2.0
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
- Visual inspectors are re-qualified annually.
- If inspection performance declines, re-qualification may be required in shorter time-frames.
- 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.
1. USP ,
Injections and Implanted Drug Products (Parenterals) – Product Quality Tests
2. USP Visible
Particulates in Injections
3. USP Visual
Inspection of Injections
Responsibilities:
- It is the responsibility of the Production Manager/Production Officer to ensure that visual inspectors are qualified per this SOP.
- It is the responsibility of the Quality Assurance (QA) to perform investigations of inspectors who do not meet requalification requirements.
Procedure:
A. The inspection
process is designed to ensure that 100% of every container
Of every lot of
parenteral preparations is “essentially free” from visible particulates.
1. Different test
sets needed for each drug product category.
- Clear Liquid
- Suspension
- Others
2. Test sets can
be made up of production rejects or created manually with
Characterized
particulate material. Test sets are made up of
blank ampoules,Ampoules
with particles/fiber Misprinted Sealing defect
3. Test sets are
labeled so as to keep the identity of the rejects unknown to the trainee.
4. Units that are no
longer usable in a test set due to breakage, particle no longer detectable;
cake breakage, etc. will be replaced.
B. . 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 considered a
qualified manual visual inspector.
2. The trainee is
trained on the operation of the manual inspection booth.
3. The trainee is shown
the rejects within the test set to be trained upon.
Each of the rejects is described as the trainee inspects the rejects within the test set. A blank is also given for inspection as well.
Each of the rejects is described as the trainee inspects the rejects within the test set. A blank is also given for inspection as well.
4. Ensure that operators
spend appropriate time (5+ seconds against each
colored background) with each product container during the visual inspection process
colored background) with each product container during the visual inspection process
5. The reject
vials are then mixed in with the rest of the test set and the trainee inspects
each vial while being observed 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 known rejects and ≤ 30% of blanks (false reject) is required to pass. The trainee repeats the inspection process until successfully passing three (3) times
actual defects/blanks. ≥ 70% detection of known 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-qualified 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 corrected.
If eyesight is corrected with eye glasses or contact lenses, then those must be
worn during the product inspection process.
15 comments:
If there operator, done the test 3 time
And results, 1st run 75, second run 70
Third run, 65%
What is the final result, is this operator qualified for visual inspection test
2nd q, the 3 times in 3 different days
N there same day, to include factorr fatigue
No ,each run required within critaria
What is the responsibility of the company to provide vials that are clear and in decent condition for the inspector to see flaws and rejects?
So how many vials should be tested? Wanna know the total quantity of samples should be tested.
So how many vials should be tested? Wanna know the total quantity of samples should be tested.
Can we apply this procedure for solid dosage form or is there any other inspector qualifications procedure
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