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CALL FOR ABSTRACTS Due by Friday, November 1 Regulatory Information Management 2014 February 2526, 2014 CALL FOR PRESENTATION ABSTRACTS ABSTRACT SUBMISSION DETAILS and GUIDELINES SUBMISSION DEADLINE:
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Regulatory Information Management refers to the processes and systems used to manage regulatory content, submissions, and compliance requirements.
Companies in regulated industries such as pharmaceuticals, biotechnology, medical devices, and food and beverage are required to file regulatory information management.
Regulatory information management forms can be filled out electronically or in paper form, following the instructions provided by the regulatory agency.
The purpose of regulatory information management is to ensure compliance with regulations, maintain product safety, and facilitate communication with regulatory agencies.
Information such as product details, manufacturing processes, safety data, and compliance records must be reported on regulatory information management forms.
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