BSI launches new In Vitro Diagnostic (IVD) CE marking service

Press release - Reston, VA. – June 14, 2010

BSI is proud to announce the expansion of its world class Notified Body CE marking services to include the In Vitro Diagnostic (IVD) European Directive 98/79/EC. This new extension establishes BSI as a full-service Notified Body for all European Medical Device Directives, supporting all types of devices including medical, active implantable and now IVDs. BSI has been accredited with a comprehensive scope which includes all In Vitro devices listed in Annex II List A (high risk) and List B (moderate risk) as well as Self Test which are primarily used by lay persons.

IVDs are an essential and fast growing part of healthcare industry. The In Vitro Diagnostics Directive (IVDD) sets the CE marking requirements needed to place IVD medical devices on the European market. IVDs includes devices and accessories used to perform tests on samples, taken away from the body such as blood, urine, tissue, to help detect infection, diagnose a medical condition or prevent disease.

"As technology advances, the divisions between the three Medical Device Directives becomes finer and products may cross over", explains Paul Brooks, Vice President BSI Healthcare. "It is essential that a Notified Body can support clients across all device categories and by extending our scope to include the IVD Directive, BSI will enable customers to work with one organization for all their certification needs."

BSI’s IVD Service is built upon the same successful foundation that has made BSI a leading Notified Body, with a worldwide reputation for delivering services that blends experience with safety, and speed with predictability. "Our new fully resourced in-house team is one of the most experienced within the industry", states Sue Spencer, BSI’s Head of IVD. "Our product experts have an average 17 years of regulatory and industry experience covering the full scope of IVD products."

BSI is working with two of the world-leading test laboratories – Paul Ehrlich Institut in Germany and Sanquin in the Netherlands – to provide Annex II List A Verification of Manufactured Product Testing. Companies using these laboratories that choose to transfer to BSI can keep their same testing facilities which will enable a smoother and more seamless transition.

Gary Slack, Commercial Director, BSI Healthcare adds, "In the near future we will be offering a series of dynamic and informative complimentary IVD webinars along with more formal training courses, ranging from beginner to advanced. We have developed an excellent programme that is designed to meet the regulatory demands of this exciting marketplace, both now and in the future.

About BSI

BSI Group is a global independent business services organization that inspires confidence and delivers assurance to over 80,000 customers with standards-based solutions. Originating as the world’s first national standards body, BSI has over 2,500 staff operating in over 140 countries through more than 50 global offices. BSI’s key offerings are:

  • The development and sale of private, national and international standards and supporting information that promote and share best practice
  • Second and third-party management systems assessment and certification in all critical areas of management disciplines
  • Testing and certification of services and products for Kitemark® and CE marking to UK, European and international standards. BSI is a Notified Body for 15 New Approach EU Directives
  • Certification of high-risk, complex medical devices
  • Performance management software solutions
  • Supply chain security solutions which identify and mitigate risks in supply chains
  • Training services in support of standards implementation and business best practice.

BSI and Kitemark were both voted UK Business Superbrands in 2010, by independent brand experts.