Equipment and Processing Report, Nov 21, 2012 - Pharmaceutical Technology

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Equipment and Processing Report, Nov 21, 2012
Production Lines
Protecting the Public: Anticounterfeiting
By Hallie Forcinio
Overt and covert packaging technologies have evolved to authenticate drugs and fight counterfeits.
In the Mixer
Designing a Clean-in-Place System
By Andrew Wong , Cody Shrader
An efficient cleaning cycle begins with equipment and automation-system design.
Troubleshooting
Using As-Found Data in a Pipette Calibration Program
As-found data is a crucial component of pipette calibration for laboratories that must comply with GMP regulations.
Editor's Picks
November 2012 Editor's Picks: Products from Malvern Instruments and GEA Pharma Systems
Products from Malvern Instruments and GEA Pharma Systems

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Survey
FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
Reducing drug shortages
Breakthrough designations
Protecting the supply chain
Expedited reviews of drug submissions
More stakeholder involvement
Reducing drug shortages
33%
Breakthrough designations
11%
Protecting the supply chain
39%
Expedited reviews of drug submissions
11%
More stakeholder involvement
6%
View Results
Jim Miller Outsourcing Outlook Jim Miller Health Systems Raise the Bar on Reimbursing New Drugs
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerThe Mainstreaming of Continuous Flow API Synthesis
Jill Wechsler Regulatory Watch Jill Wechsler Industry Seeks Clearer Standards for Track and Trace
Siegfried Schmitt Ask the Expert Siegfried SchmittData Integrity
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