Quality control first

Our Quality Control Laboratories identify and analyze each batch of material received from our suppliers according to the specifications and analysis methods defined in our Drug Master Files (DMF). After the fulfillment of all analytical needs, the material are released to be used in production processes.

In the same way, each individual batch of active pharmaceutical ingredients manufactured by MOEHS
it is analyzed according to pharmacopoeial procedures or, failing that, with developed and validated methods.

The Quality Control laboratory applies the analysis methods and contrasts the specifications
of the product with the documentation issued and approved by the Quality department. We keep
analysis files for 11 years and sample preservation for 6.

After releasing the batches by the Quality department, Quality Control issues the Certificate of Analysis and the labels that will identify the product drums.

The Quality Control laboratory is equipped with the most modern analysis equipment and qualified analysts for the development of analytical tasks.