Laboratory Sciences
Why Choose PHCR-Europe LS, an Accredited Biological and Environmental Testing Laboratory? 
When selecting a laboratory to fulfill your analytical requirements, you need to be sure the laboratory can provide accurate, precise, timely and reliable data. One way to ensure that laboratory's ability is to look for one that is accredited to the ISO /IEC 17025 international standard.

A technically competent laboratory will have all of the elements listed below fully developed in its Quality System.

Document Control

  • All PHCR-Europe LS employees perform work using ONLY current approved Standard Operating Procedures (SOPs) based upon the most recent reference methods.
  • This eliminates "out of specification" work and helps to ensure reproducible analytical results.
  • Minimizes confusion and helps to prevent errors.
  • Requires an organized system of communication, training, and record keeping, all of which are hallmarks of a well run laboratory.

Controlled Data

  • All PHCR-Europe LS data is reviewed for accuracy by qualified experts before release to the customer. This eliminates unnecessary concern, review and time on the part of the customer.
  • Data is periodically reviewed through internal and external audits to ensure quality and conformance to SOPs.

Procurement Control Program

  • All supplies must be provided by management approved vendors, preference is given to vendors who are registered to ISO 9001:2008 and/or ISO 14001:2004. This ensures that all suppliers meet strict requirements for excellence.

Disaster Recovery Program

  • PHCR-Europe LS maintains Traceable Measurement and Test Equipment, computers and peripherals. To ensure mission essential equipment operates at optimal performance, PHCR-Europe LS maintains comprehensive manufacturer service contracts. It is LS’ assurance of timely and accurate customer data as agreed
  • All equipment failures are thoroughly investigated to determine the extent of impact, if any, the failure had on customer data. Prompt customer notification is performed when necessary.
  • All electronic data is secured through at least three levels (minimal) of data storage: copied from the instrument to a RAID-5 NAS system, all data is backed up daily via Digital Linear Tape (DLT) and stored in a fireproof safe at an offsite facility, and DVD format of each data file is copied to and stored in an offsite fireproof safe in a secured environment.

Measurement and Test Equipment Traceability

  • PHCR-Europe LS equipment and instrumentation is installed by the manufacturer and certified prior to use.
  • Whenever possible, all instrumentation and equipment is calibrated by independent third party accredited vendors annually to ensure traceability to a national standard.
  • Whenever possible, calibration standards are traceable to the National Institute of Standards and Testing (NIST) or equivalent national standard.
  • All instrument repair documentation is maintained.
  • Complete historical equipment function verification / preventive maintenance logs are maintained for each item of measurement and test equipment.

Quality Assurance Program

  • The PHCR-Europe LS Quality Assurance Division manages an intensive internal audit program of all laboratory operations to ensure compliance with ISO 17025:2005, ISO 9001:2008, ISO 14001:2004, and the ISO 17025:2005 National Lead Laboratory Accreditation Program (NLLAP) requirements.
  • PHCR-Europe LS Quality Assurance Division is open to all LS’ customers for laboratory audits or to ensure compliance with PHCR-Europe LS’ Quality System requirements.
  • The PHCR-Europe LS Customer Guide, LS Biologicals Submission Guide (BSG), Table 1 (Analytes, Methods, & Limits), and LS Price List, are available to customers as uncontrolled copies of these documents in Adobe Acrobat PDF format.
  • Customer comments are appreciated and are regularly solicited through the use of Customer Satisfaction surveys.

Comprehensive Training Program

  • All PHCR-Europe LS employees receive ongoing training in Quality Assurance Procedures, Standard Operating Procedures, Internal Audits, Safety, and Ethics.
  • All technical staff of the PHCR-Europe LS Team participate in a comprehensive training program and must demonstrate expertise in the performance of analytical procedures and the LS Quality System before they may be granted Approved Signatory status. This is followed by a mandatory supervised 3 or 6 month working period.
  • Training records are available to customers for review upon request.

Environmental Health and Safety Program

  • THE PHCR-Europe LS Chemical Hygiene Plan is available to customers upon request.
  • All PHCR-Europe LS employees are trained in required Health and Safety practices.
  • PHCR-Europe LS adheres to all U.S. Army safety rules, and participates in U.S. Army Safety Training programs.
  • PHCR-Europe LS ensures compliance with all applicable Federal health and safety requirements and the International Standards for Environmental Management Systems (EMS) described by ISO 14001:2004. It also meets the criteria of Executive Order 13148, Greening the Government through Leadership in Environmental Management, and DOE Order 450.1, the Environmental Protection Program, that require Federal facilities to implement EMSs, as well as the Code of Environmental Management Principles for Federal Facilities.

Technical Development and Support Program

  • PHCR-Europe LS provides timely support to personnel deployed or stationed throughout Europe, the Middle East, Southwest Asia and Africa.
  • PHCR-Europe LS analytical procedure improvements and revisions undergo third party validation.
  • Third party validation studies are available to customers upon request.
  • All PHCR-Europe LS Test procedures meet and/or exceed the requirements of ISO 17025.
  • Measurement Uncertainty Data is collected on a routine basis from all analytical procedures (where applicable) and is available its customers upon request.

Mutual Recognition Program

  • Nationally recognized accreditation bodies realize that they operate in an equivalent way and that they deliver equivalent accreditations that provide the same level of competence and confidence throughout the world. A test, inspection report, or a certificate issued by an accredited body in one country is recognized as equivalent to a report or a certificate issued by an accredited body in any of the countries that are signatories to the MLA.
  • Accreditation bodies certify equivalent laboratory and quality management operations and therefore the ability provide the same level high of competence and confidence.
  • The MLA makes accreditation a "passport" which facilitates access to the international markets through co-operation with ILAC (International Laboratory Accreditation Co-operation), International Accreditation Forum (IAF) and the European Co-operation for Accreditation (EA).