Sampling Systems for the Pharmaceutical Industry

In regulated bioprocessing environments, materials must be biologically inert and fully compliant with applicable ISO and USP standards. Only GMP-compliant, validated sampling components ensure:

• Contamination-free sample collection
• Preservation of critical process parameters
• Audit readiness and data integrity
• Consistent and reproducible results

GMPTECs sampling accessories are designed to integrate seamlessly into existing processes, enabling safe, controlled, and contamination-free transfers throughout the sampling procedure.

Closed systems, which contain e. g. sampling bags already, mean a fully sealed unit between the process line and the sampling container. This design prevents any contact between the sample and the external environment, significantly reducing the risk of cross-contamination—particularly when handling sterile or sensitive media.

Reproducible sampling is achieved through the use of standardized adapters or assemblies, clearly defined sampling points, and precisely controlled valves. GMPTECs accessories guarantee consistent fluid handling, minimize process variability, and streamline operations—even in complex or sterile applications.

Safe and GMP-compliant storage is ensured through validated, tightly sealing sample bags and bottles crafted from media-resistant materials. Combined with a carefully engineered sealing system and materials optimized for storage and analysis conditions, this approach preserves the integrity and quality of samples throughout their entire lifecycle.