Hot Topics

Biopharmaceutical Technology Transfer

Introduction Technology transfer happens during the production life-cycle of biopharmaceuticals. Technology transfer can take place internally within a biopharmaceutical company from the process development to manufacturing teams, from one site to another site, or from […]

Aseptic Connection and Disconnection

Single-Use Aseptic Connectors

Sterile connection are critical requirements in any aseptic process operations. The benefits of using pre-sterilized single-use systems can only be realized when the products and components can provide safely and securely connection for fluid handling […]

Aseptic Connection and Disconnection

Single-Use Aseptic Disconnectors

Various single-use sterile disconnectors are available in the market to provide secure, quick disconnection of sterile unit operations for higher operating efficiency and process reliability. Quick-disconnect coupling or fittings (sanitary design and luer-lock design) are […]

Aseptic Connection and Disconnection

Tubing Sealers

Biopharmaceutical manufacturing process often need retain and store samples or bioprocess fluids, and tubing in the bag assemblies or manifolds must be permanently sealed without breaking sterility. Heat sealer adhere tubing inner wall to inner […]

Container, Closures and Assemblies

Primary Packaging

Delicate biopharmaceutical products often need advanced packaging features to protect them from moisture, light, oxygen, and contaminants. Pharmaceutical primary packaging materials are defined as packaging materials that are in direct contact with the pharmaceutical product, […]

Container, Closures and Assemblies

Single-use Lyophilization Products

Freeze drying or lyophilization is a method for preserving a wide variety of heat-sensitive materials such as media, proteins, microbes, pharmaceuticals final products, these products are presented as a freeze-dried powder in vials for reconstitution […]

Container, Closures and Assemblies

Freeze/Thaw Solutions

Sensitive pharmaceutical products, whether for clinical development or large scale commercial manufacturing final drug products, often need to be frozen to maintain their stability, quaility and extend shelf life. Freezing decreases the risk of microbial contamination […]

  • Filter Housing and Equipment

    As the biopharmaceutical industry filter products evolves and matures, so do the materials and designs of filter housing and peripheral equipment. Sanitary filter housing has tranditionally been built of 316L or 304L stainless steel, typical [...]
  • Viral Filtration

    Biopharmaceutical manufacturing using mammalian cell culture must have processes in place to minimize the likelihood of virus contaimination and demonstrate the virus removal capabilities. Regulatory authorities expect purification processes to include multiple steps with complementary, [...]
  • Tangential Flow (Cross Flow) Filtration (TFF)

    Tangential Flow Filtration (TFF), also called Cross Flow Filtration (CFF), is a rapid and efficient method for filtration and separation of bioprocessing fluids. In tangential flow system configuration, the particels or containments thar are too [...]