Axia Pharmaceutical is an FDA-registered, full-service 503B outsourcing facility. We manufacture the highest quality injectable medications using stringent processes to ensure product purity and patient safety. We adhere to all applicable cGMP requirements and meet or exceed USP Chapter requirements.
We use FDA-approved components and packaging containers to provide our customers with high quality and safe injectable pharmaceuticals. We use sterile processes at each stage of manufacturing, as well as rigorous in-house quality assurance and quality control procedures to ensure that our customers receive the highest quality medications every single time.
We use FDA-approved components and packaging containers to provide our customers with high quality and safe injectable pharmaceuticals. We use sterile processes at each stage of manufacturing, as well as rigorous in-house quality assurance and quality control procedures to ensure that our customers receive the highest quality medications every single time.
Services
We are an FDA-registered outsourcing facility that works closely with patients, physicians and hospitals. Axia Pharmaceutical's outsourcing facility makes a variety of products for all clients, from single patients to office use. We can custom-create any injectable medication as long as it has a USP/NF Monograph or equivalent, i.e.
Our state-of-the-art facility contains all of the modern technology necessary to provide our clients with pure injectable pharmaceutical agents of the highest quality. A completely sterile workspace with badge-only access, with barrier separation between internal and external environments. A USP800 clean room that has been installed for the preparation of hazardous medications well before the the 2018 FDA-mandated deadline.
Axia Pharmaceutical Complies with All cGMP Requirements Mandated for Outsourcing Facilities. Current good manufacturing practices, or cGMPs, are a series of regulations established and enforced by the FDA to ensure the quality and safety of pharmaceuticals. They ensure the identity, quality, strength, and purity of pharmaceutical products by requiring manufacturers to control their manufacturing facilities and processes adequately.
We follow several strict in-house Quality Assurance and Quality Control (QA/QC) procedures to ensure that all of our products are completely sterile and safe before distribution to the client. These processes are overseen by our full-time QA/QC manager, who works closely with FDA consultants to ensure that we not only comply with all FDA regulations, but that we exceed these requirements.
Reviews
Be the first to review Axia Pharmaceutical.
Write a Review
