New White Paper Details What Compounding Pharmacies Must Know to Prepare for FDA Inspections
4/16/2013 11:22:55 AM
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MicroTest Laboratories: Disinfectant Qualification Questions are Answered for Sterile Drug Manufacturers in New White Paper
3/20/2013 11:37:22 AM
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MicroTest Laboratories Release: New White Paper Assists Medical Device Manufacturers With Changes to FDA Endotoxin Testing Guidelines
10/25/2012 9:46:16 AM
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New Scope of Reusable Medical Device Cleaning Validations is Examined in New White Paper From MicroTest Laboratories
10/4/2012 12:20:57 PM
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MicroTest Laboratories Release: Boston Seminar to Assist Medical Device & Pharmaceutical Manufacturers With Environmental Monitoring, Risk-Assessment
9/25/2012 10:59:05 AM
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Use Notebook Studies to Ensure Successful Reusable Device Cleaning Validations, Recommends MicroTest Laboratories
8/15/2012 10:30:00 AM
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MicroTest Laboratories Release: Six Critical Areas to Ensure Regulatory Compliance in Aseptic Manufacturing are Outlined in New Management Brief
7/31/2012 11:32:45 AM
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MicroTest Laboratories Release: Clean Room Environmental Best Practices for Medical Device & Pharmaceutical Manufacturers are Focus of Boston Seminar on June 6
5/30/2012 11:47:47 AM
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MicroTest Laboratories: Pharmaceutical Consultants are Focus of May 16th Conference in Boston
5/2/2012 10:51:31 AM
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MicroTest Laboratories Release: Industry Perspective on Reusable Medical Device Cleaning and Validation Requirements Outlined in New Management Brief
5/1/2012 9:54:49 AM
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