Your browser is out-of-date!
Update your browser to view this website correctly. Update my browser now
One of the largest manufacturing facility in Northern India.
Strict adherence to GMP & GLP norms without jeopardizing the standards under any circumstances.
Skilled professional at all levels in Q.A, Q.C, Production & Engineering.
Strong focus on new product development.
Strong customer base
Sophisticated labs with all the latest instruments like HPLC, UV Spectrometer, FTIR & many more. Latest Technologies adopted & continual upgradation.
Quality Policy & Quality System Manuals are available which guides the Quality Management System to provide products & services of highest standards with Total Customer Satisfaction. Quality System Manual covers the following areas.
All details regarding QA/QC activities of Plant are included in this document as per requirement of WHO GMP norms. The Quality Manual is Approved by Head-QA and Authorized by Plant Head.
Revision of Quality Manual is done in every two years or whenever required.
Validation Master Plan is available which covers all the aspects of Qualification of facilities, Equipments, Process, Calibration, and Revalidation etc. and documented for future reference.
Revision of Validation Master Plan is done in every two years or whenever required.
All the Documents are Controlled by QA Department with regulated distribution as per the Standard Operating Procedure. Documentation has categorized like, Product / Process Specification, Raw Material Specifications, Packaging Component Specifications, Standard Process Instructions including Packaging, Batch Manufacturing Records and Packaging Records, Analytical Methods, Validation and Qualifications Documents etc. All the documents are stored In-house.