“विश्वकल्याण- शांतीदा। आरोग्यम् धनसम्पदा।”

Professional with good knowledge and experience in regulatory Affairs, clinical trial process, post-market compliance, complaint handling and vigilance activities.

 

Good Knowledge of Quality system for medical devices. (ISO 13485 Certified – Lead Auditor).

 

Experience in developing and executing regulatory strategy to facilitate launch of new products in key markets (India, Europe and Asia).

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