What's New Notice regarding Guidance for approval Covid-19 vaccine in India for restricted use in emergency situation which are already approved for restricted use by US FDA EMA, UK MHRA, PMDA Japan or which are listed in WHO Emergency use listing 15th April,2021 DCGI Message 202101 Jan 2021 For Medical devices which are under voluntary registrations, the file number generated is the ...

List of Documents Required for Grant of Registration Certificate for import of Cosmetics into India (For Details please refer Guidance Document) Covering Letter mentioning the purpose of application

5. Application in Form-44 duly filled and signed by the competent authority 6. Treasury Challan of INR 50 ,0 0 0 /- upto 1 year from initial approval and INR 15,0 00 /- for other drugs upto 4 years 7 a. For manufacturing:- Copy of manufacturing license in Form-25/ Form-26 for any bulk drug to manufacturer and Form-29 7b. For import:-

Sugam builds a comprehensive database of the various permissions and licenses issued by State FDAs. This includes details of manufacturers, manufacturing site and drug formulations. Manufacturer can view their consolidated data about permissions issued to them from State FDA. Go through the documents to get your Answers !!!

S.No Name File; 1. Online Payment User Manual: Online Payment User Manual v1.0.pdf: 2. How to Import Non- Registered Drugs for Personal use in India (Form 12A)

User must upload necessary documents like ID Proof Details, Power Of Attorney, Corporate Address Proof and Manufacturing License or Wholesale Licenses (Form 20B & Form 21B) Details and user should keep these documents ready in PDF format before sign up process.

from CDSCO officials and track their application status. It will also enable CDSCO officials to process the applications, generate note sheet, and raise queries and issue approvals / permissions online. The purpose of the document is to specify in detail the Processing of applications of medical devices by the regulatory authority (CDSCO and SFDA).

Sep 22, 2024 · Filling of Application Form: The primary document for cosmetic registration is the application form. The form is filled out carefully and all the details about the product and manufacturer should be mentioned in detail to avoid any …

Welcome to our comprehensive guide on what are Form MD-26 and MD-27 as per CDSCO, the importance of these forms, and how they streamline the process of importing medical devices in India, ensuring your medical device meets regulatory standards.

Central Drugs Standard Control Organization Directorate General of Health Services Ministry of Health & Family Welfare Government of India. Home. About Us ... (RC form 41) Biologicals: 2016-Jan-11: 64kb: 25: Pre-screening Checklist for Medical Device(Registration Certificate) Medical Devices: 2016-Jan-11: