As their companies progress to operate under a single quality framework with a common set of quality and compliance elements, these actions help to make sure the highest quality products on which their customers have relied for more than a century, continue to be available. Each Johnson & Johnson operating company is expected to make sure that:
Products meet safety and quality requirements and perform as required throughout their shelf life
All products and ingredients they purchase from suppliers meet their requirements
Changes to materials, product labeling, packaging, processes, systems, facilities, methods and equipment are reviewed and approved before they are made
Procedures are in place to prevent diversion of their products from their intended distribution channels and to protect them from counterfeiting (Johnson & Johnson, 2012).
Their companies work closely with health authorities, various standard setting bodies, and professional organizations worldwide to be sure their quality systems are up-to-date and are continuously improving. Many of their businesses and facilities have been certified to meet International Organization for Standardization (ISO) requirements for quality management. ISO certification means that a quality management system has been thoroughly reviewed by an outside audit committee and found to satisfy rigorous standards. All of their facilities that make medicines or medical devices meet current Good Manufacturing Practices (cGMP), as outlined by the FDA or one or more other national regulatory agencies. Training programs at the companies give employees the necessary tools to create and manage quality systems that ensure our products perform as intended and meet all regulatory requirements (Johnson & Johnson, 2012).
Their commitment to compliance extends to their external manufacturers who they rely on to produce ingredients as well as finished goods. The Johnson & Johnson Responsibility Standards for Suppliers helps them identify and select partners who operate...
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