Edge's Quality lab and QC team are an integral part of the process. A combination of state-of-the-art equipment, testing logs, and full-time staff scientists ensure that every batch of medication delivered is both correct and safe.
Edge adheres to the values put forth by USP 795, 797, and CGMP. Through this our customers have the confidence in us to deliver medications they can feel comfortable administering, whether in a doctor's office or an operating room.
Located in Mississauga, Ontario, Edge is equipped with a system that monitors environmental controls and exceeds international standards for temperature, humidity, and sterility. Our facility is compliant with the following regulations and guidelines:
- USP 795, USP 797
- Ontario College of Pharmacists
- Health Canada
- Applicable Good Manufacturing Practice (GMP) Guidelines
Experience and Training
Each member of our staff undergoes rigorous training through skills certification, competency evaluations, and on-going education for QA, QC, Product Testing, Validation Testing, and Environmental Monitoring.
- Secure delivery and quarantine room layout and access
- Strict personnel gowning practices
- Precise sterile work preparation procedures
- Facility meets or exceeds USP 795, 797, and applicable CGMP standards.
Reliability and Service
Our facility is readily accessible for inspection and production monitoring by hospital, surgery center, and clinic customers. Customized formulation, delivery system, and labeling goes beyond standards to respond to the needs of your institution. Fast turnaround reduces drug shortages and eliminates the need to stockpile high-value drug inventories.