Indian Import License Consultant For Medical Devices
Indian CDSCO Import License - Overview
The Indian Central Drugs Standard Control Organization (CDSCO) Import License is a vital regulatory requirement for importing medical devices into India from other countries. This license ensures that your medical devices meet the necessary quality and safety standards. At Operon Strategist, we specialize in guiding you through the complex process of obtaining the Indian CDSCO Import License, making it easier for you to access the Indian medical device market.
Who Should Apply for Indian CDSCO Import License for Medical Devices?
Applicable when you wish to import medical devices from Saudi Arabia to India. However medical devices need to be classified according to the CDSCO-notified devices list. CDSCO has a complete procedure for granting licenses for medical devices imported into India.
Application Process for Grant of Indian Import License in Saudi Arabia
An authorized agent (who must have a wholesale license for local distribution) having a license to manufacture for sale or distribution or wholesale license for sale or distribution in India under these rules, shall make an application for a grant of import license for medical device to the Central Licensing Authority through an identified online portal of the Ministry of Health and Family Welfare in the Central Government in Form MD-14 for obtaining a license.
Where the Central Licensing Authority, has reason to believe that the quality of the medical device is compromised, and decides to subject to its evaluation, test or evaluation, test or examination, to the testing laboratory as specified by the Central Licensing Authority.
After examining the documents along with the application on the basis of the inspection report, if the inspection done by the Central Licensing Authority can be satisfied, the granted license in Form MD-15 may reject this application for these reasons shall be recorded in writing within the time of nine months from the date of the application.
In the process of rejection, the applicant can make an appeal to the Central Government within the time of forty-five days, and the Government, may after the inquiry in this matter pass an order in relation there within the time of ninety days from the date of appeal.
Medical Device Registration for Import:
Medical Devices entering India must comply with the Indian medical device regulation set forth by the CDSCO Registration. The CDSCO is responsible for approving and regulating New Drugs and Clinical Trials in the Country, laying down the standards for Drugs, controlling the quality of imported drugs, and coordinating the activity of State Drug Control Organizations.
Operon Strategist assists medical device distributors and medical device wholesalers in Saudi Arabia to procure CDSCO import license for medical devices. An Import license is issued for import of medical device from Saudi Arabia to India. Both the foreign company and Indian company jointly needs to submit the documentation for medical device and manufacturing unit.
Looking for Medical Device Regulatory Consultants in Saudi Arabia?
Pre-requisites:
- Generic Name / Brand Name
- Intended Use
- Material of construction
- Mode of application
- Study of device details and Classification of medical devices on the basis of the notified product list of CDSCO
- The class of device helps in determining the application form to be applied and also the application fees.
Indian Import License Application Phases for Saudi Arabia
CDSCO’s import license of medical devices is regulated in India. Any industry or individual with a license (wholesale and manufacturing license issued under the Central Drug Standard Control Organization (CDSCO), Drugs and Cosmetics Act, 1940) can import medical devices into India.
Under the new dispensation, foreign manufacturers have to apply for a CDSCO manufacturing license registration certificate for their manufacturing premises and the individual drugs to be imported. The applications can be made by authorized agents of Saudi Arabian firms in India. The documents required for CDSCO registration certificates have been specified in the amendments. The validity of registration certificates will be 3 years from the date on which these are issued. Contact us for further details
Phases in Indian Import License Registration:
- Phase I – Application Registration
- Phase II – Import License Application
Phase I – Applicant Registration:
In this phase after applying client can have an active account on CDSCO Online System for Medical Devices registration site.
Procedure
First online form has to be filled and all above required documents have to be uploaded. In online form details of manufacturing company like complete corporate address, contact details like email and contact No., fax No., name of authorized person name, ID proof number, Company type (Ltd, Pvt. Ltd etc.), email id for registration, password, alternate email id etc.
Once form submitted, preliminary approval is received from CDSCO and subsequently hard copies submitted will be verified with online submitted information and documents.
Then CDSCO processes the application registration. Based on approval or rejection of application from CDSCO. Mail will be received stating reason for rejection or reapplication and same process have to follow again.
Phase II – Import License Application:
This license is required to have permission to import medical device for commercial purpose.
Procedure
For Application on online portal, form has to be filled with device related information like generic name, brand name, class of device, category of device, packaging configuration, shelf life, sterile / non-sterile, intended use, product description, accessories and model details if any.
After form filling, uploading of all above documents to be done. Then payment as per fee structure of CDSCO has to be done online. Upload payment receipt on online poral then a legal form will be generated based on product information filled and transaction done.
Application submitted will be moved to stage of In-process when review is in-process. Then either application can be approved or if any query raised then that query related revised documents or any justification for that have to be uploaded online against that query. If query compliance is acceptable then approval of test license will be received and email related to same will be send by CDSCO.
Operon Strategist's Expertise
Operon Strategist is the leading medical device regulatory consulting company. We provide regulatory guidance to various manufacturers in the healthcare industry to ensure the strategic development of these manufacturers. We serve our clients by providing turnkey services, system implementation, training, licensing, regulatory approvals, and certifications. Contact us for further details.