PrePak operates an FDA registered and DEA licensed (schedules II-V controls) pharmaceutical packaging and repackaging facility that provides turnkey solutions for a wide range of commercial services. It recognizes the high demand in the contract packaging industry for quality, tracking and security of pharmaceutical products. It has the capacity to streamline operations, reduce costs and ensure quality. PrePak's facility is equipped to fill the smallest to the largest commercial run.
Turnkey services allow clients to place inventory with confidence, minimize turnaround time and maintain just-in-time product quantities. PrePak stands ready to meet your commercial needs for:
| Bottling | Mail Order Facilitation | |
| Blister Packaging | Warehousing | |
| Unit Dosing | Re-Bulking | |
| Pouching | Private Label Design | |
| Kitting | Reworking | |
| Labeling | Fulfillment |
PrePak's facility encompasses 80,000 square feet under one roof, with 30,000 square feet dedicated for storage. It houses controlled environment rooms that meet or exceed FDA standards for cleanliness, temperature and humidity.
From fully automated fill lines to semi-automated lines, PrePak handles and processes small quantity orders of just a few bottles with the same care and priority as large quantity orders of thousands of bottles. PrePak fills custom orders that require special handling with clients setting the parameters.
PrePak has ePedigree software to combat drug counterfeiting and regulate supply chain visibility and security. Pedigree is a documentation process that enables a single view of a product's history for drug authentication. The pedigree tracks custody of the drug as it passes through the supply chain. The ePedigree software allows PrePak to comply with Florida, California and federal pedigree requirements while optimizing business operations with commercial customers.
PrePak's Control Systems Provide Security, Quality Assurance
PrePak quality control systems and pharmacists ensure proper oversight during all shifts. The flow of products through the facility is carefully controlled and monitored, maintaining the integrity of the process stream.
The company holds DEA (schedules II-V controls), GSA and Tennessee Board of Pharmacy licenses. The FDA's current Good Manufacturing Practice (cGMP) regulations dictate standard operating procedures. Extensive and ongoing cGMP training is standard company procedure. PrePak meets FDA standards for 21 CFR, Parts 210 and 211 for the processing, packing and holding of bulk drugs and finished pharmaceuticals.
A shelf-life control system monitors the hold time of materials shipped to the facility and awaiting repackaging. The labeling system gathers information throughout the process, and technology allows reporting of all information on demand to the client.
Precise tracking allows the company to identify each item's location during the process. A pill can be tracked from the time it is accepted into the warehouse until the time it is packaged and shipped.
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.
