About Avinash MedTech Solution
Avinash MedTech Solution is a specialized regulatory and quality consultancy firm established in 2024, dedicated to supporting medical device manufacturers, importers, and healthcare organizations in achieving compliance with national and international standards.
We provide end-to-end consultancy services for CDSCO registration, ISO certifications (ISO 13485, ISO 9001, ISO 14971), CE marking, BIS certification, and ZED certification. Our focus is to simplify complex regulatory processes and help businesses bring safe, compliant, and high-quality medical products to market efficiently.
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Our Expertise
With deep knowledge of regulatory frameworks and quality management systems, we assist organizations at every stage—from product classification and documentation to submission, approval, and certification.
Founded by Avinash Sharma, a certified ISO 13485 Lead Auditor, our firm combines practical industry experience with a result-oriented approach. We not only help clients achieve certifications but also build sustainable compliance systems for long-term success.
Our Vision
To become a trusted global partner in medical device regulatory and quality consulting, empowering organizations to achieve excellence in compliance, safety, and innovation.
Our Mission
- To provide reliable and transparent consultancy services
- To simplify CDSCO and international regulatory processes
- To implement strong Quality Management Systems
- To ensure faster market access through efficient compliance
- To build long-term, value-driven client relationships