We follow CGMP and ready for all third party audits
We will provide the documents for CMC (Chemical manufacturing control) section, if required, for submission of DMF.
For all high value, key intermediate supplies, we will conduct the use test in addition to regular analysis to avoid any undesired results in the Pharma stage.
We will provide stability data for all key raw materials of regulatory products for submission of USFDA/ other regulatory authorities.
We shall keep the relevant Impurity samples available to support the customers.