Aphena Pharma Solutions provides independent, third-party services in packaging and randomization for clinical studies. We have implemented rigorous procedures to assure total drug accountability and compliance with current Good Manufacturing Practices (cGMP) and Good Clinical Practices (GCP) regulations, standards and guidelines.
Aphena Pharma Solutions federal compliance history with the FDA, DEA and other governing bodies is very robust and has a solid foundation for all client needs. Aphena brings over 30 years of experience, knowledge, and thousands of third party successful cGMP audits to our clients. We believe quality and documentation controls are the key foundations of Aphena Pharma Solutions.
Securing Trust & Protecting Inventory
Millions of units-of-use per month can be processed through our fully equipped facilities. At the same time, Aphena ensures a small order will be treated with the same care and priority as a large order. Responsiveness includes communicating accurately and as often as the client desires. Through data exchange, clients can keep abreast of information at any point in the information stream. Precise tracking allows for identifying any item's location during the process.
Our Technology, Innovation & Experience
Aphena's capabilities expand to meet your specifications. The company's strength lies in management's ability to understand clients' unique environments and create dynamic solutions. Once products are ready to ship, Aphena handles distribution with utmost efficiency. Aphena is logistically and geographically positioned so that over 75 percent of the U.S. population can be reached within a day's drive, creating lower freight costs and supply chain simplification for our clients.