When do you need method development or validation?

Bureau Veritas provides method development and validation services for a wide variety of compounds for which sampling and analysis protocols are not available.  The service is applicable for active pharmaceutical ingredients (APIs), proprietary chemicals, industrial chemicals and intermediates, nanomaterials, as well as products in the client development pipeline.  Bureau Veritas also offers industrial hygiene analytical method development and validation services specific for surface and air sampling.

The Bureau Veritas industrial hygiene laboratory offers the most advanced instrumentation technologies and more than 80 professional staff, including certified industrial hygienists (CIH), chemists (Ph.D., MS, and BS levels), and microscopists. We have developed more than 500 sampling and analytical methods over the last two decades.

While many of the methods are proprietary, some have been published in peer-reviewed journals, such as the Journal of Occupational and Environmental Hygiene (JOEH) and Journal of Oncology Pharmacy Practice. Our methods are developed in accordance with guidelines from OSHA, NIOSH, and US EPA.  We can also meet client requirements for US or international product registration support. 

Following the applicable guidelines, protocols can be customized to meet your project validation requirements. We also provide validation services on existing methods including method transfer, verification and storage stability. Our experts can remediate existing methods to bring those techniques up to current practices.