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Company retrofits manufacturing facility for proprietary antimicrobial development

03/01/2005  EL CAJON, Calif.-PURE Bioscience (www.pure-bioscience.com) has begun conversion of part of its manufacturing space here to a dedicated, FDA-compliant, cGMP facility for production of pharmaceutical-grade silver dihydrogen citrate (SDC).

Setting the Standard: Evolution of an IEST Recommended Practice

03/01/2005  The Institute of Environmental Sciences and Technology (IEST) is responsible for the origination, publishing, and revision of approximately 35 Recommended Practices (RPs) in topics of interest and value to the contamination control industry.

The ABCs of disinfectant validation

03/01/2005  Despite ambiguities inherent in the regulatory inspection process, a few absolute expectations should be met

Your Market Analysis: Expanded role for life sciences cleanrooms

03/01/2005  Cleanroom technology developed for traditional applications such as aseptic filling in pharmaceutical plants is increasingly being applied to distinctly 21st Century problems.

Life Sciences: Personnel training

03/01/2005  The single most critical element of the cleanroom, or any controlled environment, is the human element.

From the Editor: The future is now

03/01/2005  A lot can happen in ten years. Certainly 2005 seemed a long way off when I wrote the editorial for the December 1994 special forecast issue of CleanRooms.

Process Analytical Technologies (PAT) and nonviable particle counting

03/01/2005  Pharmaceutical manufacturing environments have traditionally seen particle counting as a necessary evil to demonstrate compliance with a cleanroom standard.

The 'quietest' lab: Achieving vibration control and balanced design at NIST

03/01/2005  Engineers, lab planners and scientists developed unique lab layouts with groundbreaking temperature and vibration controls

Class 10,000 cleanroom provides more efficient, cleaner packaging suite

03/01/2005  ATLANTA, Ga.-When Celliance Corporation, a Serologicals company headquartered in Atlanta, Ga.

Relevant information for manufacturing quality control: A singular solution to a multi-industry problem

03/01/2005  Take a tour of manufacturing in the world today and you will encounter widely varying levels of sophistication across a broad spectrum of industries.

Moving Toward Automation

03/01/2005  During last fall’s much-publicized case of flu vaccine contamination at Chiron Corp.’s Liverpool, U.K., manufacturing facility, the Food and Drug Administration’s Center for Biologics Evaluation and Research (FDA CBER; www.fda.gov) issued a warning letter to the company that summarized numerous deviations from current good manufacturing practices (cGMP)-including several aseptic processing sterilization failures.

Choosing the Right Thermal Interface Material

03/01/2005  In the thermal management of microelectronics, the interface material layer between a chip and heat spreader presents the single largest barrier to heat flow in the packaging of high-power dissipation devices.

The Challenges of Qualifying ‘Green’ Packages

03/01/2005  NEW MATERIALS AND FAILURE ANALYSIS

Sawing Silicon

03/01/2005  The Art & Science of Wafer Dicing

Making It Practical

03/01/2005  There are dreamers and schemers, but rarely are both qualities so evident as in the world of advanced packaging.

Adhesive Interconnect Flip Chip Assembly

03/01/2005  The search for lead solder alternatives is stimulating interest in isotropic conductive adhesive assembly for flip chip interconnection.

Packaging Trends for the Next 10 Years

03/01/2005  Having been involved in the iNEMI roadmaps, recent workshops organized by the NNI, SRC and NSF, and discussions with semiconductor and packaging folk, it’s apparent that the semiconductor folks have figured out what’s going to happen in the next 10 years.

Influence of Design on Package Assembly

03/01/2005  Substrate design is largely driven by the performance requirements of a package and the fabrication limits of the supply chain.