Dr. Pharm's production system has passed ISO 9001 quality management system certification and is deeply integrated into the essence of Good Manufacturing Practice (GMP) for pharmaceutical production. We consider safety and compliance as an uncompromising lifeline:
Environment controllable: Key assembly areas meet clean room standards and control particles and microorganisms.
Process controlled: Implement three-level quality control including first article inspection, process inspection, and final inspection to ensure manufacturing consistency.
Record keeping: Establish complete material batch numbers, production batches, inspection records, and equipment calibration files to achieve full process traceability.
Verification support: Provide detailed DQ/IQ/OQ/PQ (design/installation/operation/performance confirmation) document templates and support services to accelerate the customer equipment verification process.
We not only deliver equipment, but also production guarantees that comply with regulatory requirements, have controllable risks, and can withstand audit tests, allowing customers to focus on drug research and development and production without any worries.