Regular testing of balances and scales is the only way to uncover malfunctions early and help eliminate inaccuracies that might otherwise go undetected until the next service calibration. More and more people realize that it is both less pricey and more… Read More
Blog
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Weighing for Pharmaceutical Manufacturing: Liquid Medicine
Different installation heights, compliance with some hygienic design directives, total weighing reliability, and other reproducible weighing solution results presented a challenging task for the plant manufacturer Pharmatec. If you’d like to learn more about weighing for pharmaceutical manufacturing with liquid medicine,… Read More
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IQOQ White Paper
In the highly-regulated pharmaceutical, clinical, and medical industries, even minor inconsistencies can become severe problems without the correct qualification and validation protocols set in place. As a quality assurance component, equipment validation is crucial for producing consistent, high-quality products. One… Read More
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Equipment Records for GLP Audits
There is a lot that goes into keeping equipment records for GLP audits. They are broken down by topic, relevance to the FDA, EPA, and the equipment used. You’ve come to the right place for information about different equipment records for… Read More
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Pipette 101: Reverse Pipetting
Reverse pipetting is aspirating a bit extra to dispense the proper amount. Reverse pipetting is handy while pipetting viscous, foaming, and high vapor pressure or other low surface tension liquids. The technique is mainly recommended for solutions with high viscosity or a… Read More
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Monitoring Sterility during Drug Development
While inactivated or live attenuated vaccines usually dominate the market, a newer generation of viral vaccines known as recombinant viral vectors, or VLPs (virus-like-particles, are in the pre-clinical and clinical development phases. Viral vectors are widely used for gene therapy… Read More
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Our A2LA Accreditation
We have been granted an accreditation certificate in recognition of the successful completion of our A2LA evaluation process. We have maintained our ISO 17025 Accreditation since 1990, formerly known as Guide 25. In today’s article, we will break down some of the data included… Read More
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History of Sterility Testing
Way back in 1927, Sartorius manufactured membrane filters which for the very first time made the sterilization of heat-sensitive solutions entirely possible. These membranes have now been continually enhanced for a wide range of applications and remain at the core… Read More