Manufacturing

Patricia Van Arnum was executive editor of Pharmaceutical Technology.

Articles

A recent market analysis offers a promising outlook for contract fill-finish and lyophilization services.

Strong Prospects for Fill-Finish Contract Manufacturing

CentuRecon enables dry formulations of therapeutic proteins to quickly be prepared for injection at high concentration.

XstalBio Introduces CentuRecon

RABS is a flexible barrier system that maximizes product control but minimizes operator interaction when best practices are followed.

Best Practices for Restricted Access Barrier Systems in Aseptic Manufacturing

Susan Schniepp, vice-president of quality and regulatory affairs at Allergy Laboratories and co-chair of the program planning committee for the 2013 PDA/FDA Joint Regulatory Conference, discusses quality systems and related considerations in parenteral drug manufacturing.

Focusing on Quality for Parenteral Drug Manufacturing

New cartridges designed specifically for use on high-speed filling lines increase efficiency.

New Cartridge Technology for High-Speed Filling in Parenteral Drug Manufacturing

Report outlines recommended practices for control and evaluation of operations.

Parenteral Drug Association Releases New Report on Manual Aseptic Processes

A screening method aligned with USP 1660 guidance predicts glass delamination in primary packaging for parenterals.

Evaluating Parenteral Packaging for Glass Delamination

Cynthia A. Challener is a contributing editor to Pharmaceutical Technology.

The benefits of single-use systems are being realized for downstream unit operations, including aseptic filling.

Aseptic Filling is the Next-Generation Application for Single-Use Systems

Aseptic connectors provide the flexibility and robustness needed for modern parenteral manufacturing operations.

Will Aseptic Connectors Make Production Outside of the Cleanroom Possible?

Adoption of single-use systems and more flexible systems drive innovation.

Manufacturing, Parenterals and Injectables