Home » e-health » Tech Mahindra and ArisGlobal® partner for an end-to-end solution for Identification of Medicinal Products Compliance

Tech Mahindra and ArisGlobal® partner for an end-to-end solution for Identification of Medicinal Products Compliance

A positive step for the global Life Sciences Industry

Tech Mahindra Limited, a leading provider of IT, Networks & Engineering solutions and BPO services and ArisGlobal®, a leading provider of cloud-based software solutions for life sciences, have partnered to provide the life sciences industry with a complete end-to-end solution that will not only address the regulatory compliance requirement IDMP (Identification of Medicinal Products) brings, but also provide a solution which will enable companies to ensure compliance, improve efficiencies and assure the safety of their Tech Mahindra and ArisGlobal partnerproducts.

Wim Cypers, Senior Vice President at ArisGlobal stated “Life science companies currently focus on the upcoming EMA SPOR and future regulatory initiative but they also realize this is essential step but it is not the end goal for IDMP. It is clear that IDMP will impact other regulatory areas, not in the least in the area of patient safety and benefit/risk management. This partnership not only unites the regulatory and MDM expertise of both companies but also leverages our vast experience in other domains that will be impacted by IDMP. “

The solution provides both the technology as well as experience needed to provide companies with a clear path towards compliance and beyond. The IDMP solution helps companies to assess, collect and verify the information needed to achieve compliance through an application.

Venugopal Kandimalla, Global Head, Healthcare Life-Sciences Vertical – Tech Mahindra, commented “This engagement marks the coming together of two pioneering organisations and our alliance with ArisGlobal fosters mutual growth in regulatory space.”. This joint solution comprising of Master Data Management and regulatory interfacing application caters to EMA-IDMP compliance requirements of pharmaceutical companies.”


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