8.1 - Laboratory Overview Sub-Part P or break under compression during

or break under compression during storage or transport

cleaning and maintenance

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

8.1 - Laboratory Overview Sub-Part P or break under compression duringThere 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