Meet the Intertek team during the Outsourcing in Clinical Trials Conference Series, and discover how experts at our GCP accredited laboratories can support your PK/PD, immunogenicity or biomarker studies.

Intertek has over 20 years experience in conducting regulated bioanalytical studies supporting the development of pharmaceuticals, biopharmaceuticals, vaccines and biosimilars. Expert bioanalysis support for both small molecule drugs and biologics is provided through our global network of state-of-the-art, GLP-compliant laboratories and capabilities include proprietary method development, validation, method transfer, high throughput sample analysis and pharmacokinetic and toxicokinetic support, combined with automated data capture and reporting system.

 

Contact our Bioanalysis Team now to arrange a meeting at any of these events. 

 

DATE    EVENTVENUELOCATION
17-18 Mar 2020Outsourcing in Clinical Trials, IsraelInternational David HotelTel Aviv, Israel
6-7 May 2020Outsourcing in Clinical Trials, EuropeEspace Grande ArcheParis, France
27 May 2020Outsourcing in Clinical Trials, UK & Ireland Royal Lancaster HotelLondon, UK
20-21 Oct 2020Outsourcing in Clinical Trials, NordicsVenue TBCCopenhagen, Denmark

   

Learn More 

Recognizing the critical role bioanalysis plays in drug development, our mission is to consistently deliver accurate and reliable data that is subject to rigorous scientific and regulatory review, ensuring the success of your discovery, preclinical and clinical programs.

 

BROCHURE: Intertek Bioanalysis Services

WHITEPAPER: Bioanalytical Quantitative Determination Of Pegylated Species In Human Plasma By NMR

WHITEPAPER: Technologies to Measure Immunogenicity

FACTSHEET: Biomarker Development and Validation

 

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