02.04.2010 -- Today's Issues Of Containment For Solid Dosage Production

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Today's Issues Of Containment For Solid Dosage Production
By GEA Process Engineering Inc.
When talking today about solid dosage form production, in 9 out of 10 cases containment immediately becomes one of the issues. Why? The first reason is that APIs are becoming more and more potent. The second reason is that health and safety authorities all around the world are putting more focus on the protection of operators dealing with these substances. The third reason is that suppliers of various hardware components have developed a huge variety of containment solutions.

The Use Of Syringe Filters For Analytical Sample Preparation
By Larry Scheer, Pall Life Sciences
Filtration is increasingly used as a protective measure in analytical sample preparation. As a result, there are more filter options to choose from than ever before, and each has its own performance properties.

Noninvasive Delivery Offers Opportunities For Large And Small Pharma
By Edward Maggio, Ph.D., Life Science Leader magazine
Peptide and protein drugs are among the most useful and effective drugs yet discovered, exhibiting potent biological activity, high binding specificity for specific biological targets, and essentially no chemical toxicity with few or no drug interactions. There are more than 140 peptide and protein drugs in current use today, and their number and importance is rapidly increasing.

The Synthesis Of 3-Methyl Salicylic Acid [ring-14C(U)]
By Analytical Bio-Chemistry Laboratories (ABC Labs)
3-Methyl salicylic acid is an important precursor for the synthesis of many biologically active species. For example, Moreau reported the synthesis of a series of aryhydrazones and evaluated their vitro antifungal properties against two human pathogenic yeasts.

The Business Benefits Of Calibration
By Beamex
Calibration can be briefly described as an activity where the instrument being tested is compared to a known reference value. At the simplest level, calibration is a comparison between measurements — one of known magnitude or correctness made or set with one device — and another measurement made in as similar a way as possible with a second device.

Speical Report: Filtration

White Paper: PAT Initiatives And TOC Measurements For Higher Product Quality And Profitability
In recent months, the use of PAT (Process Analytical Technology) terminology has consumed the vocabulary of pharmaceutical professionals. At its core, the PAT initiative is designed to address manufacturing-related quality issues in the pharmaceutical industry by encouraging process innovation.

Brochure: Niro Model M Membrane Filtration Pilot Plant
The GEA Filtration Model M Pilot Plant is a laboratory-scale test plant designed for feasibility testing of cross-flow membrane filtration applications in the microfiltration, ultrafiltration, and nanofiltration ranges.

Brochure: Finn-Aqua BPS Biopharmaceutical Steam Sterilizer (Autoclave)
Finn-Aqua GMP Steam Sterilizers provide shortened validation, increased reliability, and flexibility. Each sterilizer is available with all the standard sterilization processes that utilize steam as the sterilizing agent, including saturated steam, steam-air mix and water-air mix. Customized cycles can also be developed, based on customer-specified requirements.

INTERPHEX Puerto Rico Booth 808

Datasheet: Sartobran® P 0.1 µm Sterilizing Grade Filter Cartridges
Sartobran P 0.1 µm rated, high-flow filter elements are designed to give enhanced sterility assurance for applications with microorganisms present that can pass through 0.2 µm rated sterilizing grade filters.

Brochure: FiberFlo Teflon Pleated Cartridge Filters
Containing 8.0 square feet of expanded PTFE membrane, FiberFlo Teflon Filters offer users a highly efficient hydrophobic "barrier", ensuring low moisture content of ultrapure gasses. Additionally, it will ensure filtration performance in the purification of aggressive liquids and organic solvents.

White Paper: The Need For A Broader Perspective If PAT Implementation Is To Be Successful In The Pharmaceutical Sector
Process analytical technology (PAT) has the potential to deliver significant shifts in the economics of the pharmaceutical sector. In the years since the FDA published its guidance on PAT, there has been a wealth of research and comment articles on its adoption by the industry.

Datasheet: Tangential Flow Filtration Systems
Pall offers scalable, predesigned systems to suit your specific process needs. Pall Standard systems are ready-to-use, engineered systems with integrated recipe management tools to expedite your approval processes and reduce your time to market.

Datasheet: Liqui-Flux W03 Water Filtration Product
Liqui-Flux modules are designed to filter surface, brackish, potable, municipal, process water, and water feeding RO desalination systems.

Guide: Laboratory Water Purification
Provides an overview to laboratory water purification including water quality standards, contaminants, and purification methods. A glossary of terms is included.

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