Experienced analytical chemists at iuvo can provide customized HPLC and GC method development for chromatographic assays supporting medical device or pharmaceutical R&D programs. With new method development, we work closely with our customers and the Quality Assurance Department to tailor methods and procedures that meet the specific needs of our customers. Methods can be validated and run routinely by our staff or we can collaborate with our customers to transfer methods. Routine testing performed by our staff is performed on qualified and calibrated instrumentation using controlled procedures to provide our customers with reliable results in a timely fashion.
Method validation services are also available to demonstrate method capability and performance. Method validation conducted at iuvo is compliant with pertinent USP, ICH, and FDA guidelines.v