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DPIIT Recognition by StartUp India

Under the Startup India initiative, eligible companies can get recognised as Startups by DPIIT, in order to access a host of tax benefits, easier compliance, IPR fast-tracking & more. Learn more about eligibility and benefits below.

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ISO 27001:2013 Certification

ISO 27001:2013: ISO 27001 is the international standard that is recognized globally for managing risks to the security of information you hold. ISO 27001 describes the internationally accepted model for managing information security management systems (ISMS). This certification confirms our commitment to security, best-in-class service delivery, and validates the trust of our clients.

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Good Manufacturing Practice (GMP)

Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.

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Certificate of Compliance.

Certificate of Compliance is a document which certifies that the goods or services supplied meet the required standards. The document is a way of ensuring that consumers in the importing countries are protected against harmful or sub-standard products.

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ISO 9001 : 2015 Quality Management Services 

SO 9001 is the international standard for creating a Quality Management Systems (QMS), published by ISO (the International Organization for Standardization). The standard was most recently updated in 2015, and it is referred to as ISO 9001:2015. In order to be released and updated, ISO 9001 had to be agreed upon by a majority of member countries so that it would become an internationally recognized standard, which means it is accepted by a majority of countries worldwide.

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ISO 13485 : 2016 Quality Management System For Medial Devices 

The ISO 13485 standard is an effective solution to meet the comprehensive requirements for a QMS. Adopting ISO 13485 provides a practical foundation for manufacturers to address the regulations and responsibilities as well as demonstrating a commitment to the safety and quality of medical devices.