Designed to focus on creating paperless environment and employees to
manage their documents remotely and securely
Strict standards regulate product development activities of pharmaceutical companies from the preclinical stage through to the post-market stage. Specific conformance requirements on SOPs, compliances like GCP, GLP, and CGMP mark the processes. In the course of operations, voluminous amounts of data meant for processing is generated. From a compliance point of view maintaining data security and accuracy of data is critical. Addressing concerns, an effective document control and management system is crucial to ensure documents are preserved traceable, retrievable, revisable and approvable when needed.
Motto Systems, a proven player in the area of quality management systems, shows how software solutions can leverage processes and resolve challenges of document control and management. Built in accordance to the highest DMS compliant procedures, our solution comes with an end-to-end set of features spanning the whole document life cycle from pre-clinical to post-clinical phase to submission and archiving of regulatory documents.
Motto Systems process and document management software provide a solid foundation for effective document control making compliance easier and quick. Our solution promotes the efficiency of workflow and takes collaborative actions of the company to the next level.