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VOL P. 65M O ND A Y, J U L Y 6, 2 0 2 0THE LEGAL INTELLIGENCE 13PUBLIC NOTICES Brian Harris215.557.2496ESTATE NOTICESNOTICE TO COUNSEL Your attention is directed to Section 3162 of the Probate, Estates

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What is m o nd a?

M O NDA is a regulatory document that pertains to the approval and commercialization of new drugs and biological products in various jurisdictions.

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Any entity or individual seeking to obtain approval for a new drug or biological product must file an M O NDA with the relevant regulatory authority.

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Filling out an M O NDA involves providing detailed information about the drug, including its composition, preclinical and clinical study results, manufacturing processes, and proposed labeling.

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The purpose of an M O NDA is to ensure the safety, efficacy, and quality of new drugs or biological products before they can be marketed to the public.

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An M O NDA must report information such as drug formulation, clinical trial data, safety and efficacy results, manufacturing details, and proposed marketing information.