FEATURED LABORATORY ARTICLES & APPLICATIONS

  • 10 Basics To Achieving Labwasher Cleaning Validation

    For pharmaceutical processes, validation is key as it assures consistency, quality, and keeps operations compliant with the FDA’s Current Good Manufacturing Practice regulations, or cGMP. While the FDA provides proper cleaning validation guidance, challenges occur as interpretation of those procedures may vary between facilities.

  • Remote SDV/SDR: Alternatives To Redact/Fax

    As part of their risk-based monitoring strategy, many sponsors and CROs are using remote techniques to conduct source data review and verification (SDR and SDV).The best implementations out there actually streamline activities at both ends, both for sponsors/CROs and for study sites.

  • Optimizing Methods In Microtissue Cultivation

    Cells grown in standard suspension or monolayer culture lose many features that are characteristic of cells in tissues and limit their use to study certain aspects of cell biology.

  • A New Approach To Laboratory Efficiency: On-site Instrument Concierge Service

    Scientists are spending an enormous amount of their time and effort simply getting instrumentation to the point that it can be used,” the NRC reports. “This wasted time can be used more productively when a well-functioning repair and maintenance system is in place.

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LATEST NEWS

  • Sevion Therapeutics Announces Establishment Of A Biophysical Characterization Applications Lab

    Sevion Therapeutics, Inc. (“Sevion” or the “Company”), a biopharmaceutical company which discovers, develops and acquires next-generation biologics for the treatment of cancer and immunological diseases, has entered into an agreement with Malvern Instruments establishing a new biopharmaceutical applications laboratory in the heart of San Diego’s biotechnology cluster

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INDUSTRY EVENTS

Project Management: Best Practices for Validation & Regulatory Projects

August 5, 2015
1pm-2:30pm EDT, Online Training

Cloud Computing In A GxP Environment: Three Key Success Factors

August 13, 2015
1pm-2:30pm EDT, Online Training

21 CFR Part 11: Understanding the ERES Regulation for Compliance Success

August 25, 2015
1pm-2:30pm EDT, Online Training

Cleaning Validation – Lessons Learned in the Trenches

August 26, 2015
1pm-2:30pm EDT, Online Training
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