Interpret Saudi FDA regulatory rules, or rule changes, and ensure they are communicated through corporate policies and procedures.
Maintain current knowledge base of existing and emerging regulations, standards or guidance documents.
Review product promotional materials, labeling, batch records, specification sheets, or test methods for compliance with applicable regulations and policies
Determine the types of regulatory submissions or internal documentation that are required in situations such as proposed devices changes.
Compile and maintain regulatory documentation databases or systems.
Coordinate efforts associated with the preparation of regulatory documents or submission to the Saudi FDA.
