Medical Devices
Medical devices are instruments, equipment, implants, or software used in the diagnosis, treatment, or prevention of medical conditions
he regulatory requirements for the medical devices industry have become more complex in recent years, primarily aimed at ensuring patient safety and protecting the end consumer.
Meet Regulatory Requirements While Protecting Consumers Safety
Meeting regulatory requirements and protecting consumer safety are critical objectives for the medical devices industry
Related Services
In addition to the services mentioned earlier, there are several related services that can further support improving business excellence maturity and sustainable business practices. These services include:
Standards & Schemes
ISO 9001 Quality Management Systems
ISO 9001 Quality Management Systems ISO 9001 provides a robust framework that can be tailored to any industry or sector. It offers a systematic and…
Training
Assurance Training The primary purpose of assurance training is to enable individuals to assess, evaluate, and provide independent assurance on the effectiveness of controls, processes,…
Standards & Schemes
Medical Device Single Audit Program (MDSAP)
Medical Device Single Audit Program (MDSAP) The Medical Device Single Audit Program (MDSAP) is designed and developed to cover relevant requirements from the Regulatory Authorities…
Standards & Schemes
ISO 45001 Occupational Health and Safety Management System
ISO 45001 Occupational Health and Safety Management System ISO 45001 is an international standard that specifies the requirements for an occupational health and safety management…