Method Development and Validation

In addition to the extensive portfolio of established methods available, Arista Laboratories has considerable experience in the development and validation of new methods and the transfer of existing methods.

Arista validates analytical methods in accordance with established international protocols, including those produced by ISO, ICH and FDA. In all cases the main objective of validation is to ensure that the developed method is fit for its intended purpose. Arista works closely with the client at all stages of method development to ensure that their needs are met.

Validation of an analytical method typically consists of a multi-day process where many facets of a method are evaluated including:  linearity and goodness of fit; limit of detection and quantitation; accuracy and precision; selectivity; extraction efficiency; trapping efficiency (for smoke emission methods) and stability.

Contract method development in all areas of expertise is available. A specific work plan is developed between the principal investigator and Arista. Commercial terms are negotiated on a case-by-case basis.