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Quality

Zuellig Pharma SSG Australia meets our client’s clinical trial expectations by combining a high level of commitment to our services, quality, integrity and compliance. We are curious to learn about the challenges you face and eager to collaborate on finding solutions to ensure a successful launch of your clinical product.

  • Strong Compliance with Good Manufacturing Practice (GMP) Standards
  • Installation of Quality Controls in each Process Step
  • Authorised Person Only Premises

Quality Assurance and Control

Operating in a TGA GMP certified facility, our Quality Assurance and Quality Control team place a strong emphasis on compliance and quality. This commitment in addition of strict adherence to international, national and high-quality in-house guidelines, guarantees that your products remain safe.

Furthermore, we are dedicated to understanding your specific needs and challenges so that we can provide tailored solutions to support the successful launch of your clinical products. By collaborating closely, we aim to ensure that every aspect of your trials’ journey meets the highest standard of quality and safety.

Certifications
TGA and GMP Certificates
Auditor Approval
Approved by Multiple Global Sponsors, CROs and Large Clinical Trial Service Providers
Professional Assurance
Pharmacist and Specialized Quality Assurance Staff On-Site
Training
GMP Training Records and Staff Schedules for Each Procedures and Processes
Temperature Control and Cold Chain Management
Temperature Mapped and Validated Facility
Shipping Validation
Validated Containers
Inventory Management and Invoicing System
In-house Management and Invoicing Systems
Quality Management System
Integrated Quality Management System with Zuellig Pharma IT-Plattforms
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