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
70%
Breakthrough designations
4%
Protecting the supply chain
17%
Expedited reviews of drug submissions
2%
More stakeholder involvement
7%
View Results
Eric Langerr Outsourcing Outlook Eric LangerTargeting Different Off-Shore Destinations
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerAsymmetric Synthesis Continues to Advance
Jill Wechsler Regulatory Watch Jill Wechsler Data Integrity Key to GMP Compliance
Sean Milmo European Regulatory WatchSean MilmoExtending the Scope of Pharmacovigilance Comes at a Price
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