News & Events
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December 7, 2010
New White Paper Examines Clinical Trial Material Production & Testing: What Your Contract Manufacturing Organization is Not Telling You
November 16, 2010
New White Paper: Having a Solid Package Validation Program Can Prevent Failure of Combination Products
November 5, 2010
Combination Products
Manufacturing Website Launch
October 5, 2010
USP Microbial Examination of Non-Sterile Products: New White Paper is Roadmap of Regulations for Manufacturers
June 2, 2010
New White Paper Helps Medical Device Manufacturers Validate Cleaning Processes
May 29, 2010
“Get with the Program -- Having a solid package validation program can prevent failure of combination products” by Steven Richter is a featured article in Medical Device & Diagnostic Industry’s May 2010 issue:
http://www.mddionline.com/article/testing-validation
FDA concerns regarding terminally sterilized medical products are based on years of data that implicate failures in primary packaging. Approximately 47% of failures occur due to inadequate package validation programs. This article provides insight into the general requirements in a microbiological and physical testing program. It discusses how combination products pose a unique set of challenges to package validation engineers.
May 3, 2010
“Information Transfer
for Early Stage Fill/Finish Clinical Trial Material" Presentation
is Featured at BIO International Convention
May 3, 2010
Microtest Labs Provides
Complete Fill and Finish Manufacturing Services for Clinical Trial
Material
April 21, 2010
New, Free White Paper:
“Environmental Monitoring and Certification in Controlled
Environments: Meeting Regulations and Achieving Effective Microbial
Control for Pharmaceutical and Medical Device Manufacturers”
April 21, 2010
Microtest Labs Provides
Experienced USP Microbial Limits Testing of Raw Materials, Other
Nonsterile Products for Pharma Manufacturers
April 21, 2010
Microtest Labs Offers
Expanded Clean Room, Contamination Testing Services for Medical
Device Manufacturers
April 21, 2010
Microtest Labs is
a Leader in Cleaning Validation Studies for Medical Devices Designed
for Reuse
April 20, 2010
White Paper Explains
Aspects of Testing >From Purified Bulk Drug Substance to Sterile
Liquid Final Drug Product
April 20, 2010
Microtest Labs Provides
Experienced USP Microbial Limits Testing of Raw Materials, Other
Nonsterile Products for Pharma Manufacturers
April 5, 2010
New White Paper for
Dietary Supplement Manufacturers Provides “How-to”
for New “Compliance Paradigm”
January 19, 2010
New White Paper Examines Advanced Mycoplasma Tests - How Real-Time PCR Analysis Helps Save Time and Money for Biopharmaceutical Manufacturers
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