Steps to Fill out the Form
Step 1: Fill out the MD-7 form by going to cdscomdonline.gov.in.
Step 2: The next step is to pay the fees.
Candidates may use the government treasury challan to pay their fees under the head of the account.
The costs of the production plant are $50,000, whereas the costs of the goods are each $1,000.
Step 3: the second component of the technical documentation and the required documents for the fourth schedule.
An application letter, cover letter, andcoverllan receipt are all required.
Information about the company's partnership, a property declaration, a list of partners, including their ages, and complete mailing addresses. Documentation demonstrating site ownership and tenant agreements.
Under the declaration of the manufacturing and analysis chemists, the educational institution has included the plant manufacturing data listed in appendix I.
Device master files for every product are in line with appendices II and III of the fourth schedule, along with a performance review report, if applicable.
Test the license copy only when necessary. The creation of the website by the timetable.
Step 4: Post each document on the web page of the ministry of health and family welfare.
Step 5: Analyzing the work that CLA does.It takes about 40 days.
Any discrepancy is recognized, and a query is presented.
The next action is taken after receiving the applicant's response.
Step 6: Officers and medical device specialists conduct audits in manufacturing facilities.
It will take around 60 days to finish.
The applicant may make any necessary corrections if there are any errors.
If it is deemed acceptable, the audit report will be sent for more action.
Step 7: CLA renders a judgment.
If CLA is satisfied with the report, Form MD-9 is used to grant a manufacturing license.
Within 45 days, if CLA is unsatisfied with the report, it will reject the application and justify it. it
Version 1.2 of the license Five years is the validity period for the MD-9 form.
The applicant has 45 days from the auction date to reapply if the license is ever suspended or revoked.
Zones and the CDSCO headquarters process for applying for a manufacturing license Type MD-7.
A nodal officer can view the new application under the "new application" tab.
The reviewing officer is assigned to the application by the nodal officer who files the inspection report.
If the first reviewing officer is not available, the Nodal officer may forward the application to another review officer.
Under the new program, a file reviewing officer has access to the file.
The review officer creates the note sheet after examining or modifying the checklist.
The application is given to the zonal DDA.
Zonal DDA prepares the note sheet after once again analyzing the information.
The application is forwarded if the nodal officer of their related zone uploads the inspection report.
The file is once again assessed at the DA of HQ. A memo is written and sent to the NO/DDA of the Zone or the LA/RO/SRO of the HQ.
LA reviews the text again, makes a note sheet, and then gives it the go-ahead.
If the application is incomplete, LA rejects it and opens an investigation.
The final reviewing officer receives the application, creates the authorization, signs it digitally, uploads it, and updates the status to "authorized."
Loan Licenses for Class C and D Medical Devices: Forms MD-7 and MD-9 Application Procedures
