RegCheck™ Benefits

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

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