OpenText Quality and Manufacturing

Ideal for	Built to
Pharmaceutical Companies Contract Manufacturing Organizations Drug Manufacturing Operations	Achieve compliance with GMP standards Improve productivity across the extended enterprise Increase efficiency with streamlined, automated workflows

Benefits

The OpenText Quality and Manufacturing solution enables life sciences organizations to control quality and manufacturing documents, automate workflows across the extended enterprise, and ensure complete compliance with Good Manufacturing Processes (GMP).

COMPLETE COMPLIANCE
Achieve compliance with GMP standards through enhanced, automated management of standard operating procedures and process control documents.

CENTRALIZED CONTROL
Centralize corporate document control and visibility, while enhancing local productivity with a solution that unifies document creation, approval, change control, and retrieval, and also provides flexibility in workflows and document lifecycles.

SECURE MOBILE COLLABORATION
Seamless integrations with mobile devices allow easy distribution of effective documents, enable secure synch and share across devices, and the ability to participate in workflows on the go.

LOWER COSTS WITH OpenText ONDEMAND
Eliminate IT infrastructure expenses and delays in acquiring hardware and installing software with OpenText OnDemand, a private cloud-based, managed service. Take advantage of the highly secure and compliant architecture with global access.