USP 797 Sterile Compounding

Edge Pharma produces sterile compounded medications for a wide array of medical specialties including dermatology, ophthalmology, urology, pulmonology, anesthesiology, allergy, ENT, OB/GYN, and several others. Edge specializes in developing unique and creative solutions to solve compliance challenges.

Within the Edge Pharma facilities, USP 797 and CGMP requirements form the foundation upon which safe production is achieved. Edge helps meet the demands placed on your institution to ensure your medications are in stock when you need them. Safety is built into our processes, giving you confidence that you are providing the best option for patients.

  • Edge Pharma follows USP 797 standards and CGMP requirements utilizing FDA approved and USP grade components and sterile containers.
  • World-class team of scientists, pharmacists, engineers, technicians, and support staff ensure every step of the process, from component intake through final quality check, meets both internal and regulatory standards.
  • Full chemistry and microbiology labs, staffed by PhD level scientists, provide support through both the product development process, as well as routine batch testing, for example sterility, potency, and endotoxin.
  • Ready-to-use unit doses mean your organization can feel comfortable that safety is the top priority.
  • Many of our products are sealed with tamper-evident caps, UV-resistant safety over-wrap bags, and proprietary shrink sleeves for added protection.

Allergy Compounding

Otolaryngology (ENT)