Professional Know-How You Can Trust

A successful business operating in the highly regulated therapeutic goods and health sciences sector requires a clear understanding that compliance must be maintained without compromising quality, safety and efficacy. Misunderstood requirements and sub-standard systems, processes, facilities, record-keeping and personnel training can result in negative impacts and avoidable costs.

Choosing the Benchmark Quality Systems team of professionals for your project means that you can rely on years of hands-on industry experience gained in world-class pharmaceutical facilities operating under the code of Good Manufacturing Practice (GMP) and the requirements of major government regulatory agencies (TGA, FDA, EU). Our team of specialists can provide you with subject matter expert advice and support in multiple areas:

• Regulatory Affairs

• Quality Systems Development and Implementation

• Engineering, Project Management, Process Design and Facility Design/Construction

• Validation and Verification of Systems, Processes and Equipment

Developing and maintaining a fully supportive client-partner relationship is the cornerstone of our philosophy. Whether start-up or established, the Benchmark Quality Systems approach will ensure that your project scope, timelines and outcomes are clearly defined and understood. From commencement until completion and handover, transparent communication is assured, as is the availability of Benchmark Quality Systems team members for progress updates and consultation.

Without obligation and with full confidentiality, we invite you to discuss how our expertise can support the delivery of your project.