Certificates

	CE The CE marking is a certification indicating that a product complies with the essential requirements of relevant European Union (EU) directives and regulations, ensuring its safety, health, and enivronmental standards.

	GMP Good Manufacturing Practice (GMP) certification ensures that pharmaceutical products are consistently produced and controlled according to quality standards. It encompasses manufacturing processes, quality management systems, and adherence to regulatory requirements.
	ISO ISO (International Organization for Standardization) certification signifies compliance with internationally recognized standards for various aspects, such as quality management, environmental management, information security, and more. It demonstrates an organization's commitment to meeting specific criteria and ensuring continual improvement in its processes.
	Ministry of Health, Welfare and Sport The Ministry of Health, Welfare and Sport is the Dutch Ministry responsible for public health, health care, quality of life, social work and sport.
	State Food and Drug Administration The National Medical Products Administration (NMPA) is China's regulatory authority responsible for ensuring the safety and quality of food, pharmaceuticals, and medical devices.
	Department of Health China Responsible for overseeing health policies and public health initiatives.
	ISO 13485:2003 ISO 13485:2003 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and related services.
	Food and Drug Administration Thailand The Thailand Food and Drug Administration (TFDA) is the national regulatory body and competent authority responsible for the registration, evaluation, and monitoring of food and drug products in Thailand.
	Health Sciences Authority The Health Sciences Authority is a statutory board under the Ministry of Health of the Government of Singapore. It is a multi-disciplinary agency responsible for applying medical, pharmaceutical, and scientific expertise to protect and advance public health and safety.
	Ministry of Health of the Russian Federation The Ministry of Health of the Russian Federation is responsible for healthcare policy and administration in Russia.
	Malaysian Medical Device Authority The Malaysian Medical Device Authority (MDA) is the regulatory body overseeing medical devices' registration, quality, and safety in Malaysia.
	Therapeutic Goods Administration Australia The Therapeutic Goods Administration (TGA) is Australia's regulatory authority responsible for assessing and regulating therapeutic goods, including pharmaceuticals and medical devices, to ensure their safety and efficacy.