Built in Microsoft® Word for easy editing, these templates are the quick and easy way to build a Quality Management System (QMS) compliant with the ISO 13485 standard or QSR 820 regulations.
The templates are used by our consultants in the field and are full of practical guidance and how-to instructions. They are easy to use and will save you weeks, if not months, of time.
Ideal for medical device companies who are preparing to commence manufacture of devices controlled by the FDA, TGA or any other regulatory authority.
Take a preview - here's an extract from the template pack
Template pack is available for immediate download after credit card payment has been approved.
Pack includes quality management system templates for developing Policies, Standard Operating Procedures (SOPs) and Work Instructions for the following areas of your business:
These areas are specified as being essential components of a medical device quality management system by the various regulatory bodies e.g. TGA, FDA.
The ideal resource for a quick and easy do-it-yourself QMS implementation, the template pack includes 35 procedure templates (refer to the list on page 3 of the extract above), 20 form templates and several guidance documents.
Included in the price is two hours of support via telephone or email. Feel confident in the knowledge that if you have questions or get stuck then you can speak to a GMP compliance specialist to set you on the right path.
Our consultants have many years of experience working in the medical device industry. You can benefit from their knowledge of what works and what doesn't when creating and maintaining a quality management system for a medical device manufacturer.
Download a free SOP covering change control for medical device manufacturing. It's included in the template pack but you can download and try it out for free now. Download >>