1.7 - Self Inspection via Internal Audits material storage or drug products shall not

or drug products shall not be reactive

Quantitative test methods must be validated by determining in assays the sensitivity

Laboratory records shall include complete data derived from all tests necessary to assure compliance with established specifications and standards

Sufficient space should be given to avoid mix-ups and cross-contamination

or any contact surface

1.7 - Self Inspection via Internal Audits material storage or drug products shall notSelf inspections should be conducted in order to monitor the implementation and compliance with Good Manufacturing Practice principles. and to propose necessary corrective measures, at intervals following a pre arranged programme in order to verify their conformity with the principles of Quality Assurance