It is the duty and jurisdiction of the quality control department to accept or deny all parts, containers of drug products, seals, in-process materials, packaging materials, labelling and drug products. If you’re looking for more tips, great post to read has it for you. To ensure that no errors have occurred or, if mistakes have occurred, that they have been thoroughly reviewed, they will check production records. It is the duty of the quality control department to accept or deny drug products produced, processed, packaged or kept under contract by another organisation.
The quality control department shall have at its disposal appropriate laboratory facilities for the testing and approval (or rejection) of parts, drug product containers, closures, packaging materials, in-process materials and drug products. It is the duty of the quality control department to accept or deny all procedures or requirements concerning the identity , strength , quality and purity of a drug product. The duties and procedures applicable to the Department of Quality Control shall be followed in writing by these written procedures.
Of person engaged in the Department of Quality Control shall have, or some combination thereof, education , training and experience to allow that person to perform the functions assigned to him or her. Education shall take place in the relevant operations undertaken by the employee and in existing good manufacturing practise. Training in current good manufacturing practises shall be performed on an ongoing basis and with sufficient frequency by trained persons to ensure that all workers remain familiar with the CGMP standards applicable to them. An sufficient number of trained staff shall be given to conduct and supervise all operations in the Department of Quality Control.