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Tag: traceability

Verify Integrity of Tamper-Evident Seals During Packaging

Posted on May 16, 2025 By digi

Verify Integrity of Tamper-Evident Seals During Packaging Check Tamper-Evident Seals for Integrity During Packaging Remember: Tamper-evident seals must be visually verified during packaging to ensure they are applied correctly and uncompromised. Why This Matters in GMP Tamper-evident packaging is a vital mechanism for protecting pharmaceutical products against manipulation and counterfeiting. These seals serve as visible…

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GMP Tips

Review Equipment Logbooks for Completeness During GMP Audits

Posted on May 15, 2025 By digi

Review Equipment Logbooks for Completeness During GMP Audits Ensure Equipment Logbooks Are Complete Before Every Audit Remember: Incomplete or inconsistent logbooks can jeopardize audit outcomes—always verify records are complete and current. Why This Matters in GMP Equipment logbooks document the history of usage, cleaning, calibration, and maintenance for every critical asset in a GMP facility….

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GMP Tips

Maintain Access Logs for Electronic GMP Systems to Ensure Accountability

Posted on May 10, 2025 By digi

Maintain Access Logs for Electronic GMP Systems to Ensure Accountability Keep Detailed Access Logs for Electronic GMP Systems Remember: Every login, action, or change in GMP electronic systems must be logged and traceable to ensure accountability. Why This Matters in GMP Electronic systems are integral to data collection, analysis, and product release decisions in pharmaceutical…

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GMP Tips

Do Not Include Unrelated Documents in GMP Production Records

Posted on May 7, 2025 By digi

Do Not Include Unrelated Documents in GMP Production Records Keep Production Records Free of Unrelated Documents Remember: Only include relevant, approved documents in GMP production records to preserve clarity and compliance. Why This Matters in GMP GMP documentation must be organized, traceable, and limited to approved content. Inserting unrelated notes, calculations, or non-referenced documents into…

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GMP Tips

Label In-Process Samples with Date and Initials for Traceability

Posted on May 5, 2025 By digi

Label In-Process Samples with Date and Initials for Traceability Always Label In-Process Samples with Date and Initials Remember: In-process samples must be clearly labeled with the sampling date and initials of the person who collected them. Why This Matters in GMP In-process samples provide real-time insight into product quality at different stages of manufacturing. Without…

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GMP Tips

Use Material Transfer Notes (MTNs) When Moving Raw Materials

Posted on May 3, 2025 By digi

Use Material Transfer Notes (MTNs) When Moving Raw Materials Do Not Move Materials Without a Valid Material Transfer Note Remember: Always accompany material movement with an authorized MTN to preserve traceability and control. Why This Matters in GMP Material Transfer Notes (MTNs) serve as vital documents that authorize and document the movement of raw and…

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GMP Tips

Verify Batch Yield Calculations Before Finalizing Manufacturing Records

Posted on May 3, 2025 By digi

Verify Batch Yield Calculations Before Finalizing Manufacturing Records Always Verify Batch Yield Calculations Before BMR Finalization Remember: Confirm all yield values before signing off on the Batch Manufacturing Record (BMR). Why This Matters in GMP Yield reconciliation is a critical component of GMP manufacturing that ensures raw materials are efficiently converted into finished products. Yield…

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GMP Tips

Avoid Operating Equipment Without Completing Logbook Entries

Posted on May 2, 2025 By digi

Avoid Operating Equipment Without Completing Logbook Entries Never Use Equipment Without Properly Completing Its Logbook Remember: Equipment must not be operated unless logbook entries for prior and current usage are accurately recorded. Why This Matters in GMP In GMP-compliant environments, every piece of equipment has its own identity and operational history. Equipment logbooks serve as…

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GMP Tips

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  • Do Not Stockpile Rejected Units in Pharmaceutical Dispensing Areas

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traceability

  • Verify Integrity of Tamper-Evident Seals During Packaging
  • Review Equipment Logbooks for Completeness During GMP Audits
  • Maintain Access Logs for Electronic GMP Systems to Ensure Accountability
  • Do Not Include Unrelated Documents in GMP Production Records
  • Label In-Process Samples with Date and Initials for Traceability
  • Use Material Transfer Notes (MTNs) When Moving Raw Materials
  • Verify Batch Yield Calculations Before Finalizing Manufacturing Records
  • Avoid Operating Equipment Without Completing Logbook Entries

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