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Shruti Sharma

Product Specialist – Regulatory Services
Celegence

Shruti Sharma is an accomplished Product Specialist for CAPTIS, leveraging a strong background in Medical Writing to redefine the vision for technology products aimed at enhancing process efficiency in the life sciences regulatory space.

With over 7 years of expertise in Medical Device Regulatory Affairs, Shruti excels in Clinical Evaluations for Medical Devices across diverse therapeutic areas. Her proficiency extends to crafting essential regulatory documents, including CEPs and CERs, PMSRs, and SSCP, along with MDR compliant comprehensive CEP and CER templates for medical device manufacturers, tailored to the requirements of their product portfolio.

Shruti now plays a pivotal role in defining the direction for technology products within Celegence, where she seamlessly integrates her background in Medical Writing with cutting-edge technology solutions.

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