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Your Guiding Hand for Regulatory Affairs Processes, Every Step of the Way

Our leading consultants in biotech and pharma can save you time and help secure regulatory approval for your product in the US, Europe, Israel and across the globe.

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International Biotech Consultation and Execution Strategy, Submission & Approval and everything in between

    Regulatory AffairsEarly StagePre-clinicalClinicalRegistrationMarket
    Regulatory Strategy Develop a regulatory strategy for drug development and approval in European, US, Israel and Rest of the World (ROW)
    Manage interactions with regulatory authorities, balancing client’s strategy and regulatory authorities’ expectations
    Initiate and perform consultation meetings with regulatory authorities and Notified Bodies, (e.g. scientific advice meetings, pre-IND, EOP2, etc.) throughout the product development lifecycle
    Prepare and submit regulatory documents, (e.g., IND, IMPD, BLA, MAA, RFD, Technical File, Orphan Designation, Pediatric Plan, expedite programs designations as PRIME and Breakthrough and more)
    Consult on clinical trial design and interpretation.
    Writing and Compilation of clinical study documentation (e.g., IB, clinical protocol CSR, etc.)
    Regulatory, CMC, Pre-clinical and Clinical Gap assessment
    Indication assessment for the potential drug in development from a scientific and regulatory perspective
    Planning Non-clinical program including study design and interpretation
    Product classification according to regulations and classification submissions
    Provide regulatory input to manufacturing and control processes requirements
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