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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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Designed by CK and
DLC