What is CE Certification?
The CE Mark is a mandatory conformity marking in the European Union (EU) that has been in place since 1985 to regulate goods sold within the European Economic Area (EEA). It signifies that a manufacturer has declared their product’s compliance with the EU’s New Approach Directives, which apply not only to products within the EU but also those intended for sale or manufacture in the EEA. As a result, the CE marking is recognizable globally, even to those unfamiliar with the EEA.
Rietway Consultants CE Certification Package
The Services which are included in our package are as Follows:
✅ Consultation for CE Certification
✅ Preparation of Documents
✅Application Filing
✅CE Certificate
Documents Required for GMP
1. Business Registration Proof
2. KYC of Proprietor/Partners/Directors
3. Objectives of Business
4. Email Id and Phone Number
5. Current Electricity Bill
CE Procedure
Step -1 Arrange all Required Documents: The first step is to arrange all the documents and send the same over the email / WhatsApp to us. Once all the Documents are Received, we will Start the Further Process.
Step2: Preparation of Documents: The Next Step is Preparation of Documents to be Submitted at Department.
Step-3 : Filling Of Application For CE : The next Step is Filling Of Application for CE.
Step4: After approval of the application Department Issues CE Certificate.
Benefits of CE Certification
– Fulfills the requirements of relevant European product directives.
– Meets all the requirements of the relevant recognized European harmonized performance and safety standards.
– Is fit for its purpose and will not endanger lives or property.
Types of CE marking
Manufacturer or authorised representative of the product affixes CE marking to the product.
CE marking is given when the product successfully meets all the CE requirements.
Minimal Risks
A minimal risk product requires a self-declaration along with the Declaration of Conformity from the hand of the manufacturer for affixing CE marking to their product.
Greater Risks
The EU’s New Approach Directives mandate that products with a higher degree of risk should be certified by a notified body, which is designated by the European Commission. The notified body collects all the necessary information to ensure compliance with the directives. Notified bodies can be either private organizations or government agencies.
FAQ on CE Certification
Q1. What does CE Stands For?
CE stands for European Conformity. This certification works as a proof of mark affixed on the product which reflects health, safety and climate protection standards of products sold within the European Economic Area (EEA).
Q2. What are the Elements of CE Certification?
CE stands for European Conformity. This certification works as a proof of mark affixed on the product which reflects health, safety and climate protection standards of products sold within the European Economic Area (EEA).
Q3. What is Declaration of Conformity?
This document states the essential health and safety requirements of the relevant legislation of the product. The creation and signing of this document also state that the manufacturer assumes responsibility for the CE marketing compliance of the product.
Q4. What is the Validity of CE certification?
Each certificate is valid for a period of 3 years from the date of issue.