Internal regulatory strategy meeting to outline

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Reference no: EM132307880

Your company is acquiring a new product (you can pick any hypothetical product). The previous developer did not seek any expedited review or meet with FDA or users. The Phase 2 study had promising results. You have been asked to speed its approval by any means. You plan to hold an internal regulatory strategy meeting to outline your approach including how your product meets the FDA criteria for the action you are requesting. You are to submit your proposed regulatory strategy in writing. Write a Internal Regulatory Strategy Meeting request to discuss speeding FDA approval of newly acquired drug.

Reference no: EM132307880

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