Document Management System

Challenges like lack of proper document escalation flow, improper document revision and getting document signatures made AmpleLogic to design and develop Electronic document management system. In Pharmaceutical companies each and every activity within a GMP regulated environment such as US FDA, MHRA is based upon controlled documents and revision control. Therefore Document Control, Management and Issuance is core to the functioning of the Life Sciences companies and exhibiting Compliance and Quality. AmpleLogic improves document access, achieve assured regulatory compliance and resolve all the major challenges related to Document Management.AmpleLogic DMS features include search, separate work flow for every document type, numbering, document comparison, auto supersede and many more