CDSCO Registration FAQs 

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. 

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.   

Read More – CDSCO Registration FAQs

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Contact details –

Phone  no –  93702 83428

Mail id – enquiry@operonstrategist.com

If  You Want Medical Devices Services Consultation For Following.

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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