N. S. UNI-GLOVES SDN. BHD., a manufacturer and exporter of premium quality gloves, was incorporated in 1988. Today, after more than two decades in the industry we have expanded to producing about 850,000,000 pieces annually. 

      We believe in SAFETY THROUGH QUALITY, our motto. To ensure we live up to this motto, we practice a quality policy as below :
 

	EFFECTIVE applications of ISO9001:2008 + ISO 13485:2003.
	ENHANCE customer satisfaction.
	EFFICIENT implementation of processes.
	EVOLVE practices or processes for better efficiency and effectiveness.
	ECONOMICAL costs of production.
	ENVIRONMENT controls.

      The principal goal of the Company is to incorporate QUALITY into all our activities in order to be more efficient in controlling the basic manufacturing elements relating to product quality and production efficiency. In addition, it is also our policy to strive for continuous quality improvement to achieve better customer satisfaction. To achieve the policy, we set ourselves to focus on our customers' needs and expectations, to gain their complete confidence with honesty and sincerity. To assure our customers of our commitment to quality, we develop and implement a quality system that conforms to the ISO Quality Standard requirements and strive for continuous quality improvement and will not compromise quality in anyway. We assure our customers of our commitment, reliability and efficiency. 

Our commitment to Quality Excellence have earned endorsements from :
 

	UKAS - The United Kingdom Accreditation Service, as a medical gloves menufacturer.
	Canadian General Standards Board (CGSB).
	TÜV Product Services, Munich.
	Conforms to CE marking requirement.

	Quality Control from raw material to finished products.
	Latex and Nitrile proprietary formulation and processing.
	Latex and Nitrile glove manufacturing design and construction.
	Production flexibility.
	Investment in the newest technology.
	Environmentally Conscious.
	High Quality consistent products.
	Exceeding the ASTM, EN 455 and other Relevant Standards and Requirements.

	Stringent quality control.
	Quality "Gates" at all CRITICAL process stages - 16 inspection points.
	Validation of process performance to specification.
	Validation of data utilizing validated test method.
	Independent confirmation of performance from outside testing laboratories.
	Independent Evaluations and Endorsements.
	ISO Certification by UKAS in United Kingdom.
	CE mark Registration.
	FDA Registrations.
	CGSB (Canadian General Standards Board).
	TÜV Product Service.

	Consistent RELIABLE performance by controlling process inputs.
	Inspections gates at the factory reduce our customers "inspection time and cost".
	Traceability from raw material to finished products.
	Quality products at competitive prices translate into value to our customers.