A roundup of manufacturing and service expansions.
A roundup of manufacturing and service expansions.
New York (Aug. 20)—ImClone Systems received approval from the US Food and Drug Administration for its second facility to manufacture "Erbitux" (cetuximab). The approval to manufacture Erbitux in the new 250,000-ft.2 multisuite manufacturing facility, referred to as BB50, more than doubles ImClone's total available production-volume capacity.
San Diego, CA (Aug. 16)—Pharmatek Laboratories added cytotoxic and high-potent drug development capabilities to its pharmaceutical chemistry development services. Cytotoxic and high-potent services include analytical method development, preformulation testing, formulation development, manufacturing for early-phase clinical trials, release testing, and stability testing and storage.
Cramlington, UK (Aug. 23)–Aesica opened its new pilot plant at Cramlington to manufacture and supply small-scale quantities of clinical compounds (10–100 kg).
Toronto, ON, Canada (Aug. 13)—Microbix Biosystems established a team of experts to help manufacturers boost their production of influenza vaccine. The "Special Workgroup for Applied Technology Transfer" or "SWATT" group, working with the company's "VirusMax" technology, spends several weeks at each facility to help implement the technology and train personnel.
The VirusMax technology is designed to increase the virus yield from eggs by effectively recovering the virus. "Our technology can be installed very quickly, and with limited capital costs into existing manufacturing processes," said William J. Gastle, CEO of Microbix, in a prepared statement. According to the company, the technology has been shown to double vaccine production.
Mississauga, Ontario, Canada (Aug. 1)—Alphora Research recently expanded to include a 14,000-ft2 facility to support a new pilot-plant facility. The pilot-plant is currently under construction and is targeted for completion by the end of 2007. This facility includes 200-L and 400-L glass-lined reactors, which includes equipment for cryogenic reactions. Support functions are also being installed, including warehousing and quality control capabilities.
Kankakee, IL (Aug. 1)—CSL Behring will invest $15 million to expand its manufacturing facility by adding a high-speed, single-dose syringe-filling line. Plans call for the line to be operational in 2010, when the company intends to contract with its sister company, CSL Biotherapies, to provide filling and packaging services for seasonal influenza vaccine.
Why is the PDA Pharmaceutical Microbiology Conference the Hottest Ticket in the Industry?
October 10th 2024Get a glimpse of the power and popularity behind the PDA Pharmaceutical Microbiology Conference from two planning committee members, Julia Marre, PhD (Associate Director, Scientific and Regulatory Affairs at Pocket Naloxone Corp) and Dawn Watson (Executive Director, Global Micro Quality and Sterility Assurance at Merck). This candid conversation reveals why this industry event is so influential…and always sold out! The speakers discuss what makes the PDA Pharmaceutical Microbiology Conference so vital to industry professionals, as well as how to become a part of this dynamic professional community.
Navigating Annex 1 for Early Phase Sterile Fill Finish in Clinical Supplies
November 21st 2024Stay compliant with Annex 1 for early phase sterile fill finish processes. Discover how to implement robust contamination control strategies, integrate isolator technology, and conduct integrity testing to meet stringent European Union standards. The guide provides a comprehensive look at key elements such as PUPSIT, critical zone controls, and monitoring and training for aseptic processes.
Your Ultimate Guide for CMC Testing Support for Gene and Cell Therapy
November 21st 2024Explore the complexities of gene and cell therapy development with our comprehensive guide to Chemistry, Manufacturing, and Controls (CMC) testing. Learn how our expertise ensures the safety, potency, and quality of advanced therapies, supporting your journey from product development through regulatory approval.