ISO 13408-4 specifies general requirements for cleaning-in-place (CIP) processes applied aseptically to product contact surfaces of equipment used in the manufacture of sterile healthcare products and provides guidance on qualification, verification, operation and control.
ISO 13408-4 is applicable to processes in which cleaning agents are introduced into product-contact interior surfaces of equipment designed to comply with CIP. ISO 13408-4 does not apply to processes where equipment is disassembled and cleaned in a washer.
ISO 13408-4 does not replace or replace national regulatory requirements such as good manufacturing practices (GMPs) or supplementary requirements of certain national or regional jurisdictions.
EUROLAB assists manufacturers with ISO 13408-4 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.
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EUROLABreporting and certification activities, United Accreditation Foundation (UAF), Turkish Accreditation Agency (TÜRKAK) ve Enterprise Accreditation Foundation (EAF) based on the accreditation provided by the accreditation body. The Enterprise Accreditation Foundation (EAF) accreditation body is also a signatory of the United Nations (UN GLOBAL COMPACT) organization.
