If the medical device is manufactured outside of the European Union, the CE marking provides access to European markets for products. Before putting the product on the market in the European Economic Area, the manufacturer shall be required to get and display the CE mark on the product (EEA). This responsibility shifts to the importer if the medical device is brought in from outside the EEA. The abbreviation “CE” stands for “European Conformity,” which is the English translation of the French word “Conformité Européene.
Since ISO 13485 is in line with European medical device directives, putting it into practise aids in meeting their requirements. As a CE mark medical device consultant , we provide guidance to medical device manufacturer for the proper and valid ISO13485 standard certification.
Important steps for getting CE marking on your Medical Device:
Getting the CE marking on your device involves some logical and formal procedures. The “old technique” demanded that incredibly stringent technical requirements be met. The following steps will be useful as you move through the “new way,” which includes more fair and standard requirements for safety and functionality:
- Identify medical device status:
- Recognize regulatory requirements and their fulfil-ment:
- Development and preservation of the technical files:
- Review for product conformity:
- Declaration of conformity:
As medical device regulatory consultant we assured that, Companies operating outside of the European market that already have a Quality Management System based on ISO 13485 standard can more easily obtain the CE mark for their products because the ISO 13485 standard already satisfies many of the directives’ requirements for conformity assessment evaluation. In some instances, a manufacturer’s certificate of declaration of conformity is sufficient to get a CE mark for medical devices produced using ISO 13485-compliant systems.
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Phone no - 93702 83428
Mail id – enquiry@operonstrategist.com
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Phone no - 93702 83428
Mail id – enquiry@operonstrategist.com
If You Want Medical Devices Services Consultation For Following.- Medical Device Consulting
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- Primary Packaging Turnkey Project Consultant
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- Medical Device Compliance & Regulatory Services
- Cdsco India authorized agent for medical device
- Medical Device Consulting
- cdsco registration
- FDA 510k Clearance
- ce mark medical device
- CDSCO Manufacturing License
- CDSCO import license
- TURNKEY PROJECT CONSULTANT
- medical device manufacturing
- iso 15378 certification
- 21 cfr part 210 and 211
- ISO 13485 Medical Device Consultant
- Primary Packaging Turnkey Project Consultant
- Clean Room Design Consultant
- manufacturing site conceptualization
- Market Analysis and feasibility for Medical Devices
- manufacturing plant layout design
- medical device design and development
- DMF file submission guideline
- 21 cfr part 820
- qms certification services
- capa management
- design control requirements
- medical device process validation
- combination product
- continuous improvement program
- Medical Device Compliance & Regulatory Services
- Cdsco India authorized agent for medical device
