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ChemRight Laboratories, Inc.  QA/QC Plan is available at the lab for review by any of our customers.  Please find below the table of contents.  CRL applies strict quality assurance and quality control procedures to all the analysies we perform.  About 30% of all laboratory work is part of our  QA/QC program and each written analytical procedure contains detailed instructions and acceptance criteria for the quality control of our test results.  Attention and review of every analytical result is also part of the process we use to ensure accurate data for our customers. 

Please direct any questions regarding QA/QC at CRL to our President, David Gossman at dgossman@chemrightlabs.com.


  QA/QC PLAN TABLE OF CONTENTS
INTRODUCTION
SECTION I:  Laboratory Organization and Responsibility
SECTION II:  Instrumentation
SECTION III:  Standard Operating Procedures
SECTION IV:  Field Sampling Procedures
SECTION V:  Laboratory Sample Handling Procedures
SECTION VI:  Calibration Procedures
SECTION VII:  Analytical Procedures
SECTION VIII:  Data Reduction, Validation, Reporting, and Verification
SECTION IX:  Types of Quality Control Checks and Frequency of Their Use
SECTION X:  Preventive Maintenance Procedures
SECTION XI:  Corrective Action
SECTION XII:  Record Keeping Procedures
 
APPENDICES
Appendix I: SOPs
Appendix II: Sampling Instructions


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