Discover How Strive Builds Quality Formulations

Trust in compounding has to be earned, and that means showing the work behind every formulation. In this live Strive Session, you’ll go inside the product formulation process, from scientific review and ingredient selection to prototype development, third-party testing, and ongoing quality assurance.

See how Strive evaluates pH, solubility, compatibility, potency, stability, and beyond-use dating while aligning formulations with applicable US Pharmacopeia (USP) standards. You’ll leave with a practical framework for assessing compounding partners, asking critical questions, and discerning compounding quality with confidence for your practice and patients.

This webinar is designed for healthcare professionals who want insight and understanding into the science and quality controls behind compounded formulations:

• Functional, integrative, and regenerative medicine providers
• Naturopathic doctors and wellness clinicians
• Aesthetic, longevity, and hormone health practitioners
• Practice leaders evaluating or working with compounding pharmacies

You’ll learn how to:

• Follow Strive’s formulation pathway from scientific review and ingredient selection through prototype development and quality assurance
• Understand how potency, sterility, endotoxins, stability, and other quality attributes are evaluated through appropriate testing
• Examine the controls supporting sterile and non-sterile compounded formulations, including pharmacist verification and technician competency testing
• Ask informed questions that help you evaluate a compounding pharmacy’s quality, transparency, and scientific standards