CE Marking Certification helps everyone for existence of business globally:
CE Mark full form is Conformite Europeenne & it means that since 1985 European Union’s Mandatory conformity marking has to regulate the all process of goods that has to be sold within European Economic Area (EEA).

For All the medical devices that you want to sale in 32 European countries, for this, it is necessary for you to first obtain CE Marking Notified certification for your products. CE Marking represents that your medical products such as PPE Kit, Sterilize Machine, and Thermometer and so on are maintaining regulatory compliance & all components are secure.

CE Marking Notified Certification offices in Europe & their regulatory experts help the companies to obtain CE Marking to start selling their products in the European countries.

Why we need CE Marking Certifications:
The companies these days need CE Marking Certifications, especially those, who want to sell their products worldwide. Moreover, these notified certifications represent the conformity that all the medical products that they are sold within the European Economic Area (EEA) are offered proper health, safety, environmental protection. So before selling any products in any European country, everyone must take approval from CE Marking Notified Certifications.

Why you pick up the notified certification services from ISO Quality Consultant:
This consultant always help the small business owners & startups companies are to provide CE Marking Notified Certifications that helps them to flourish their business globally. Our professional services allow them, our clients to sell their products, in 32 European countries.

ISO Quality Consultant is one of the leading companies that help the clients to provide notified certifications that belong to a wide variety of industries.
We always ready to deliver effective solutions to our clients that help to meet the comprehensive requirements of notified certifications. Our Company has to take proper responsibility to take certification from European countries for the sale of goods of our clients there. We take certifications for our clients that help them to the transmission of medical devices to foreign countries with safety & proper regulations.

Now question arises how you can CE Marking Certifications:

• Firstly, to get approval from CE Marking, it is essential that your all medicinal products must be meeting according to the specific standards such as performance, quality, safety & efficacy of type of product you want to sale there in European countries.
• You have to obtain ISO CE Marking Certificates from the notified body before sale of any products in European Countries.

It is important to know, how long this CE Marking certification is valid:
According to rules and policies, the CE certificates that are granted by notified bodies have to be valid for approximately a period of three years. In some cases notification period is of one year only for some high risk devices. CE certification status has to depend on how much you have to maintaining of your quality system certification.

To who will issue you CE Marking Certificate?
All the medical devices that falls under category of Class I require the certification from notified body. Else Class-I non–measuring devices do not need any type of self certification from the notified body.

Is the notified body name will appear on your product labeling?
Yes the four digits notified body number will display under the labeling of your CE Marl symbol.

What is the value of CE Marking on our medicine products?
There is value of CE Marking on your label products, and this certification has to reduce the risk of selling products in Europeans countries. It also helps to make identity of products and makes the presence of your genuine products worldwide.

Auditor / Trainer

ISO Consultant