ISO 13485
ISO 13485 is an international standard for medical device design and development which specifies requirements for a comprehensive quality management system in order to ensure that products conform to customer and regulatory requirements. In other words, ISO 13485 is a quality management system standard that was specifically created for the medical device industry. It helps companies ensure that their products are safe and compliant with regulations.

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GMP CERTIFICATION
Good Manufacturing Practices (GMP) helps organizations to develop products in line with specific standards that ensure product quality and safety. In CGMP, the letter ‘c’ means current and it was added to say that the manufacturer/supplier should follow the current technologies and system processes.

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ISO TRAINING
ISO training is for individuals who are interested in learning more about ISO management systems and how to implement them within organizations to achieve ISO certification. Additionally, ISO training can help you gain knowledge on how to conduct internal and external audits of an ISO management system.

https://iasiso-middleeast.com/JO/iso-training/