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A modern GMP-compliant veterinary pharmaceutical facility combining advanced production technology with rigorous quality systems.
Our production facility is designed and operated in accordance with Good Manufacturing Practice requirements applicable to veterinary pharmaceutical products. The facility supports dosage form manufacturing lines with dedicated production areas, quality control laboratories, and temperature-controlled warehousing.
The published poultry product range currently includes the following dosage forms.
Oral solutions and concentrates for administration via drinking water, as listed in the Divine Pharmaceuticals poultry catalogue.
Water soluble powder formulations for precise dosing through drinking water systems.
All incoming raw materials are received, tagged, and quarantined pending quality release.
Identity, purity, and specification testing is conducted by our QC laboratory before approval.
Approved materials are accurately weighed and dispensed in controlled environments by trained staff.
Production proceeds using validated batch manufacturing records and qualified equipment.
Critical quality parameters are monitored at defined intervals during production.
Bulk product is sampled and tested against specification before proceeding to packaging.
Primary and secondary packaging is applied under controlled conditions with label verification.
Qualified person signs off on the complete batch record before product is released.
Explore the controlled workflows used across materials handling, production, quality testing, microbiology and finished-goods release at Divine Pharmaceuticals.
Each process is structured around defined QA/QC checkpoints, approval stages and controlled movement through manufacturing.
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Raw material enters the controlled RMS & PMS material-handling workflow.
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Raw material enters the controlled RMS & PMS material-handling workflow.
Rejected
Approved
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Raw material enters the controlled RMS & PMS material-handling workflow.
Our R&D team works on formulation development, product improvement, and stability testing to continuously advance our veterinary product range. New formulation work is conducted in adherence with applicable regulatory guidelines.
Our manufacturing facility is structured to support export market requirements. We can provide the documentation, labelling adaptation, and batch certification required for international registration and distribution.
Submit Export Inquiry