Organisational Setup of FSL | Budding Forensic Expert

Budding Forensic Expert
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 Organisational Setup of FSL 


1. Personnel:


(I) Director


(II) Reporting Officers 

  • Chemistry and Explosive   

  • Toxicology 

  • Biology and Serology 

  • DNA Fingerprinting 

  • Physics 

  • Ballistics 

  • Questioned Document 

  • Forensic Psychology 

  • Fingerprinting 

  • Crime Scene Investigation 

(III) Supporting and Non-Testifying Staffs


2. Training and Development:

A training program must develop and design for each functional area of the Laboratory 

3. Evidence Management 


4. Documentation 


 (I) Method Validation:

  • Homogeneity of Sample 

  • Concentration Range 

  • Matrix defect (if any) 

  • Interference 

  • Specificity 

  • Stability of measured Compounds 

  • Linearity Range 

  • Population Distribution 

  • Precision

(II)  Reference Material 


5. Quality Assurance 

(I) Quality Control  

(II) Reference Collection 


 6. Proficiency Testing:

The Laboratory must have documented its Policies and Procedures for…

  • Case Record Review 

  • Court Testimony Monitoring 

  • Corrective and Preventive Actions

 7. Instruments and Equipment

  •  Name of the instrument/equipment,

  •  The manufacturer's name, type, identification and serial number or other unique identification,

  •  Date received and date placed in service, where appropriate

  •  Current location, where appropriate

  •  Condition when received (for example, new, reconditioned), where appropriate.

8. Calibration

  • Instruments/Equipment 

  • Chemical Analysis

9. Quality Check


10. Reports


  • A title (e.g. test certificate, test report)

  •  The date of issue of the report

  •  The name and address of the laboratory and if different from the address, the location where tests were performed

  •  Unique identification number of the report (e.g. by report number) on each page

  •  The page number and the total number of pages (i.e. page ‘x’ of ‘y’) on each page

  •  The name and address of the client

  •  Description, unambiguous identification and date of receipt of the item(s) tested or examined

  •  Date of performance of the test and or examination

  •  Identification of the test/examination method or procedure

  •  Test/examination result

  •  Reference to sampling procedure used by the laboratory where these are relevant to the validity or application results

  •  Reference to other information where this may be relevant to the validity or application of results

  •  The name, title and signature or equivalent identification of the person authorised to release the report

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