Intro

RegCheck™ Benefits

First column


Provides a standardized, proven method for a user to objectively evaluate drug documentation and identify deficiencies


Helps to avoid costly late-stage rework and potential delays prior to regulatory approval


Provides easy reference for users by annotation to applicable 21 CFR and guidance documents

Second column


Detects potential issues that could prolong or derail health authorities’ review and approval


Identifies deficiencies that can then be compiled and prioritized for timely action


Pairs all identified deficiencies with required or suggested corrective actions that reflect current guidelines and regulations

 

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