Zuellig Pharma Quality Roadmap
Our quality roadmap, focused on People, Process, and Technology, ensures we meet our quality objectives. It's regularly updated to keep up with compliance requirements and changing business landscape.
Forward-Thinking Industry Quality Leadership
We build strong quality culture in the pharmaceutical industry through agile people development, while supporting organisation Quality Assurance needs to meet strategic business goals and driving digital enablement.
Quality Leadership Gives Clear Competitive Advantage
We offer transparent career pathways to make Quality Assurance a vocational choice among employees, as we attract talents who can effectively deal with the escalating complexity of compliance in the pharmaceutical industry.
Value Creation through Quality Leadership
We model Quality Assurance competency as an integral part of our human capital development and establish ourselves as recognised thought leaders in the quality process, both internally and externally.
Digitally-Enabled Quality Risk Management
We develop quality risk management teams who are natural digital natives with Zuellig Pharma Quality 4.0 being fully integrated in the company’s technology landscape.
Quality Expertise Leveraged Across Clients, Governments, Regulators, Educators
We are recognised as Quality experts in the industry across the region and our Quality Management System is viewed as the pharmaceutical industry gold standard.
We adhere to the highest ethical standards across our network to ensure patient safety, data privacy, and an uncompromised supply chain for your products. The safety and reliability of our services ensure that the drugs that are administered to patients have been handled with the highest levels of care.
Our Quality Management System is designed around the requirements of key regulatory bodies, such as the MHRA and EMA from Europe, US FDA, the WHO, PIC/s and ICH.
- GMP Certification
- GDP Certification
- GDPMD Certification
- ISO 9001
- ISO 13485
- ISO 14001
- ISO 45001
- ISO 27001
- TAPA FSR - 2017 Level A
Importer/ Distributor/ Wholesaler Controlled Drugs
- Importer/ Distributor/ Wholesaler Medicinal Products
- Importer/ Distributor/ Wholesaler Cytotoxic Products
- Importer/ Distributor/ Wholesaler Medical Devices
- Manufacturing license (Secondary Repackaging)