As the last step in the process of building a production plant, and once all of its facilities and production and installed machinery are finished, you need a full program of commissioning and validation of all components in order to ensure that all processes, equipment and facilities operate according to the specifications.
The entire process should be properly documented according to international standards in order to facilitate the approval processes of local and / or international pharmaceutical authorities.
Reception and commissioning of all facilities and equipment
Validation Master Plan (VMP)
Validation IQ / OQ / PQ
Management of Technical Documentation
Approval of pharmaceutical, local authorities, EU GMP/ FDA
We have been able to build a client base for ourselves across the country with the help of our quality range of air equipment.
Our professionals are employed only after we test them on the basis of their domain expertise, skills and industrial experience.