Certification Services

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ISO 13485 is an internationally recognized standard specifically designed for Quality Management Systems (QMS) in the medical device industry. It provides a framework for organizations involved in the design, production, installation, servicing, and distribution of medical devices to ensure their products consistently meet customer and regulatory requirements. The current version, ISO 13485:2016, came into effect in March 2016.

Approx. Rs 5,500 / CertificateGet Latest Price

An FDA certification sample, in the context of food, drugs, and medical devices, usually refers to a sample of a product or batch submitted to the FDA for analysis to ensure it meets regulatory standards. It can also refer to certificates issued by the FDA for products like food and food contact substances, dietary supplements, medical devices, and drugs. These certificates demonstrate compliance with FDA regulations and may be required for export or other purposes

Approx. Rs 5,000 / CertificateGet Latest Price

WHO-GMP (World Health Organization Good Manufacturing Practice) certification is a globally recognized standard that ensures pharmaceutical companies maintain high-quality production standards for their medicines. It verifies that a company's manufacturing processes adhere to WHO guidelines, ensuring product safety, efficacy, and quality. The certification covers various aspects of the manufacturing process, including facilities, equipment, documentation, and quality control systems.