SUGAM is a single window interface to access online services offered by CDSCO. This portal allows users to update and upload data on their website related to license of drugs & medical device manufacturing facilities in India. SUGAM portal is a single window interface. To apply for any form user, you need to register on the portal first. The comprehensive database of SUGAM portal includes details of manufacturer, manufacturing site etc. The applications which are submitted on SUGAM online portal are approved/rejected by CDSCO. For the registration process applicants need to submit necessary documents on an online portal.
SUGAM online portal allows us to avail ourselves of the following services:
- Online submission
- Review
- Grant of license /permission.
Steps involved in CDSCO SUGAM Registration process:
- Fill in the details given in the registration form and get the login credentials.
- Open the link https://cdscoonline.gov.in/CDSCO/homepage and sign up.
- After signing up provide the purpose of registration
- Upload necessary documents.
- After online registration, applicants need to submit hard copies to CDSCO for the further verification process.
Contact details –
Phone no - 93702 83428
Mail id – enquiry@operonstrategist.com
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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
- 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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