The Service Leader in Bioscience Testing

Good service means doing it right the first time, on time.

​Bin Z., Bioanalytical Director


Breadth of Management Experience

PBL senior managers are highly qualified, knowledgeable, experienced and focused.

Mike Y., Executive Vice President


Employees are the Most Important Resource

The work can be challenging but I have learned so much and I know my efforts are appreciated.

Shaiela B., Client Account Manager


Robust Quality Systems

Outstanding regulatory compliance is the backbone of PBL.

Thomas C., Associate Vice President, Quality Assurance


Built on a Solid Foundation

Our facility is purpose built with cGMP and GLP compliance in mind.

Tom Spalding, President


Established in 1972

Mart Spalding Sr. started PBL to provide an unmet need in the science community.

Tom Spalding, President


Pharm/Biopharm Manufacturing Support

Pharm/Biopharm Manufacturing Support

Small and Large Molecule Manufacturing Support.

Pharm/Biopharm Manufacturing Support

Pharm/Biopharm Development Testing

Small and Large Molecule Development Support.

Pharm/Biopharm Manufacturing Support

Clinical Trial Support

Immunogenicity and Bioanalysis for Clinical Trials.

Pharm/Biopharm Manufacturing Support

Medical Device Tests

Medical Device, Delivery Device, and Combination Product Services.


The Power of My PBL

Access your reports, study and submission status, invoices, quotes and purchase order information all at one secure location on the web.



September 30, 2019

PBL Purchases Sciex Triple Quad 6500 Plus LC-MS/MS

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, […]

March 27, 2019

PBL Is Now ISO 17025:2017 Accredited

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 […]

March 26, 2019

Pacific BioLabs featured in MPO’s article – Transformative Testing: Addressing Patient Safety and Cybersecurity

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

October 3, 2019 | Foster City, CA

PBSS Small-Molecule Bioanalytical Method Validation & Regulated Bioanalysis: Fundamentals, the New FDA Guidance and Regulatory Trends

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, […]

October 9-10, 2019 | La Jolla, CA

Cleaning Validation Summit 2019

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 […]

November 3-6, 2019 | San Antonio, TX

PharmaSci AAPS 360

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.  

November 18-19, 2019 | La Jolla, CA

Extractables & Leachables Forum 2019 – West Coast

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 […]

December 4-5, 2019 | San Jose, CA

BIOMEDevice 2019

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 […]

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