The Central Drugs Standard Control Organization (CDSCO) has listed new regulations to obtain clarification on the regulatory status of the Medical Devices. To get this clarification, the importer or manufacturer must submit a no-objection certificate (NOC). The applicant should submit a hard copy of the NOC to the Medical Device division in CDSCO.
Any Importer and local manufacturer can apply for Clarification NOC from CDSCO
The Applicant must follow the following process:
Product details/Description |
Regulatory Certificate from country of origin |
The validity of this is not specified.
To submit a NOC to the Medical Device division in CDSCO, the importer or manufacturer must also submit the following documents:
NOCfrom Central Drugs Standard Control Organisation
Not specified
The importer or manufacturer should ensure that they have listed the exact intended use of the Medical Device as claimed in the instructions for use.
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A clarification NOC is a no-objection certificate issued by the CDSCO, which reflects the regulatory status of the Medical Device in India.
Both importers and manufacturers can apply for clarification NOC