Thursday, 15 November 2018

What is visual inspection


visual inspection banner

Visual Inspection, used in maintenance of facilities, mean inspection of equipment and structures using either or all of raw human senses such as vision, hearing, touch and smell and/or any non-specialized inspection equipment.

 

Scope: Final visual inspection is performed manually by human operators.

Prior to being qualified as an inspector, each inspector must be successfully trained and qualified per this procedure.


Qualification Criteria



  • Inspectors are qualified if their detection of rejects is ≥ 70% detection of known rejects and ≤ 30% of blanks (false reject) in any given test set.

  • The inspector must meet this requirement three (3) times before being considered a qualified manual visual inspector

Re-Qualification Schedule



  1.  Visual inspectors are re-qualified annually.

  2. If inspection performance declines, re-qualification may be required in shorter time-frames.

  3. Annual eye sight exams at optometrist for visual acuity with 20/20 vision or 20/20 corrected. If eyesight is corrected with eye glasses or contact lenses, then those must be worn during the product inspection process.

References:.




  1. Injections and Implanted Drug Products (Parental) – Product Quality Tests

  2. Visible Particulates in Injections 3.    USP Visual Inspection of Injections


Responsibilities:



  1. It is the responsibility of the Production Manager/Production Officer to ensure that visual inspectors are qualified per this SOP.

  2. It is the responsibility of the Quality Assurance (QA) to perform investigations of inspectors who do not meet re qualification requirements.

Procedure:


The inspection process is designed to ensure that 100% of every container Of every lot of parental preparations is “essentially free” from visible particulates.

  1. Different test sets needed for each drug product category.


  • Clear Liquid

  • Suspension

  • Others


  1. The test sets can be made up of production rejects or created manually with Characterized particulate material.  Test sets are made up of blank ampule with particles/fiber Misprinted Sealing defect

  2. Test sets are labeled so as to keep the identity of the rejects unknown to the trainee.

  3. Units that are no longer usable in a test set due to breakage, particle no longer detectable; cake breakage, etc. will be replaced.


Qualify an inspector using a test set that is representative of the product to be inspected.  For example, if the product to be inspected contains gel, qualify the inspector using the test set containing gel.




  1. Inspectors are qualified if their detection of rejects is ≥ 70% detection of known rejects and ≤ 30% of blanks (false reject) in any given test set. The inspector must meet this requirement three (3) times before being consider a qualify manual visual inspector.

  2. The trainee is train on the operation of the manual inspection booth.

  3. The trainee is shown the rejects within the test set to be train upon. Each of the rejects is describe as the trainee inspects the rejects within the test set. A blank is also give for inspection as well.

  4. Ensure that operators spend appropriate time (5+ seconds against each color background) with each product container during the visual inspection process

  5. The reject vials are then mix in with the rest of the test set and the trainee inspects each vial while being observe by the trainer.  The trainee inspects all of the vials and notes the defect code for the reject vials while maintaining separation of the rejects and the blanks.

  6. Upon completion the trainer compares the trainee’s determinations to the actual defects/blanks. ≥ 70% detection of know rejects and ≤ 30% of blanks (false reject) is required to pass.  The trainee repeats the inspection process until successfully passing three (3) times


Inspector Re-Qualification Schedule:




  1. Visual inspectors are re-qualify annually.

  2. If inspection performance declines, re-qualification may be required in shorter time-frames.

  3. Common causes of declined performance that may lead to a need for re-qualification include fatigue, demonstration of an improper reject rate during operations, etc. and/or causing excessive product investigations

  4. Annual eye sight exams at optometrist for visual acuity with 20/20 vision or 20/20 correct.  If eyesight is correct with eye glasses or contact lenses, then those must be worn during the product inspection process.

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