

Your trusted partner in achieving CE marking compliance. CE marking is a required conformity mark for products sold in the European Economic Area (EEA), signifying adherence to EU regulations and directives on health, safety, and environmental protection.
CE marking is a mandatory conformity marking for products sold within the European Economic Area (EEA), indicating compliance with EU regulations and directives regarding safety, health, and environmental protection.
Product Assessment and Classification: We begin by assessing your products to determine their classification and identify applicable EU regulations and directives. This assessment helps us develop a customized compliance strategy tailored to the specific requirements of your products.
Documentation Preparation: We assist in preparing the necessary documentation, including technical files, declarations of conformity, and risk assessments, required for CE marking compliance.
Post-Market Surveillance: We provide support for post-market surveillance activities, including monitoring product performance, handling complaints, and reporting adverse events to regulatory authorities.
CE marking compliance offers numerous advantages for businesses seeking to access the European market. It signifies that products meet the rigorous safety, health, and environmental protection standards required within the European Economic Area (EEA).
Our ISO certification process begins with a comprehensive assessment to identify gaps, followed by tailored documentation and implementation of necessary changes. We conduct internal audits, coordinate the external certification audit, and continue to support your organization for continual improvement post-certification.
Call US
Email Documents
Make Online Payment
Get ISO Certificate
Our Online ISO Certificate offer comprehensive support, including assessment, documentation, and implementation tailored to your organization's needs. We conduct internal audits, coordinate external certification, and provide ongoing support for continual improvement post-certification.
The documents needed for ISO certification may vary depending on the specific ISO standard an organization is pursuing (e.g., ISO 9001 for quality management, ISO 14001 for environmental management, ISO 27001 for information security management, etc.). Nevertheless, certain key documents are generally required across most ISO certifications.
Quality Manual: This document details the organization's quality management system (QMS), covering its scope, objectives, and procedures to ensure compliance with the relevant ISO standard requirements.
Quality Policy: A formal statement from top management that demonstrates the organization's commitment to quality and adherence to the ISO standard.
Documented Information: Records of various activities and processes, such as forms, reports, contracts, and other pertinent documents.
At Online ISO Certificate, we deliver thorough support, including assessments, documentation, and implementation tailored to your organization’s specific needs. We conduct internal audits, manage external certification processes, and offer continued support to drive ongoing improvement after certification.