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
Costco Supplier Requirements
Costco Supplier Requirements All facilities that are involved in processing, packing, warehousing, or distributing consumable products or supplying food-contact packaging materials to Costco Wholesale Corporation…
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
Food Safety Culture
What is Food Safety Culture? Food Safety Culture refers to the collective attitudes, beliefs, and behaviors related to food safety within an organization. It is…
Sector
Aerospace
Aerospace Confidence and trust in the aerospace industry is vital for the success of businesses operating within this sector. Given the critical nature of aerospace…
Standards & Schemes
SQF Food Safety and Quality Codes
SQF Food Safety and Quality Codes The SQF Program is recognized by the Global Food Safety Initiative (GFSI), which is a globally recognized benchmark for…
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…