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Get Online CDSCO Certificate India

CDSCO is a drug regulatory body of India responsible for regulating the import and export of drug products and ensuring that drugs are safe for use. CDSCO Certification is mandatory for all drug importers in India.

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CDSCO certificate is mandatory for all drug importers in India. CDSCO Certification helps exporters, importers, and manufacturers make drug imports & exports between different countries, simplify the procedures involved, and save valuable time and money and the substantial expertise required. We are India’s best CDSCO Certificate Consultants. We have many years of experience in Registration and Certification. Our CDSCO experts will help you solve your problems and take the proper steps to complete the process. CDSCO Certificate Experts will make your CDSCO registration process smooth, transparent, and time-saving. We provide a complete range of services related to the Registration and Import of Drugs into the country. We help you get a Drug registration certificate from the Delhi-based CDSCO organization regarding import permission of drugs, cosmetics, or medicines. We provide the one-stop solution for your business standards to obtain a CDSCO Certificate with all the registration details required. apply for your India Drug Registration today and work on CDSCO registration with our expert consultants. Once you are registered with CDSCO, you will be able to import medicines, cosmetics, and other healthcare products into the country. If, Apply for your India Drug Registration today and work on CDSCO registration with our expert consultants. Once you are registered with CDSCO, you will be able to import medicines, cosmetics, and other healthcare products into the country.

We provide consultation services regarding the Registration, Licensing, Import & Export, and custom clearance procedures under the Drugs & Cosmetics Act 1940.

CDSCO Certificate Rules:

The manufacturer or his authorized agent in India shall inform the licensing authority within 30 days in writing in the event of any change in manufacturing process, or in packaging, or in labelling or  Guidance Document (Import and Registration Division) Document No. IMP/REG/200711   71 | P a g e Central Drugs Standard Control Organization Directorate General of Health Services, Ministry of Health and Family Welfare, Government of India in testing, or in documentation of any of the drug pertaining to this Registration Certificate.

In such cases, where there shall be any major change/modification in manufacturing, or in processing or in testing, or in documentation as the case may be, at the discretion of the licensing authority, the manufacturer or his authorized agent in India shall obtain necessary approval within 30 days by submitting a separate application along with the registration fee, as specified in clause (ii) of sub rule (3) of rule 24-A.

We at CDSCO Certificate are the service providers of CDSCO Certificate, Drug Registration with Import permission for drugs, pharmaceuticals, medical devices & cosmetics through our experts. CDSCO Consultancy Services (CDSCO) provides you with a complete set of services and guidance, including the registration process, essential information, laws and regulations, legalization, processing time, and filing.

A) NOTE: LEGAL UNDERTAKING BY WAY OF AN AFFIDAVIT ON HUNDRED RUPEES NON-JUDICIAL STAMP PAPER

I……………………. S/o…………………………R/o…………………………  aged about………do hereby solemnly affirm and state as under that: – 1. I am working for M/s…………………………in the capacity of…………………and as such fully competent and authorized by the M/s…………………………to swear by way of the present legal undertaking.  2. I legally undertake to state that the product……………………………is manufactured by M/s…………………………… at and the documents enclosed with the application Form-40 are true and correct and nothing contained in it is wrong and false.  3. I legally undertake to state that the Good Manufacturing Practice (GMP) compliance Certificate with respect to the manufacturing site M/s………………………   and   the   product…………………submitted along with the Form-40 has been issued by the Competent Drugs Regulatory Authority of the country of origin that is………………………………

DEPONENT

VERIFICATION

Verified on this day of (Month), (Year) that the contents of my above Legal Undertaking are true and correct and that no part of it is false and nothing material concealed their form.

DEPONENT

The Rules 122A, 122B, 122 DAB, 122DAC, 122 DD and 122E of Drugs & Cosmetics Rules give the information, data required for approval of clinical trial and or to import or manufacture of newly introduced drug for marketing in the country.

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