Pharmaceutical Technology EPR Monthly Issue:
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Pharm Tech
January 20, 2016
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PRODUCTION TRENDS

Pharmaceutical Manufacturers Go Green

Pharmaceutical companies reduce the impact of manufacturing on the environment with innovations in energy and waste treatment.
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Now Online

Crafting Standard Operating Procedures
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TROUBLESHOOTING

Advancing Container Closure Integrity Testing

The revised USP Chapter <1207> gives best practices for obtaining reliable data in container closure integrity testing.
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EXPERT INTERVIEW

Richard Johnson of the Parenteral Drug Association speaks with Pharmaceutical Technology about industry issues, including drug shortages.

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Packaging

Trends in Parenteral Fill–Finish

Automation and ready-to-fill packaging formats are expected to grow in parenteral fill–finish operations.
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Editor's Picks

Hygienic Safety Valve Protects Against Pressure Buildup

The Alfa Laval Safety Valve, a true spring-loaded safety valve, is designed to protect both equipment and people.
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System Monitors Temperature-Controlled Storage

The Infrastructure Monitoring System (IMS) 1000 from Sensaphone provides low-cost, 24/7 remote monitoring of unattended freezers and coolers used to store research material and pharmaceutical products.
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Metering Valve Incorporates COC Neck Gasket

The DF30Plus, a new version of Aptar Pharma's aerosol metering valve for pressurized metered dose inhalers (pMDIs), incorporates an elastomeric cyclic-olefin-copolymer (COC) neck gasket.
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Spectrophotometer System Automatically Handles Samples for Dissolution Testing

An ultraviolet light (UV) spectrophotometer system from Hanson Research automatically handles samples for pharmaceutical dissolution and diffusion testing.
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SPONSOR SHOWCASE

Tablet Press for Premum Large Batch Production

Fette Compacting America's FE75 Tablet Press is a double-sided rotary press that can be equipped with up to 115 punch stations to produce more than 1.6 million tablets per hour. Ideal for the premium production of large batches, the FE75's four compression rollers feature a special control system for direct compression, enabling the machine to operate with two intermediate pressures.
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Webcast

Controlling Contamination in Biopharmaceutical Manufacturing

On Demand

Experts review the sources of contamination, regulations and guidance documents on the control of potential contaminants in raw materials, and best practices to guard against the introduction of contaminants in the manufacturing process. The challenges of detecting contaminants, including mycoplasma, assay development, and testing practices are discussed.
Sponsored by: SGS Life Science Services

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EVENTS

IFPAC Annual Meeting

Jan. 24–27, 2016 | Washington, D.C.

PDA Annual Meeting

March 13–16, 2015 | San Antonio, TX

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eBOOK

Bioprocessing and Sterile Manufacturing eBook

Topics include aging facilities, cleanroom and facility planning, disposables, sterilization, lyophilization, and rapid sterility testing.

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