ISO 22716, Cosmetics Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and ISO 13485 Medical Devices Certification
ISOsafe help Medical, Pharmaceutical and Cosmetic companies to comply with Good Manufacturing Processes - ISO 22716, Good Distribution Practices (GDP) and Medical Devices Quality Management - ISO 13485.
ISO 22716 - Good Manufacturing Processes - GMP
Cosmetic Companies may require ISO 22716 to comply with GMP Guidelines for production, control, storage and shipment of their products.
ISO 22716 increases customer confidence and improves consumer safety, furthermore the framework assists with regulatory and contractual compliance.
An effective GMP framework ensure suppliers (and any subcontract manufacturers) are meeting their obligations thereby enhancing customer satisfaction.
Why work with ISOsafe? Only experienced professionals can help your business to become a safer manufacturer of cosmetics.
Trusted ISO 22716 GMP systems from ISOsafe safeguard your business’ success. We can help your business with compliance, training, audits and certification, Call ISOsafe now 1300 789 132
Good Distribution Practices - GDP
Is your business a Distributor only? Youll need a Good Distribution Practice (GDP) framework. GDP typically required by Pharmaceutical, Transport and Logistics Companies.
GDP guidelines set out the minimum standards that a wholesale distributor must meet to ensure that the quality and integrity of medicines is maintained throughout the supply chain.
The Department of Health and Aged Care, Therapeutic Goods Administration (TGA) sets out the Australian code of good wholesaling practice for medicines in schedules 2, 3, 4 & 8 – more information can be accessed here: Australian code of good wholesaling practice for medicines in schedules 2, 3, 4 & 8.
Feeling overwhelmed? Call ISOsafe to get ISO 22716, GMP or GDP compliant today.
ISO 13485 - Medical Devices Quality Management
Are you seeking ISO 13485 Certification? ISOsafe specialises in Medical Device Quality Management Systems. We can prepare a custom Quality Management System to help your business comply with ISO 13485 Medical Devices.
ISO 13485:2016 Quality Management for Medical Devices sets out the requirements for a quality management system where an organisation needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements.
Organisations that adopt ISO 13485 ensure they showcase their commitment to Safety, as well as, comply with their regulatory and contractual obligations.