3S Technologies - IT Computer System Validation Consulting Company
3S Technologies has an indepth insights into project/application validation, life cycle document development, change control implementation and 3rd party vendor auditing/qualification. Qualifying enterprise computer systems for 21CFRPart 210 & 211, (cGMP & 21CFRPart11 (ERES) & [EU GMP]-EudraLex-Rules governing medicinal products in the European Union–Volume 4–Guidelines to GMP for medicinal products for human use-Products for Human and Veterinary Use, Annex 11).
