CDH an ISO 9001 : 2015, ISO 14001:2015, ISO 45001:2018 certified company in accordance with the Quality Management System, a quality manual and inspection documents define the processes and activities of our organisation. We periodically monitor our services and performance to constantly improve and update ourselves. We are committed to manufacture products as per International Standards for total customer satisfaction, achieved by our dedicated teamwork.
GMP is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product. CE & ISO 13485:2016 marking on a product indicates that the product complies with and has satisfied the essential requirements set out by the In Vitro Diagnostic (IVD) Medical Devices Directive 98/79/EC, it also demonstrates the fact that the product is fit for its intended purpose.
