Infotehna signs an agreement with Maneesh Pharmaceuticals Ltd

Infotehna is pleased to announce its further expansion into the new markets. Pharmaceutical company Maneesh Pharmaceuticals Ltd with its headquarters in India has engaged into the project of implementation of Infotehna's Electronic Document Management Solutions (EDMS) for Pharmaceutical Industry.

Infotehna's flagship solution SubmissionExpert™, including state-of-art eCTD publishing tool, will be implemented during next few months in Maneesh Pharmaceuticals and its UK joint venture Tillomed.

Infotehna’s SubmissionExpert™ - The RIGHT Choice

SubmissionExpert™ is a comprehensive solution that leverages Infotehna’s own compliance process control engine coupled with EMC/Documentum’s flagship content management technology. The solution delivers regulatory document control in accordance with cGMP and GAMP guidelines. In addition to its comprehensive document lifecycle workflow, cGMP change control, security model, audit trails, digital/electronic signature capability, version control PDF and eCTD, SubmissionExpert™ includes an integrated input/capture and publishing capability for document rendering, PDF and eCTD publishing, and eCTD XML generation. The system is fully compliant with 21 CFR Part 11 guidelines for closed systems and is validation ready. SubmissionExpert™ delivers a total solution for regulatory affairs organizations.

Over a period of two decades, "Maneesh" Pharmaceuticals has encountered a radical transformation. Due to excellent growing qualities and timely implementation of resources, this one-man initiative is now growing and multiplying across the globe. Today, Maneesh Pharmaceuticals is one of the very few companies which offer specialized manufacturing facilities dedicated to critical therapeutic segments. Besides this, Quality solutions in manufacturing, marketing and research play a key role in the rapid growth of the company.