Recertification of our ISO 13485 standard
We’re pleased to share that we have re-certified our ISO 13485 accreditation, which relates to medical devices. This accreditation enables us to handle medical devices safely within our warehouse.
What is the ISO 13485 standard?
The ISO 13485 accreditation enables us to meet safety and quality standards for all medical devices. In this industry, it is vital that safety precautions are taken to ensure that devices remain clean and in good working order.
This standard helps to ensure that all medical device products retain their quality throughout their lifecycle.
How we re-certified the standard
Our dedicated Compliance Manager, Marc, has organised the recertification of our ISO13485 standard. Here’s what he has to say about it.
The ISO 13485 Medical Devices re-certification audit was a comprehensive review of the procedures, policies, training, awareness, and governance of all the component parts of the system we have created to align ourselves with the ISO 13485 standard.
The ISO certificates work on a three-year schedule, with regular auditing taking place between each certification period.
LRQA spent four days on site carrying out interviews, looking at documents, procedures, systems and verifying that everything we do and say we do is compliant with the international standard.
After four days of scrutiny, I’m very pleased to say that the outcome was positive. Following further verification, we will be awarded a new ISO 13485 certificate and a new three-year schedule of audits for our calendars.
This is a brilliant and difficult-to-overstate result. Thank you to everyone who took part and engaged so professionally and confidently in explaining their roles within the system.”
Why do we need to meet safety standards?
As your dedicated brand fulfilment partner, it’s crucial that we take steps to ensure safety standards are met and quality is maintained in all of your products. Having this safety standard in place allows us to offer a trusted and professional service to you.
Maintaining international standards
The ISO 13485 certification is recognised on a global scale. This provides our clients with confidence regardless of where their business operates from. It means that all companies should be following the same standards and taking the same steps to ensure safety and best practices when it comes to medical devices.
Reduced recalls
If a product does not meet safety standards, it is likely to be recalled. In the medical industry, it is vital that products are safe for use to ensure patient safety. Increased product recalls not only increase costs and cause reputational damage, but they can also cause issues with your supply chain.
We provide high-quality supply chain management services, ensuring that your products are stored, packed and distributed safely and efficiently. We can also provide support for reverse logistics should you require it.
Increase productivity
Having a quality management system such as this one in place ensures that everyone involved is working to a standard and taking the correct steps. Streamlining processes is more cost-effective and saves time. Our warehousing and distribution team ensure that all safety precautions are taken care of.
How can we help your business
Granby is your dedicated, brand fulfilment partner. We provide a wide range of third-party logistics services, including handling and fulfilment, warehousing and distribution, contract packing and eCommerce solutions.
We have supported many global brands with our brand fulfilment services. Contact us to see how we can support your business.