Bio-pharmaceutical systems must maintain sterility, containment, and regulatory compliance. Engineers test packaging, sterile containers, filters, and processing equipment to verify leak integrity and contamination control. They use vacuum chambers, helium leak detectors, and calibrated leak standards to support validation and process qualification.
Single-use bioprocess bags require rigorous leak testing to guarantee product integrity and prevent microbial contamination. Helium leak detection is used as the industry standard for detecting leaks in these systems, ensuring that the bags stay sealed and function as intended during use.
Reusable bioprocess containers used in biologic production and storage must maintain sterility and prevent contamination. Leak testing ensures that these containers remain intact and sealed during processing, ensuring the integrity of the biological products inside.
Package testing is essential for ensuring that packaging for biologics, vaccines, and pharmaceuticals remain intact and sealed during shipping and handling. Leak testing is performed to verify that packaging does not compromise the safety or sterility of the products.
Freeze drying is a critical process in the bio-pharma industry, used to preserve sensitive materials like proteins, vaccines, and biological samples. Vacuum systems are used to remove moisture while maintaining the integrity of the substance. This ensures long-term stability without compromising the quality of the product.
Cannabis extraction processes rely on vacuum to create the necessary pressure for efficient extraction of oils and concentrates. Vacuum systems are critical in maintaining the purity and stability of the extracted oils, while also preventing degradation of valuable compounds during extraction.
Vacuum storage is crucial for preserving sensitive materials like vaccines and biologics, extending their shelf life while maintaining efficacy. Vacuum systems are used to remove air and moisture, providing a controlled environment to protect the stored materials from degradation.
Vacuum testing for packaging is used to simulate pressure changes that may occur during shipping and storage. This ensures that the packaging maintains its integrity and that the products inside remain protected under varying environmental conditions.
Chillers are essential in cannabis extraction to maintain low temperatures during the extraction process, preserving the quality of the final product. They help regulate temperature fluctuations that could otherwise degrade sensitive compounds during extraction.
Perform fast, safe, and easy automated testing with the Allen Bradley PLC & HMI and included controls:
LACO’s unique standard platform single-use bag leak test systems include these key features:
Single-chamber or Dual-chamber systems
Choose between a single-chamber or dual-chamber system to meet your throughput requirements.
Allen Bradley or Siemens PLC
Choose which controller will be the best for your application.
Reliable product packaging is critical to prevent spills, contamination, and ensure product integrity during transportation. Issues such as packaging material compatibility, sealing machine setup, and contamination are factors that can affect the packaging seal reliability. Package testing in a vacuum environment can be a useful way of determining the integrity of product packaging.