Procedural # |
Title |
HIC 3-0001 |
HIC Quality Management Program |
HIC 3-0002 |
HIC Document Management Policy |
HIC 3-0003 |
How to Write an Standard Operating Procedure |
HIC 3-0004 |
HIC Records Retention and Management Policy |
HIC 3-0005 |
HIC Equipment Management Program |
HIC 3-0006 |
HIC Equipment Qualification program |
HIC 3-0007 |
HIC Training policy |
HIC 3-0008 |
HIC Laboratory Safety policy |
HIC 3-0009 |
HIC Materials Management policy |
HIC 3-0010 |
Reagent Quality Control and Inventory Policy |
HIC 3-0011 |
Antibody-Fluorochrome Management Policy |
HIC 3-0012 |
HIC Standard and Control Reagent Program |
HIC 3-0013 |
HIC Change Control Program |
HIC 3-0014 |
Bioanalytical Method Validation Program |
HIC 3-0015 |
Scientific notebook policy |
HIC 3-0016 |
Technical and Clinical Report Policy |
HIC 3-0017 |
Validation Plan, Protocol and Report Policy |
HIC 3-0018 |
Quality Control Database Management |
HIC 3-0019 |
HIC Corrective and Preventative Action Plan Program |
HIC 3-0020 |
Computer System Validation |
HIC 3-0021 |
Database management policy |
HIC 3-0022 |
HIC Website Management policy |
HIC 3-0023 |
Clinical Specimen Management Policy |
HIC 3-0024 |
Clinical Study Management Policy |
HIC 3-0025 |
Clinical Specimen Transport, Shipping, Receipt, and Distribution |
HIC 3-0026 |
HIPAA Confidentiality Policy |
HIC 3-0027 |
HIC Retest Policy for Clinical testing |
HIC 3-0028 |
HIC Laboratory Investigation Policy |
HIC 3-0029 |
HIC Phlebotomy Service Policy |
HIC 3-0030 |
International Shipping Procedure for Clinical Specimens |