CDSCO Registration FAQs
Who can register for CDSCO online portal?
Corporate, Indian Agent, Importer, Foreign Enterprise holding Indian Subsidiary, Cosmetics, Ethics Committee, Formulation R&D Organization, BA/BE Approved Sites, Sponsors(BA/BE & CT)
How will I login to CDSCO online portal ?
Frist go to homepage and check on ‘sign in’ under with you will get a link named ‘Sign up Here’ then fill the details and upload the document required with a proper official email id on with all the correspondence activity’s would be done. After your email id gets verified then check further action on register email id. Where you are been required to send the hard copy of document submitted. After which you will get your login credentials on register email id.
- Operon Strategist is Medical Device Consulting. we can assist the manufacturer in the process of cdsco registration.
I am not able to receive Email or SMS service from CDSCO Portal?
Check your Junk/Spam folder, so if you receive mail in junk/spam folder then save “ cdscoonline-noida@cdac.in” in your contacts and if not, then please contact to Administrator by “Report a problem” section on home page of CDSCO Portal.
If you have selected the option to receive SMS at the time of registration then only you will receive SMS alerts. If done check DND (Do not disturb) settings in your phone. If not, then please contact to Administrator by “Report a problem” section on home page of CDSCO Portal.
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Contact details –
Phone no - 93702 83428
Mail id – enquiry@operonstrategist.com
Phone no - 93702 83428
Mail id – enquiry@operonstrategist.com
- Medical Device Consulting
- cdsco registration
- FDA 510k Clearance
- ce mark medical device
- CDSCO Manufacturing License
- CDSCO import license
- TURNKEY PROJECT CONSULTANT
- medical device manufacturing
- iso 15378 certification
- 21 cfr part 210 and 211
- ISO 13485 Medical Device Consultant
- Primary Packaging Turnkey Project Consultant
- Clean Room Design Consultant
- manufacturing site conceptualization
- Market Analysis and feasibility for Medical Devices
- manufacturing plant layout design
- medical device design and development
- DMF file submission guideline
- 21 cfr part 820
- qms certification services
- capa management
- design control requirements
- medical device process validation
- combination product
- continuous improvement program
- Medical Device Compliance & Regulatory Services
- Cdsco India authorized agent for medical device
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