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In the medical device manufacturing industry, non-conformance refers to any deviation from established quality standards and regulations. Some common types of non-conformances in the medical device manufacturing industry include: Design NCs: These occur when a device or product is not designed to meet the required specifications, regulations or standards. Manufacturing NCs: These occur...
In the pharmaceutical industry, non-conformance refers to any deviation or failure to meet regulatory requirements, quality standards, or established procedures. The following are some common types of non-conformances that can occur in the pharmaceutical industry: Deviation: Any departure from standard operating procedures, including manufacturing, testing, packaging, or labeling...
Non-Conformance and types of Non-conformances in Pharmaceutical and Medical device industries Non-conformance refers to any deviation from established quality standards and procedures in the pharmaceutical industry. Here are some common types of non-conformances that can occur in the industry: Process NCs: This occurs when a deviation from a defined manufacturing or testing process...
In this blog, we have listed the EU MDR notified bodies designated under the EU Medical Devices Regulation (MDR). We will keep this list updated as and when a new Notified Body is added.