Articles by Paul Smith - Pharmaceutical Technology

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Articles by Paul Smith

Paul Smith


Paul Smith is EMEAI laboratory compliance productivity specialist at Agilent Technologies UK Ltd, 610 Wharefedale Road, IQ Winnersh, Wokingham, Berkshire RG41 5TP, United Kingdom, paul_smith@agilent.com

Articles
Data Integrity in the Analytical Laboratory
May 2, 2014

Data integrity in the analytical laboratory is an area of increasing focus for regulators such as FDA.

FT-IR Identification: the Expertise Required To Ensure Compliance
September 1, 2011

By providing an information "fingerprint", infrared red spectroscopy is a useful tool for identifying counterfeit pharmaceuticals. The authors identify best practices for ensuring compliance.

Use Of RFID Asset Management Systems For Monitoring Analytical Instrumentation
September 1, 2010

Utilizing integrated active radio frequency identification (RFID) and real-time asset management systems can yield commercial and compliance benefits.

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FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
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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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