Security Test alice
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0
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239
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May 30, 2024
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Can we divided a single SOP in two parts through change control
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2
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509
|
May 27, 2024
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Qualification Supplier
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1
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423
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May 27, 2024
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Manufacturing date for reprocess batch
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|
2
|
3160
|
May 14, 2024
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Vernacular language SOPs
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0
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367
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May 4, 2024
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CCIT testing removal
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|
0
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291
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April 29, 2024
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Retention of Costly and Large Size FG retention samples of Veterinary Product
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4
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338
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April 22, 2024
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Permitted daily exposure PDE
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|
1
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595
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April 22, 2024
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Particle sample in sterile facility in API Plant
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0
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292
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April 16, 2024
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What are the guidelines for artworks in pharmaceutical package
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0
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463
|
April 12, 2024
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Process Validation
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5
|
996
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April 16, 2024
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SOP approval not done from QA
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2
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729
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March 29, 2024
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Reworking and reprocessing of coated tablets
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2
|
923
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March 25, 2024
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How to apply for DMF for Flavouring Agent
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0
|
420
|
March 14, 2024
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Change control for a complete new method
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2
|
831
|
March 13, 2024
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The packaging item used for the storage of Bulk tablets
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3
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365
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March 13, 2024
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Water Testing of Phase I, II & III
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2
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733
|
February 26, 2024
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Can we keep two coating pan in one room
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3
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591
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February 23, 2024
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Excess powder in blister and tablet surface
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2
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571
|
February 20, 2024
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Validation master plan and change control for the same
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|
1
|
729
|
February 15, 2024
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Annual product quality review (APQR)
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|
13
|
7551
|
February 15, 2024
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Exploring the Crucial Role of Balance Qualification in the Pharmaceutical Industry
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2
|
650
|
February 1, 2024
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Procedure of OOS
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5
|
1257
|
January 19, 2024
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Product Quality Review
|
|
0
|
508
|
January 17, 2024
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Can I prepare one common process Validation Protocol for 2 different batch size of same product & area
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2
|
775
|
January 6, 2024
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SOP for Ointment mixer
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0
|
370
|
January 5, 2024
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Specific guidelines for employing logbooks in the pharmaceutical industry
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|
7
|
2042
|
December 24, 2023
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What is Room temperature definition?
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0
|
822
|
December 13, 2023
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Leak test apparatus
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|
0
|
757
|
December 12, 2023
|
Validation master plan (late)
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|
2
|
551
|
December 7, 2023
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