s just-in-time methodology
At BioPoint we understand the importance of properly navigating a complex global regulatory arena.
Our interdisciplinary network of clinical development experts is available to support our clients at every phase of product development.
BioPoint’s HEOR Consulting services are relied upon by small and large Pharmaceutical, Biotech, and Medical Device organizations in need of deep focused knowledge around HEOR.
BioPoint has a team of experienced and knowledgeable quality assurance experts that can help you create a clinical quality process and system, or, objectively assess existing clinical quality systems.
BioPoint's wide range of Medical Affairs experience and expertise enables us to provide effective consulting solutions to support and ensure the successful launch of new medical treatments and drugs to patients worldwide.
Drug Safety & PV
BioPoint has the broad-based experience to provide comprehensive clinical and post-marketed drug safety and pharmacovigilance consulting services to help you address product safety concerns in a confident, proactive manner.
BioPoint’s customized offerings include both strategic leadership and tactical support within the Regulatory, Quality, Clinical, Safety & Surveillance and HEOR / Market Access functions.