It is the responsibility and authority of the Quality Control Department to accept or deny all parts, drug product containers, seals, in-process materials, packaging content, labeling and drug products; We will check the production records to ensure no errors have occurred or that they have been thoroughly reviewed if errors have occurred. The quality control department shall be responsible for approving or rejecting drug products manufactured, processed, packed, or held under contract by another company.
The quality control department shall have at its disposal adequate laboratory facilities for testing and approving (or refusing) components, drug product containers, closures, packaging materials, in-process materials, and drug products. It is the duty of the quality control department to accept or reject all procedures or requirements affecting the identity, strength, consistency, and purity of the drug product. Such prescribed protocols shall be implemented in written form, according to the duties and procedures specific to the quality assurance department.If you wish to learn more about this, visit Quality Control the Label
Every person working in the quality control department shall have, or some combination thereof, education , training and experience to allow that person to perform the assigned functions. The training shall be in the specific operations performed by the employee and in the current good manufacturing practice. Training in current good manufacturing practice shall be continuously and with sufficient frequency conducted by qualified individuals to ensure that all employees remain familiar with the CGMP requirements that apply to them. There shall be an sufficient number of trained staff in the quality assurance department to conduct and supervise all operations.