Articles by Michelle Perez - Pharmaceutical Technology

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Articles by Michelle Perez

Michelle Perez


is a manager of global regulatory consulting operations at ISI, which has offices in North America, Europe, and Adia.

The eCTD Upgrade: Cross-Application Linking
February 2, 2010

How to cut time and cost by re-using already submitted documents.

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FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
Reducing drug shortages
Breakthrough designations
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Expedited reviews of drug submissions
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Reducing drug shortages
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Breakthrough designations
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Protecting the supply chain
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Expedited reviews of drug submissions
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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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