Your project is complex with many moving parts - and often a great deal of risk and uncertainty. Devoting sufficient time and resources to the early clinical development phase is crucial for overcoming obstacles and executing each step successfully.
With a 15-year history in R&D and regulatory consulting, and a staff with 120+ years of combined experience in nutritional science, clinical trials, and pharmaceutical development, Nutrasource takes a project management approach to help our clients maximize their investment and gain market access with the highest quality data possible.
Our project management model provides you with a dedicated technical Project Manager serving as a single point of contact to support your regulatory and clinical needs as your project unfolds. Our Project Managers have over 10 years of experience in nutrition research, regulatory affairs, and/or the pharmaceutical industry. Through a true partnership, our team will work with you to develop the project plan, determine timelines, achieve milestones, facilitate communication, and provide deliverables in a timely, cost-effective manner.
Find out how we can help you manage your clinical or regulatory project from concept to claim.
Case Study: Complex Multi-Ingredient Products Can Be Effectively Studied to Ensure Optimal Dosing for Future Studies
Learn how Nutrasource assisted a Sponsor in determining optimal dosing.
Case Study: A Multi-Centre Clinical Trial to Determine the Efficacy of an Omega-3 Medical Food in NAFLD
Learn how we helped one Sponsor gain market entry for a medical food with a unique health claim.