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Navigating Chemistry, Manufacturing, and Controls Through the Drug Development Process

Register for this On-demand Training Course which will demonstrate CMC sections of regulatory submissions, the FDA inspection process, and how to avoid or minimize 483s (noncompliance) using real-life scenarios.


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  • Priya  Jambhekar

    Priya Jambhekar

    • President
    • PBS Regulatory Consulting Group Inc., United States

    Priya Jambhekar has over twenty years of experience in the areas of product development, product safety, quality assurance, quality compliance, Clinical operations, supply chain management and US and international regulatory affairs in handling new and me too products globally. She has extensive experience in establishing regulatory strategy for Chemistry, Manufacturing Controls, Clinical and Nonclinical development for first in the class products and operational excellence for optimal success during all aspects of pre- and post- approval phases of new drugs, devices, and biologics development and marketing of products. Priya is also certified by RAPS and NJ Pharmaceutical Quality Control and Assurance Society

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