About Us
Adwith is a specialized medical device regulatory consulting company that supports healthcare manufacturers in navigating complex regulatory landscapes and achieving successful market entry across global markets.
We provide comprehensive turnkey solutions that guide manufacturers through every stage of their journey — from product design and development to manufacturing facility planning and regulatory approvals at both national and international levels.
Our services are designed to help medical device companies meet regulatory requirements efficiently while maintaining the highest standards of quality and compliance.
Our Vision
Our vision is to become a global leader in medical device regulatory consulting and turnkey project solutions, delivering comprehensive expertise from concept to compliance. We strive to set the benchmark for excellence by providing strategic guidance, innovative solutions, and uncompromising quality to healthcare manufacturers worldwide.
Our Mission
To deliver a comprehensive range of high-quality services at affordable costs by leveraging advanced technology and cloud-based platforms. We aim to build long-term relationships with our customers by ensuring trust, maintaining the highest standards of quality, and providing reliable and timely services.
Our Core Services
Our core services include regulatory strategy and advisory, product design and development guidance, and support for manufacturing unit design and setup. We assist companies in obtaining necessary licensing and regulatory approvals, implementing Quality Management Systems (QMS), and managing certifications and compliance documentation. We work with start-ups, emerging innovators, and established medical device manufacturers, providing customized consulting solutions tailored to their specific needs. Our experienced regulatory specialists help organizations develop safe, effective, and compliant medical devices that meet national and international regulatory standards.
International Regulatory Support
Adwith provides regulatory consulting services for multiple international markets, including: Costa Rica, United Kingdom, Oman, South Africa, Saudi Arabia, United States, Egypt, Brazil, Germany, and the Netherlands. With a focus on cost-effective services, timely project delivery, and regulatory excellence, Adwith helps healthcare companies expand their operations globally with confidence. Get expert regulatory guidance today. Contact us for a free consultation.
Our Founder and CEO
Adwith is built with a simple idea to make certifications like ISO easy, clear, and stress free for every business. Instead of complicated processes, it focuses on guiding organizations step by step, helping them meet required standards and build strong credibility without confusion or delays.
With a practical and reliable approach, Adwith provides complete certification support tailored to real business needs. From documentation to final approval, everything is handled smoothly to ensure quick results, better compliance, and long-term trust helping businesses grow with confidence and a stronger market presence.
The visionary founder of Adwith is driven by a passion for transforming how brands grow in the digital space. With a strong focus on creativity, strategy, and innovation, Adwith has been built as a platform that helps businesses establish a powerful online presence and connect meaningfully with their audience.
Under this leadership, Adwith delivers result-oriented digital marketing solutions tailored to modern business needs. The approach combines data driven strategies with creative execution to ensure sustainable growth, stronger brand identity, and long-term success for every client.
Dr. Sadhna Gaur
Our Core Team
Sumit Singh
Senior Consultant (ISO Standards, BIS, CE, USFDA)
Avinash Bhardwaj
Senior Consultant (ISO Standards, CDSCO Regulatory)
Harshit Sharma
Consultant (ISO Standards, CDSCO Regulatory)
Reet Sharma
Consultant (Legal Compliance)