- Sterilization Wrapping System
- Covers & Closures
- Cleanroom Problem Solvers
- Cleanroom Tools
- Powder Transfer Sleeves
- Sterile Cleanroom Apparel
Sterilization Wrapping System
For autoclave sterilization, we provide an unsurpassed assortment of component prep alternatives designed to save you time, increase compliance, and reduce risk of contamination.
Covers & Closures
GEPCO's Covers and closures fit machines, equipment, racks, carts and all sorts of small openings in your production area. Made from strong, durable Tyvek®, our extensive range of covers and closures protect all sizes of equipment, simplify conformance to SOPs, reduce cross-contamination and improve the appearance of your production area.
Cleanroom Problem Solvers
GEPCO has over 25 years of experience solving problems in aseptic processing areas, helping you improve your operations, increase regulatory compliance and enhance your adherence to cGMPs.
Powder Transfer Sleeves
GEPCO’s powder transfer sleeves provide a safe, clean way to move powders and other product between vessels, processing equipment and containers during production. Our sleeves are designed with inner skirts and other features to reduce cross-contamination and facilitate ease of use. They are specifically fitted to the exact mills, blenders, granulators and other equipment you use.
Sterile Cleanroom Apparel
Gowning and regowning present particular challenges in a sterile environment. GEPCO specializes in providing cleanroom apparel packs designed, assembled and packaged to facilitate adherence to gowning SOPs.
Sterile drug products produced by aseptic processing are the most stringently regulated and require maintenance of the highest-quality critical environment. Each manufacturing step requires validation and control.
A complete assortment of component prep materials is available to provide a comprehensive “system” solution for all autoclaved components. Bags, covers, tubing and wrappers of any shape or size can be provided to make this process the most efficient.
Tablets, Capsules and Liquids
Tablet, capsule and liquid manufacturing require many processes, each of which poses the possibility for product contamination or risk to personnel. Dispensing, granulation, drying/compaction, blending/mixing, milling, compression, coating and filling are among the critical steps in the production process.
Quality assurance is vital to all pharmaceutical and biotech manufacturing. Procedures followed by the microbiology testing lab ensure the integrity of the manufacturing environment and the product itself. Sampling, transportation, incubation, and sterility testing provide an opportunity for external contamination to skew or invalidate testing results.
API’s and Excipients
Chemical synthesis and natural extraction of active pharmaceutical ingredients, as well as production of excipients, are subject to expanding regulatory scrutiny. Compliance with current Good Manufacturing Practices (cGMPs) is vital to maintain product integrity and satisfy regulations.