For standard analytical methods (also referred to as compendial methods) described in the Pharm. EU it is not required to validate every parameter. Depending on the category of the method (I-V) the method needs no verification at all or verification of certain parameters assuring their suitability under actual conditions for their intended use. However, because such method descriptions tend to be not very detailed, experience and a strong scientific background is required to actually perform these methods appropriately.
VelaLabs is capable to perform most of these compendial methods - either by itself or in collaboration with trusted, audited and GMP-certified subcontractors.