Newsletter | January 22, 2013

01.22.13 -- Advanced Incubation Solution For Cell-Based Research

Laboratory Network.com Newsletter

Featured Article

Basics Of Labwasher Cleaning Validation
A Q&A with James Espiritu, Miele
Validation is vital to pharmaceutical processes because it assures quality, consistency, and keeps your operations compliant with GMPs. The FDA provides guidance for proper cleaning validation, however challenges occur because interpretation of those procedures vary between facilities.

Industry News

Advanced Incubation Solution For Cell-Based Research

Hamilton Robotics Safeguards Blood Transfers

PsiOxus Therapeutics Awarded $3.3M Contract To Develop Biodefence Vaccine Adjuvants

Pharma And Biotech Firms Trust CompacT Automated Cell Culture To Generate Cell Lines

Eppendorf Introduces New Rotors For Centrifuges 5804/5804 R And 5810/5810 R

Even More Flexibility With New Combi-Block For Techne Prime Thermal Cyclers

Labcyte Launches First Large-Volume Acoustic Liquid Handler

Novel Platform Combining A Plate Reader With An Imaging Cytometer Developed

Akonni Biosystems Expands Family Of TruTip Extraction Products For Hamilton Microlab STAR Line

LifeLabs Medical Laboratory Services Agrees To Purchase B.C. Biomedical Laboratories
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Featured Downloads

Reinventing Drug Titration For IC50 Determinations
Tecan and HP have teamed up to reinvent the drug titration process for small molecules by providing a solution which eliminates the traditional serial dilution process, going from concept to experiment to results much faster and giving access to compound studies that were previously impractical. 

FS209E And ISO Cleanroom Standards: White Paper
Before global cleanroom classifications and standards were adopted by the ISO, the U.S. General Service Administration's standards were applied virtually worldwide. However, as the need for international standards grew, the ISO established a technical committee and several working groups to delineate its own set of standards.

A 15-Minute Guide To Compliant Document Management
Life Sciences quality and manufacturing organizations face three critical industry forces: increasingly stringent regulation, globalization, and virtualization of supply networks.
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