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Manufacturer of Food, Drug, and Medical device requires US FDA registration for their facilities. US FDA Registration is only needed if you are planning to market your products in the USA.

The FDA regulates many products that are intended for human consumption, including food and medical devices. In addition to registering your product with them, you will also need to comply with all other applicable laws and regulations.

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  • Home
  • About
  • Services
    • Management System Certification
      • ISO 9001:2015
      • ISO 14001:2015
      • ISO 45001:2018
      • ISO 27001:2018
      • ISO 20000:2018
      • ISO 28000:2022
      • ISO 13485:2016
      • ISO 22000:2018
      • ISO 50001:2018
      • ISO 31000:2018
      • IATF 16949:2016
      • HACCP
    • Product Certification
      • CE Marking
      • PED Certification
      • HALAL Certification
      • KOSHER Certification
      • RoHS Certification
      • FCC Certification
      • Ingress Protection (IP) Marking
    • Compliance Auditing
      • GMP Certification
      • C-TPAT Certification
      • GDP Certification
      • Fire Safety Audit
      • Factory Compliance Audit
      • SEDEX
      • SA 800
    • Trainings
      • Lead Auditor Training
      • Internal Auditor Training
      • Awareness Training
    • Registration
      • US-FDA Registartion
      • FSSAI Registartion
      • COMPANY Registartion
      • NSIC Registartion
      • TRADEMARK Registartion
      • TRADE Licence
      • ISI Mark
      • BIS Registartion
      • FACTORY Licence
      • MPCB Registartion
    • Corporate Legal services
      • Business Establishment
      • Corporate Finance
      • Labour Law
  • Contact Us