Pacific BioLabs has purchased a new Sciex Triple Quad 6500+ LC-MS/MS. This instrument is a great addition to our existing AB Sciex API 4000 QTrap LC-MS/MS and Sciex 5600 Triple TOF-MS. It will be primarily used for quantitative bioanalysis of small and large molecules. This instrument relies on the IonDrive Technology that provides high sensitivity, […]
Pacific BioLabs is proud to announce successful accreditation for ISO 17025:2017, General Requirements for the Competence of Testing and Calibration Laboratories, through the ANSI-ASQ National Accreditation Board. PBL’s accreditation for ISO 17025:2017 replaces PBL’s past certifications for ISO 9001:2008 and ISO 13485:2003 and is considered more appropriate for a CRO. The scope for PBL’s 17025 […]
For their March issue, Medical Product Outsourcing Magazine interviewed Ryan Harper, PBL’s Business Development Director, regarding recent medical device testing changes and developments. The article discusses current industry trends, additions to ISO 10993, performing risk assessments as well as new technologies and approaches. The MPO article can be accessed here.
Trade Shows and Events
Pacific BioLabs will attend and exhibit at PBSS-SF Bay Area’s workshop on regulated bioanalysis (RBA). It is required in key parts of drug development that involve evaluations of drug safety, bioequivalence, and pharmacokinetics, and RBA data quality directly impacts the reliability of such assessments. RBA Method Validation requires compliance with various national method validation guidances, […]
PBL will be a proud exhibitor at the Cleaning Validation summit in October. It will feature lessons learned and case studies from industry experts and comprehensively cover: Understanding the 2018 FDA Guidance on Regulatory Submissions for Cleaning Validation Current Best Practices for Regulatory Audits of Cleaning and Cleaning Validation Practices ASTM Standards in Medical Device […]
The AAPS PharmSci 360 attracts pharmaceutical scientists who work across all stages of drug development including discovery, development and manufacture of pharmaceutical products and therapies. The sessions span preclinical development, clinical pharmacology, manufacturing and bioprocessing, formulation and quality.
Pacific BioLabs is proud to be an exhibitor at the E&L conference. This two-day conference will examine the safety, quality, and regulatory issues involved in a wide array of contexts central to the pharmaceutical and biotech industries, including drug packaging and delivery components, single-use systems, medical devices, and parenteral drug products. In addition, this conference […]
Back for its 11th year, BIOMEDevice San Jose brings together more than 1,500 medical device industry professionals and 250+ suppliers on one floor for this premiere, must-attend event. Join other industry leaders and experts from across Silicon Valley’s booming medical device design and manufacturing community to learn more about the latest developments, trends, and technological breakthroughs across […]