Provide systematic approach for Handling of Deviation Management (Unplanned deviation, OOS, OOT, Market complaints change controls and CAPA).
Provide Quality product life cycle approach implementation and evaluation of products scientifically.
Quality matric implementation at Mfg. site level.
Provide an opportunity to each problem to build robust quality system with scientifically.
Offer sound investigation team to conduct throughout investigation for provide elimination with replacement. Facilitation cost effect CAPA to prevent re-occurrence of issue.
Documentation- preparation of various SOPs, Protocol, BMRs.
Provide stability studies approaches for various countries for API, Formulations.