We go the extra mile to safeguard our customers and their patients.
Avella’s FDA-registered 503B outsourcing facility maintains compliance with all cGMP requirements for safety and quality.
This focus on quality is embedded within all of our standard operating procedures:
- Our Arizona facility meets USP Chapter <797> and cGMP standards.
- Avella only procures sterile drugs and reservoirs from the most reputable, FDA-registered manufacturers—those with verified credentials and outstanding reputations for quality.
- Avella performs potency, sterility and endotoxin testing on all end-products.
- Our quality assurance team, which includes chemists, microbiologists, and pharmacists, oversees all the processes related to development and distribution of these products.
Our dedication to quality has been validated by a variety of outside organizations including our accreditation through the Pharmacy Compounding Accreditation Board. Avella was one of the first organizations to seek this accreditation, and less than 200 pharmacies in the nation share this honor.