Elimold Manufacturing Certifications
Customer satisfaction is the primary goal of our quality management system, and we adhere to strict ISO standards and strive for continuous improvement in all our work. We have a process in place to ensure that every order adheres to the highest manufacturing standards, including tracking the performance of manufacturers in our network to ensure that orders meet our quality standards. Below is an overview of our global certifications and compliances.
Elimold Is Committed To Quality And Safety
Elimold understands that a rigorous quality management system (QMS) and accurate, comprehensive documentation are essential to providing customers with high-quality, compliant parts. Elimold Manufacturing holds multiple certifications across its global manufacturing network to ensure all parts meet stringent specifications and requirements. Elimold’s extensive certification portfolio includes ISO 9001:2015, AS 9100D, and industry certifications such as ISO 13485, ISO 14001, ISO 45001, ISO TS16949, and NIST 800-171.
ISO 9001:2015
ISO 9001:2015 is the international standard that specifies requirements for a QMS. Organizations utilizing this standard must demonstrate the ability to provide products and services that consistently meet customer and regulatory requirements. The seven principles of ISO 9001:2015 include: customer focus, leadership, engagement of people, process approach, improvement, evidence-based decision making and relationship management.
AS9100:2016
AS9100:2016 certification is an internationally recognized QMS for the Aviation, Space and Defense (ASD) sector. This QMS revision is based on the ISO 9001:2015 quality system requirements which set standards for businesses that provide design, development, production, installation and/or servicing for the ASD industry.
ISO 13485:2016
ISO 13485:2016 identifies requirements for a QMS for businesses that provide medical devices and related services to ensure customer needs and applicable regulatory requirements are consistently met. Compliant organizations can be involved in any product lifecycle stages including design and development, production, storage and distribution, installation, and/or servicing of a medical device (e.g. technical support). ISO 13485:2016 may also be required of suppliers or external vendors that provide product materials. Wherever there are outlined requirements applying to medical devices, the ISO 13485:2016 requirements apply equally to all related services as provided by the organization.
Quality Control & Certifications
In addition to ISO and AS certifications, we have several quality assurance measurements and reporting options.
- CMM Inspection Report
- Dimensional Inspection Report (DIR)
- Material Certificates + Certificate of Analysis
- REACH Certificate
- RoHS Certificate
- Certificate of Conformance (CoC)
- First Article Inspection (FAI)
- PPAP
- Conflict Minerals Reporting
- Prop65
Why Choose Elimold?
You can count on The Elimold Promise.
As an advanced technology-driven manufacturer, Elimold has an established quality policy. This policy aligns with The Elimold Promise. Elimold uniquely blends industrial 3D printing and additive technologies with traditional manufacturing driven by a differentiated customer experience focused on speed, urgency and agility.
Elimold’s quality policy sets a defined framework for overall quality objectives. These objectives outline our commitment to customer satisfaction through Elimold’s comprehensive capabilities, expertise and continuous improvement initiatives.The experts at Elimold are committed to understanding and anticipating customer needs in order to meet project requirements and exceed expectations. Start a conversation with a Elimold expert today.
Talk with a Manufacturing Expert
Want to talk more in-depth about your project and how we can partner to get the most from our manufacturing services? Connect with an experienced applications engineer for design feedback, material information, quality certifications, and more.