ITAR Certification
EMLinQ LLC is pleased to announce it has received approval of the ITAR Registration. The International Traffic in Arms Regulations (ITAR) controls products, technologies and sevices designated as a defense article under the U.S Munitions List, as well as inherntly military technologies. Companies involved in the manufacture, sale or distribution of ITAR controlled goods or services must be "ITAR compliant"
ISO 9001:2015 Certification
EMLinQ LLC is pleased to announce it has received ISO 9001:2015 certification. The International Organization for Standardization (ISO) established ISO 9001:2015 as a family of standards that state generic requirements for instituting a company's quality management system.
ISO is a network of the national standards institutes of 147 countries, on the basis of one member per country, with headquarters in Geneva, Switzerland. The ISO standards adopted by this non-governmental organization are universally recognized and accepted. ISO 9000 certification is voluntarily pursued by companies, such as EMLinQ LLC, desiring to continually improve their quality.
AS 9100:2015 Rev D Certification
EMLinQ LLC is proud to announce the successful completion of AS9100 registration, which is the international aerospace quality standard.
The addition of AS9100 Certification complements EMLinQ's ISO 9001:2015, UL and ITAR Certifications and highlights the company's focus on supporting the stringent requirements of the aerospace, aviation, and defense industries.
AS9100 is published by the Society of Automotive Engineers, based on the ISO 9001:2015 quality management standard, and provides 80 additional requirements and 18 amplifications specific to aerospace business operations. Additional requirements necessary to fulfill AS9100 compliance include: supplementary traceability requirements, greater controls for changes to production processes and equipment, considerations for detection of contaminations or damage, and defined requirements for non-conforming material control. The standard also ensures comprehensive supplier controls as well as stringent systems for production planning and identification of "Key Characteristics and Risk Management."
FDA21: PART820
Manufacturers must establish and follow quality systems to help ensure that their products consistently meet applicable requirements and specifications. The quality systems for FDA-regulated products (food, drugs, biologics, and devices) are known as current good manufacturing practices (CGMP’s).
CGMP requirements for devices in part 820 (21 CFR part 820) were first authorized by section 520(f) of the Federal Food, Drug, and Cosmetic Act (the act). Under section 520(f) of the act, FDA issued a final rule in the Federal Register of July 21, 1978 (43 FR 31 508), prescribing CGMP requirements for medical devices. This regulation became effective on December 18, 1978, and was codified under part 820.
UL Z193 Certification
UL stands for Underwriter Laboratories, a third-party certification company that’s been around for over a century. UL was founded in 1894 in Chicago. They certify products with the aim to make the world a safer place for both workers and consumers. Besides testing, they set industry standards to follow when innovating new products. Last year alone, about 14 billion products with the UL seal entered the global marketplace.
In a nutshell, UL is a safety organization that sets industry-wide standards on new products. They continually check these products to ensure they’re up to these standards. UL testing makes sure that wire sizes are correct or devices can handle the amount of current they claim to be able to. They also ensure that products are constructed correctly for the highest safety.