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 13485 Medical Devices Management Systems
ISO 13485 Medical Devices Management Systems Organizations involved in the design, development, production, installation, and servicing of medical devices, as well as related services. ISO…
Assurance Terms & Conditions
Assurance Terms & Conditions Asia-Pacific Australia (UK English) Terms and Conditions for Certification, Assessment Services and TradeMark Licence Indonesia (Bahasa) Ketentuan & syarat-syarat untuk Jasa…
Audit & Certification
Ethical Sourcing
Ethical Sourcing Ethical sourcing refers to the practice of procuring goods and services from suppliers who adhere to ethical and responsible business practices. It provide…
Standards & Schemes
ISO 50001 Energy Management Systems
ISO 50001 Energy Management Systems The standard is designed to help organizations effectively manage their energy use, improve energy performance, and reduce energy consumption and…
Standards & Schemes
ISO 14001 Environmental Management Systems
ISO 14001 Environmental Management Systems ISO 14001 is an internationally recognized standard that provides a framework for organizations to establish and implement an effective environmental…