SMOconnect can provide full regulatory support tailored to your exact requirements. We provide support throughout the product lifecycle, from defining the regulatory strategy, facilitating meetings and discussions with the authorities, to clinical trial approvals, marketing authorization submissions through post-licensing support.

SMOconnect also support the ethics committees for the successful submission and registration at CDSCO. SMOconnect extend close follow up from submission till the registration done in minimum course of period.

Please email your queries to info@smoconnect.com with subject EC registration.