It is important to note that pharmaceutical laboratories are currently operating under non-GLP/GMP conditions, particularly for assessing solid oral dosage forms such as tablet and capsule products. This is surprising that such negligence has been going on unchecked. This deficiency needs to be corrected so that facilities can be considered QC/QA laboratories to provide the products’ relevant and accurate quality characteristics. For further details, please follow the links (1, 2, 3).