In the interest of safety, purity, and effectiveness, pharmaceutical manufacturing industries must comply with the FDA’s Good Manufacturing Practices (cGMP). Validation is a critical part of ensuring that regulations are followed and the costly consequences of non-compliance and risks of cross-contamination are avoided.
APPLICATIONS
CHALLENGES
Recommended Cleaning Solutions for Aseptic Fill Operations
| Product Family | Part # | ISO Level | Material | Process Benefits |
|---|---|---|---|---|
![]() | TS2PUI70P-99S | 4+ | TekniClean® Presat, Sterile Polyester Knit Sealed Edge |
|
![]() | TC2P12S-LE | 4+ | TekniClean®, Sterile Low Endotoxin Polyester Knit Sealed Edge |
|
![]() | TC2MFUW-99S | 4+ | MicroClean™ Sterile Microfiber Woven Sealed Edge |
|




