Rudolph Research Analytical maintains a philosophy of continuous improvement and growth by developing products that are innovative and of the highest quality while conducting itself with integrity in all aspects of its business. Integrity, Quality and Innovation anchored upon Biblical Principles forms the foundation of our company.
Laboratory personnel who perform calibration of Quartz Control Plates are familiar with the quality documentation, which is implemented in their work, policies and procedures. Rudolph Research Analytical provides copies of the quality documentation to the laboratory staff and/or informs the staff of its location. Laboratory staff reviews the documentation as part of their training, which is recorded in their training records.
NVLAP - Stands for National Voluntary Laboratory Accreditation Program
The National Voluntary Accreditation Program operates as an independent third party whose purpose is to accredit testing and calibration laboratories. National Institute of Standards and Technology, NIST Handbook 150 sets forth the procedures and requirements a laboratory must meet to be accredited. Under the NVLAP program a laboratory must demonstrate that they operate an appropriate management system, are technically competent, and are able to generate technically valid results.
The program provides an unbiased third-party evaluation and recognition of performance, as well as technical competence.
Download the NIST 150 Handbook here »
Benefits include Market Advantage, Consistency of Operations, Increased Awareness, and Process Improvement
International standards-based accreditation programs, such as NVLAP, rely on a uniform recognized approach to determine competence, promote mutual recognition among accrediting bodies, and support increased acceptance of export goods in international markets. NVLAP, because of its close working relationship with the NIST laboratories, is widely recognized and respected as a technically sound and rigorous accreditation program.
Customers respect an independently administered, internationally recognized accreditation program provides a more organized operating environment and constancy across their suppliers. This is especially true in the Pharmaceutical industry.
All others being equal, an accredited laboratory will obtain the business before non-accredited laboratory.
A company's QMS defines the organization's policies, procedures and internal requirements that ensure customer requirements, regulatory and industry requirements are consistently met, resulting in customer satisfaction and reduce organizational risk.
The QMS include:
An effective Quality Management Systems will define the critical processes, set system controls, monitor performance of its processes and demonstrate continual improvement.