Medical Device Consultant in India
One of the leading Regulatory Compliance Consultants providing services to get Licence to Manufacture, Import, Test, and Wholesale Medical Devices & Pharmaceuticals, ISO & CE Certification, US FDA Registration & 510K Submission, UDI Labelling, and EUDAMED Registration.
MedDev Experts is a Regulatory Consulting Organization that provides regulatory advisory & guidance to various manufacturers, exporters, and importers in the Medical Device & Pharmaceutical industry. We provide service to implement Quality Management Systems, Licensing, Regulatory Approvals, and Certifications within budget and timeline. We provide a complete solution to our customers who are looking to set up a world-class manufacturing unit. We have a team of experts whose knowledge & experience helps them handle clients both small & large.
Find Peace of Mind with MedDev Experts
Your Trusted Regulatory Partner
We provide complete guidance to get your Drug, Cosmetics, Manufacturing & Loan Licence, Food Manufacturing Licence (FSSAI), AYUSH Licence, Drug Wholesale & Retail Licence. We support to get your new drug approval along with all certificates.
Our highly experienced and passionate team supports getting your Licence for Class A & B and Class C & D Medical Devices to Manufacture, Import, Test, Wholesale, & Clinical Trial within the shortest possible time at a reasonable price.
We provide support to get you Establishment Registration, Product Listing & Certification, NDC Labeler Code, User Fee (GDUFA), Registration of Medical Device Facility, Listing of Medical Devices, Annual Registration Renewal, and 510K Submission.
We provide guidance to get certify your quality management system. We assist your organization to comply with the standards to get the certification of ISO 13485, ICMED 13485, ISO 9001, ISO 22000, SA 8000, and ISO 14001.