Small to Medium Sized Enterprizes

Access 7000+ standards and regulations today

 

Small to medium sized enterprises in the Medical Device Sector

With Small and Medium sized enterprizes representing such a large part of medical device manufacturers globally, their existence is vital to patient safety. Increasingly complex compliance requirements for UK, EU and MDSAP jurisdictions can be prohibitive to small to medium sized enterprizes.

Aligning with your requirements, offering a price that works for you.

BSI is committed to supporting this vital portion of the market. We fully understand the difficulty in remaining compliant and placing medical devices on the market. We have helped countless Small to medium sized enterprizes in ensuring they manage their compliance regulatory requirements in a cost effective and efficient way. Our digital workflow tool, Compliance Navigator, is the only platform designed by regulatory experts to help manage your medical device compliance. We offer pricing that works for you, aligning with requirements of smaller organizations, so you can access all the standards you need for your products, plus guidance from BSI experts on updating requirements.

Want to find out more? Simply download our flyer and gain insight into how Compliance Navigator can help you and your team! With over 7000 medical device standards and documents, there’s no better time to try.

Feel like Compliance Navigator is a good fit for you? Request a free trial today by clicking here.

Digital tools that save you time and money

Compliance Navigator holds over 7,000 documents essential for medical device and IVD compliance. With multi-user access, it’s available to your whole team.

Alerts to changing standards

Put your team on the front foot, with alerts for when standards change and advance warnings for upcoming changes to BS standards.

Example alert email

Smart Support and expert commentary

Fast track your understanding of the MDR, IVDR and MDSAP regulations with Smart Support and guidance.

  • You'll also interpret standards correctly with our expert commentaries
Expert commentary

A comprehensive guide MS

You can see the full text of standards, legislation and guidance, so you don’t miss anything important.

  • Access the EU MDR and IVDR as well as MDSAP regulations

A comprehensive guide

Profiles and Templates

You can create regulatory profiles and templates, so you have the information you need in one place, along with links to relevant content outside of Compliance Navigator.

Device-specific profiles

Track changes

You’ll find it easy to see what’s new, with ‘red line’ changes between versions.

Track Changes
Compliance Navigator Strapline