How to use ISO 13485 to get your devices approved for CE Marking?

 

The CE marking is a gateway to marketing products in Europe, even if the medical device was produced somewhere other than the European Union. It is the producer’s mandatory obligation to acquire and display the CE mark on the device before marketing it in the European Economic Area (EEA). If the medical device is imported from outside the EEA, then this obligation transfers to the importer. The term “CE” is the short form of the French phrase “Conformité Européene,” which translates to “European Conformity” in English.

ISO 13485 is aligned with European medical device directives; therefore, its implementation helps to fulfill the requirements of these directives. Three different directives are applicable to different types of medical devices in Europe. Both the Medical Device Directive (93/42/EEC) and the Active Implantable Medical Devices Directive (90/385/EEC) have been modified by a new directive (2007/47/CE). The third directive is the In Vitro Diagnostics Directive (98/79/EC).

Majors steps for acquiring the CE marking on your medical device

There are some logical and procedural steps to getting the CE marking on your device. The “old method” required the fulfillment of exceedingly thorough technical conditions. The “new method” comprises more reasonable and uniform requirements for safety and functionality, and the following steps will be helpful as you work through it:

1) Identify medical device status: As a medical device manufacturer or importer in the

European market, one must identify the class of medical device needed to be marketed. Medical devices are classified according to the associated level of product risk into Class I, IIa, IIb, or III. In vitro diagnostics devices are classified into Class A or Class B.

2) Recognize regulatory requirements and their fulfillment: After the identification of medical device status, a medical device supplier or producer has to recognize the requirements of applicable EU directives and fulfill them accordingly. Some of the main areas where these requirements concentrate include:

• Suitability for intended application
• Medical device safety for the operator and the patient
• Justification that medical device benefits supersede the acceptable risks.
• Impact of transportation and warehousing of the medical device, and the justification that it does not    damage production functionality and safety
• Requirements for medical product labeling, instructions for use, and packaging

By demonstrating compliance in these areas, the manufacturer proves that the product is safe and is effective for its intended application. ISO 13485 Certification helps suppliers to achieve requirements in these areas.

3) Development and preservation of the technical files: This is also known as the technical documentation of a medical device. It comprises evidence of every manufacturing stage that shows that the product is compliant. The technical files focuses on some common areas, such as:

• Medical device components and material specifications
• Medical device product specifications
• Validation results of manufacturing processes
• Risk Management Registry of a medical device
• Design verification records for medical devices
• Design validation reports and clinical evaluation
• Labeling specifications
• Instructions for use

With the help of technical documentation and records, the manufacturer proves not only that the product is compliant with the requirements of the European Directives, but also that all the processes and phases of the manufacturing processes have been documented. ISO 13485 Certification helps to meet the above requirements through the management of medical device files.

4) Review for product conformity: The supplier or device manufacturer in Europe has to get review and approval for certain devices that fall into Class III (Active Implantable Medical Devices) and all devices in Classes A and B (in vitro diagnostics devices). Reviewers will assess the conformity of the manufacturer’s testing processes.

The type of review required before approval for the CE mark is determined by the classification of the medical device. These review paths involve the assessment of the following:

• Complete Quality Management System review
• Product design verification and validation review
• Self-declaration of conformity
• Review of Quality Management System for manufacturing
• Review of Quality Management System for product
• Review of batch release

The selection of a review path substantially influences the scope and dynamics of the review. This is the reason why correct medical device classification is very important for suppliers and manufacturers. A Quality Management System based on ISO 13485 helps to meet most of these review routes.

5) Declaration of conformity: This is the last step in which the supplier of the medical device confirms that the device fulfills all obligations identified in the relevant directives. Moreover, it declares that the device has gone through the program of conformity assessment and is manufactured, designed, and qualified as per the technical files developed. The declaration of conformity is documented on a certificate with all declaration statements of conformity.

ISO 13485 Certification helps to attain the CE mark for your medical device:

Because the conformity assessment routes include both design verification and validation review, an ISO 13485 Quality Management System for both products and processes can help manufacturers to have the required systems in place even before pursuing the CE mark for the European market.

Visit : iso 13485 UK