At Paushak, we like to build consistency in our manufacturing process and to have documented quality processes at each stage starting from raw material to customers.

Paushak QA reports to the Alembic group QA head, who is also responsible for our FDA approved formulation and API facilities. Alembic has filed numerous DMF's and ANDAS and hence at Paushak we understand the needs of our customers and GMP requirements for key intermediates. We follow standard operating procedures and have documentation for all critical operations. We follow a documentation control system, CAPA is raised for any deviation and also encourage routine external audits by various agencies.