We have over 35 years in Medical Device Product Registrations,Quality Management and Process development in the Healthcare Industry.
Our forte is our continual training on updated regulatory requirements, our deliberations in various committees in association with our collaborating partners for a globalised and harmonized registration framework and the implementation of best practice excellence in Quality System maintenance.
We are well known at both a local and global level with involvements with a number of companies ranging from the start up company to multinational manufacturing facilities in Europe, US and the Asia Pacific region.
Our unique core value proposition is endowed in our belief that your continual needs must be exceeded beyond your expectations and we will deliver to your requirements within your agreeable timeline and budget.
We take humble pride in working with our new and long term clients using a very unique and differentiated relationship approach.
Our capabilities include the most up to date and live state of the art Regulatory Intelligence System with accessibility on who’s who in Medical Devices, Complimentary Medicines, In Vitro Diagnostics, OTC and Prescription Medicines.
Our Intelligence includes background information on more than 85,000 product approvals since the introduction of the current Australian regulations.
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