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    Building Blocks

    Regulatory Affairs Services

    We have a dedicated regulatory affairs team to ensure the regulatory compliance of your projects. Team members are trained in areas of R&D, GMP compliance, and registration, with 50+ DMF, ANDA, IND and NDA submission and approval experiences, covering 10+ markets including China, US, EU, Japan, etc.


    ?  Original submission: preparation and submission of registration dossiers and related documents for API intermediate, API and drug products

    ?  Reply to the deficiency letter: preparation and submission of response to the deficiency letter from agencies

    ?  E-CTD formats and submission, if required

    ?  Post registration dossiers maintenance: amendment and annual report submission, and any other communication needed during a product life-cycle

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