+61 3 8678 1702 info@qiksolve.com

ISO 9001 Quality Management System Consulting

ISO 9001 quality management consultants

QikSolve is a small team of Quality Management System (QMS) experts with proven industry experience. We are passionate about providing efficient and streamlined document control systems for your organisation.

We believe that a thorough grasp of your business, your challenges and your opportunities are crucial in delivering a QMS that is best suited to your business needs and we will work closely with you to to determine your routine process flows and critical process requirements in order to achieve this.

Contact us for more information

What do we offer?

Extensive industry experience

Our team has a broad range of experience with setting up and running QMS from a variety of industries including medical devices, healthcare, logistics, food and pharmaceutical manufacturing. Because of this, we can offer demonstrated, best-practice solutions to your organisation.

Consulting services for the new ISO 9001:2015

If your organisation is currently certified to ISO 9001:2008, you will need to update this to the 2015 version before September 2018. We can assist you with this process, as well as helping you to understand how the changes may impact your organisation. We are also able to offer consulting services for other standards including ISO 14001, OHSAS 18001 and AS/NZS4801.

Assistance with QMS certification

We can assist you with the certification process by providing expertise on the relevant regulatory guidelines as well as helping you to understand the certification process and timelines. We can also make contact with certification bodies on your behalf and provide ongoing support as required.

Electronic document management system

SharePoint has long has been used as an out-of-the-box document management system. We have taken this, and developed a cost-effective electronic document management system called Ibiqs which includes automated change request, review and approval workflows that aligns with ISO and GMP compliance requirements.

Technical writing

We have experienced technical writers on hand who can help you develop your QMS documentation, or update your existing documentation. We can also provide assistance with process mapping to identify non-value adding activities to ensure that your management system is lean.

Gap assessments

If you have an upcoming surveillance or re-certification audit, are looking to certify your QMS formally or need assistance to identify non-value adding processes in your QMS, we can assist you with all of these needs and more. Our quality system consultants can conduct Gap assessments and give you advice on how you can address the missing links.