cGMP Compliance and QA Audits. Upon written request to Oakwood, Edge shall have the right to have representatives visit the Facilities during normal business hours to review Oakwood’s Manufacturing operations and assess its compliance with cGMPs and quality assurance standards and to discuss any related issues with Oakwood’s manufacturing and management personnel.
Appears in 2 contracts
Sources: Master Formulation Development Agreement, Master Formulation Development Agreement (Edge Therapeutics, Inc.)