About Us
RMD was established in 2001 with a vision of marketing high quality in vitro diagnostics in the US. This vision, combined with the more than 40 years of experience of our partner organizations and exclusive dedication to immunodiagnostics, has made RMD together with its parent company the worldwide leaders in biogenic amine assays.
Why Choose RMD?
RMD is the daughter company of the manufacturer, Labor Diagnotika Nord. As such, we provide our customers with the best possible service.
We guarantee a 24-hour turnaround time on most all technical inquiries.
Quality and Reliability – LDN has developed an extensive internal Quality Assurance program and are ISO 9001-2000, and ISO 13485 Certified.
Our Mission Statement
Rocky Mountain Diagnostics is dedicated to exceeding our customers’ expectations in terms of the quality of the products and services we provide.
RMD´s mission is to:
• Maintain a quality system that meets the DIN ISO 13485 Certification Standards
• Dedicate ourselves to a strategy of continuous improvement
• Constantly seek to understand the expectations of our customers and strive to exceed those at every juncture
• Ensure that all RMD employees thoroughly understand and adhere to the spirit and the letter of the company’s quality policy, as well as the directives of the Quality Manual and its subordinate documents
Our Partners
Rocky Mountain Diagnostics is in essence the US branch of the innovative biotech company Labor Diagnostika Nord GmbH & CO KG. We represent their full product line here in the USA and Canada. Together we are a truely global operation with a distributor and OEM network in over 80 countries. LDN was founded in 1996 in Nordhorn, Germany, with the aim to develop, manufacture and supply specialty in-vitro diagnostics test systems and innovative technologies to the clinical and research laboratory markets. From the beginning the determination of Biogenic Amines with immunological test systems was the core of our business, and still is today.
LDN has developed an extensive internal Quality Assurance program and their facilities are EN ISO 9001:2008 and EN ISO 13485:2003 + AC:2009 certified. LDN participates on a regular base in national (INSTAND) and international quality assessment programs.
All in-vitro diagnostics fulfil the regulations of the new European ivd directive (CE).