Licensing & Registration

Medical Device Manufacturing Facility layout Planning & Facility Setup Service We at Veteran Provide Facility Designing Services for Medical Devices Manufacturer Complying with National & International Standards of: Medical Devices Manufacturing (Sterile & Non-Sterile) Cleanrooms HVAC Systems Water Systems Compressed Air Systems Lab Equipment/ Instruments

Indian and European Authorized Representative for Medical Devices Manufacturer The EAR is a person/company that is appointed by the Indian Manufacturer who wants to CE Mark /Register/Sale their Medical Device in European Economic Region. Indian Manufacturers of Medical Devices who want Approval for Distribution of their Medical Device in Europe must appoint an European Authorized […]

Import & Export Licenses for Medical Devices and Drugs We have Experienced and Enthusiastic Professionals that help your Organization to get registered your Facility and Devices as per various Country Regulations in Shortest Possible Time and Cost-effective Way. Sugam Portal Registration Our Team of Experienced Professionals will be Happy to Serve you for Sugam Registration […]

Online CDSCO Manufacturing and Import Licence & Certificate through Sugam Portal Our Veteran Professionals are familiar with all aspects of Medical Device Regulatory Compliance in India. Our services include Obtaining Various Licenses and Certifications for Medical Devices- Grant of Mfg. Lic in Form MD-5 : License to Manufacture for Sale or for Distribution of Class […]

Import Licence for Pharmaceuticals & Cosmetics Manufacturing Licences for Pharmaceuticals and Cosmetics in form 25 , 28 & 32 Whole Sale Lic for Drugs Uploading of Pharmaceuticals Formulation on Sugam Portal Device Master File Preparation, Plant Master File Preparation, Technical Construction File and Design Dossier Preparation New Drugs Approval Clinical Trial Registration of Drugs in […]

We have Experienced and Enthusiastic Professionals that help Your Organization to prepare the following Documents Customized with your Organizational Processes in Respect to Indian Drug and Cosmetic Act’s Schedule-M, Medical Device Rule 2017,European MDD/93/42/EEC Amended by MDD/2007/42/EEC, EuMDR 2017-745, IVD EuMDR 2017-746, MDASP, US FDA Quality System Regulations. We at Veteran provide you Technical Document […]

Export Registration and Approval We have Experienced and Enthusiastic Professionals that help your Organization to get registered your Facility and Devices as per various Country Regulations in Shortest Possible Time and Cost-effective Way. African Countries Ghana, Nigeria, Benin, Burkina Faso, Central African Republic, Congo, Egypt, Ethiopia, Gabon, Liberia, Malawi, Morocco, Rwanda, Sierra Leone, Sudan, Tanzania, […]

ISI Registration ISI Marking for Medical Devices, Medical Equipments and all article under compulsory & Voluntary certification (Medical Beds, OT Light, OT Table, Incubators, ICU Equipments , Surgical Dressing, Surgical Bandage etc.)

GeM (Government E-Marketplace) & NSIC Registration Company Registration Profile page completion Vendor Assessment Brand Approval Catalogue Approval (Product uploading)

USFDA 510k Submission & Device Listing FDA Establishment Registration FDA Device Listing for Class I (510(k) Exempt Devices) FDA 510(k) Approval CFG USFDA