Product Certification
CE Mark is a conformity mark that is mandatory
for all goods sold within the EEA.
CE Mark is a conformity mark that is mandatory for all goods sold within the European Economic Area (EEA). CE stands for “Conformité Européenne”, and this symbolizes that the products produced by the concerned organization are meeting all the requirements related to health, safety, and being environmentally friendly.
CE mark is attached to the products delivered by the concerned organizations that are sold in European Marketplaces.
CE mark aims at the following points-
When your product has a CE mark affixed, it acts as proof of your compliance with all the relevant EU requirements. It must be noted that those products that do not have a CE mark affixed to them, are not allowed to be circulated in the European markets, as per EU requirements.
Moreover, certain strict actions are taken to prohibit their sale in the concerned area. It is very important for the manufacturers and importers to undertake measures for compliance with the safety provisions, document every action, and design their processes in accordance with the provisions of the directives. Certain directives and principles have immense safety aims and objectives, but they give flexibility to the manufacturers for processes that can be executed for achieving those aims and objectives.
For instance, if you apply for more than one CE mark directive, the manufacturer can choose among themselves as per their organization’s requirements. This marking indicates the conformity with only those directives that have been applied by the manufacturer. In the case where the manufacturer does not mention the particular directives that have been applied by them, it is assumed that the CE marking is the declaration of conformity for all applicable directives.
One benefit of the ISO 9001 certification is that it is a flexible framework. It doesn’t tell a potential consumer that one way of running a business is better than any other; instead, certification verifies that a particular business meets ISO 9001’s quality management system standards. It also verifies that their method of manufacturing a product or providing a service has been designed to ensure a high-quality outcome for the customer.
ISO 9001 sets the international standard for companies looking for ways to meet or exceed quality control metrics. At the same time, it helps consumers distinguish between companies, allowing them to make educated choices when choosing a vendor. It does this by identifying best practices for each industry, standardizing those practices and promoting adherence to those practices.
Deliver products that consistently meet customer requirements and a service that is dependable and can be relied on.
Continual improvement of processes and resulting operational efficiencies mean money saved.
Improve the perception of your organization with staff, customers and suppliers.
Understand how statutory and regulatory requirements impact your organization and its customers.
Greater consistency and traceability of products and services means problems are easier to avoid and rectify.
Independent verification against a globally recognized industry standard speaks volumes.
Understand how statutory and regulatory requirements impact your organization and its customers.
CE Mark is a conformity mark that is mandatory for all goods sold within the European Economic Area (EEA). CE stands for “Conformité Européenne”, and this symbolizes that the products produced by the concerned organization are meeting all the requirements related to health, safety, and being environmentally friendly.
Radio recurrence hardware that is sold or dispersed in the United States needs to experience testing so as to fulfill the guidelines set up CE Mark.
At the point when radio recurrence hardware experiences a testing procedure, it limits both purposeful and inadvertent electromagnetic radiations discharge from the gear to guard clients against it.
Complete a Quote Request Form so we can understand you and your business. We will then use this to personally prepare a proposal for your certification and define what is known as your 'scope of assessment'.
We will then contact you to book your assessment with an ICB assessor. This consists of two mandatory visits that form the Initial Certification Audit. Please note that you must be able to demonstrate that your management system has been operational for a minimum of three months, has been subject to a management review and a full cycle of internal audits.
Following a successful two stage audit, a decision is made and if positive, your certification is issued by ICB. You will receive both a hard and soft copy of the certificate. Certification is valid for three years and maintained through surveillance audits (years one and two,) and a recertification audit in year three.
