Consultancy services for MedTech firms in the realm of Quality Management, Clinical Investigation Management, Regulatory & Information security/ Privacy. Implementation of standards like ISO 13485, IEC 82304, IEC 62304, ISO 14971, IEC 62366 etc aligned to medical device regulations. Core offerings include QMS process/procedure definition, deployment facilitation and training. Allied activities include Privacy & Information Security standards implementation eg: ISO 27701, ISO 27001 for medical device products. End to end clinical investigation management for safety and clinical efficacy of medical devices is another key offering. Sustainability and related environmental friendly design inputs for medical devices are in built in the processes defined for our clients.