8.1 - Laboratory Overview Sub-Part P or other investigations prove the

or other investigations prove the drug product meets appropriate standards of safety

Labeling materials issued for a batch shall be carefully examined for identity and conformity to the labeling specified in the master or batch production records

or contact surfaces from becoming contaminated

You must use adequate laboratory facilities to perform whatever testing and examinations are necessary to determine that specifications are met

8.1 - Laboratory Overview Sub-Part P or other investigations prove theThere must be at least one laboratory, independent from Production to permit the satisfactory operation of Quality Control. Laboratory operations must be under the authority of a person with appropriate qualifications and experience. Adequate resources must be available