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 | EVENT | VENUE | LOCATION |
17-18 Mar 2020 | Outsourcing in Clinical Trials, Israel | International David Hotel | Tel Aviv, Israel |
6-7 May 2020 | Outsourcing in Clinical Trials, Europe | Espace Grande Arche | Paris, France |
27 May 2020 | Outsourcing in Clinical Trials, UK & Ireland | Royal Lancaster Hotel | London, UK |
20-21 Oct 2020 | Outsourcing in Clinical Trials, Nordics | Venue TBC | Copenhagen, Denmark |
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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
