Grow your business with us!About MedReg Consultancy
MedReg Consultancy was founded with one aim in mind – to empower medical device manufacturers by providing regulatory solutions. Since 2011, Medreg has served numerous clients across India, Europe, the USA, and the UK. We have helped medical device industries in obtaining various certifications and licenses, such as CE Certification, UK MDR, ISO 13485:2016 Certification, ICMED, MDSAP, USFDA Listing, Country Registration, UL Certification, USFDA 510K, CDSCO licenses MD-05, MD-06, MD-09, MD-10, MD-15, Free Sale Certificates, PMA, and various country registrations.
No matter the size of your business, our team of experts with deep industry knowledge will provide you with the knowledge, guidance, and support for getting the proper regulatory certifications so you can sell your products in your desired geographic location as fast as possible. We define a regulatory pathway that suits your business and deliver cost-effective strategies for your specific products.
Year Of Experience
10+
Our Vision
To become a multinational consultancy firm from India, helping clients from India and around the world simplify their journey through ever-evolving regulatory landscapes. We aim to shape the future of healthcare access through strategic insight, collaborative partnerships, and an unwavering focus on global standards.
Our Mission
To empower medical device manufacturers, healthcare innovators, and life science companies to bring their products to global markets with the right regulatory certificates. By delivering expert guidance and end-to-end support throughout the complex process of medical certification, we ensure that safe, effective, and innovative medical technologies reach the patients.
Our Value
We are quick learners and constantly adapt to new regulatory rules and developments in the medical industry around the world. With years of experience, our multidisciplinary team brings broad visualisation to every project by understanding the technical requirements and the strategic impact of regulatory decisions and offering a well-rounded approach that combines engineering, clinical, and regulatory expertise. We are committed to adhering to global compliance standards and ethical practices.
Number speaks everything
Our numbers tell a story of growth, trust, and proven success. Every result reflects our expertise, commitment, and measurable impact.
2k+
Complete Project
20+
Countries Served
950+
Clients Served
250+
service offerings
Why Choose Medreg
Expert consultants, thorough regulatory insight, and a seamless path to compliance, that’s our promise for your medical devices.
Focused on Your Goals
Your challenges guide our approach. By actively listening, we design focused strategies that deliver measurable, result-driven outcomes.
Simplifying Complexity
We decode Complex regulatory requirements and define a clear, actionable pathway, to ensure your projects move forward efficiently and compliantly.
Comprehensive Understanding
We dive deep into your requirements, identifying all critical factors to ensure our solutions address every aspect of your regulatory needs.
Documentation You Can Trust
As experts, we provide clear, accurate, and accessible documentation, keeping you informed at every stage of your project.
Certification Success, Without the Stress
Compliance Made Simple–Start with a Free Consultation
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