GMP compliance – Pharma GMP

Review Environmental Monitoring Data Trends to Ensure GMP Compliance

digi — Fri, 13 Jun 2025 22:01:45 +0000

Review Environmental Monitoring Data Trends to Ensure GMP Compliance Trend Environmental Monitoring Data to Strengthen GMP Controls Remember: GMP requires not just environmental monitoring—but regular trend analysis of results to detect early warning signs and prevent excursions. Why This Matters in GMP Environmental Monitoring (EM) is a core GMP requirement for cleanrooms and sterile zones....

Avoid Water Stagnation in GMP Drains and Sinks to Prevent Contamination

digi — Fri, 13 Jun 2025 08:23:45 +0000

Avoid Water Stagnation in GMP Drains and Sinks to Prevent Contamination Prevent Water Stagnation in Drains and Sinks to Avoid Microbial Risk Remember: Water stagnation in GMP areas is a major source of microbial growth—ensure drains and sinks are regularly inspected, cleaned, and dried. Why This Matters in GMP Standing water is a fertile breeding...

Test Compressed Air for Microbial Contamination in GMP Utilities

digi — Thu, 12 Jun 2025 21:27:36 +0000

Test Compressed Air for Microbial Contamination in GMP Utilities Verify Compressed Air for Microbial Contamination in GMP Operations Remember: Compressed air used in manufacturing must be monitored routinely for microbial and particulate contamination to ensure utility integrity. Why This Matters in GMP Compressed air is extensively used in pharmaceutical manufacturing—for equipment operation, product contact applications,...

Always Perform Swab Sampling After Cleaning Validation

digi — Thu, 12 Jun 2025 11:37:29 +0000

Always Perform Swab Sampling After Cleaning Validation Conduct Swab Sampling Post Cleaning Validation to Confirm Effectiveness Remember: Swab sampling must be performed after cleaning validation to ensure no residues or contaminants remain before equipment reuse. Why This Matters in GMP Cleaning validation establishes that manufacturing equipment can be cleaned to a predetermined level of cleanliness....

Verify Integrity of Double-Door Pass Boxes to Prevent Cross Contamination

digi — Thu, 12 Jun 2025 00:50:20 +0000

Verify Integrity of Double-Door Pass Boxes to Prevent Cross Contamination Ensure Proper Functioning of Double-Door Pass Boxes in GMP Cleanrooms Remember: GMP mandates validated, interlocked pass boxes with door integrity checks to prevent contamination during material transfer between classified areas. Why This Matters in GMP Pass boxes act as controlled transfer points between rooms of...

Never Introduce Uncontrolled Paper Materials into Sterile GMP Areas

digi — Wed, 11 Jun 2025 11:00:58 +0000

Never Introduce Uncontrolled Paper Materials into Sterile GMP Areas Do Not Introduce Uncontrolled Paper Into Sterile Areas Remember: Paper materials must be controlled, sterile-compatible, and pre-approved before entering aseptic environments to avoid particulate and microbial contamination. Why This Matters in GMP Conventional paper products are a major source of particulates and microbial load. When brought...

Use Disinfectant Rotation Schedules as Per GMP SOPs

digi — Wed, 11 Jun 2025 00:31:13 +0000

Use Disinfectant Rotation Schedules as Per GMP SOPs Rotate Disinfectants According to SOP to Prevent Microbial Resistance Remember: Disinfectants must be rotated regularly as per SOP—this is essential to prevent resistance and maintain cleanroom hygiene. Why This Matters in GMP Repeated use of a single disinfectant can lead to microbial adaptation, reducing its efficacy over...

Never Adjust Cleanroom Thermostats Without QA Notification

digi — Tue, 10 Jun 2025 11:00:09 +0000

Never Adjust Cleanroom Thermostats Without QA Notification Do Not Adjust Cleanroom Thermostats Without QA Authorization Remember: Any change to cleanroom temperature settings must be done only after QA approval—unauthorized changes can lead to GMP violations. Why This Matters in GMP Cleanroom environments rely on strict control of temperature, humidity, pressure, and airflow to maintain classification...

Wear Overshoes Before Entering Grade C Zones to Maintain GMP Hygiene

digi — Mon, 09 Jun 2025 21:02:33 +0000

Wear Overshoes Before Entering Grade C Zones to Maintain GMP Hygiene Use Overshoes When Entering Grade C Cleanroom Areas Remember: Wearing overshoes before entering Grade C zones is a mandatory step in cleanroom gowning to minimize contamination from external footwear. Why This Matters in GMP Footwear is a significant vector for introducing external contaminants—dust, microbes,...

Do Not Overfill Waste Bins in GMP Cleanrooms to Prevent Contamination

digi — Mon, 09 Jun 2025 06:47:49 +0000

Do Not Overfill Waste Bins in GMP Cleanrooms to Prevent Contamination Do Not Allow Waste Bins to Overflow in GMP Cleanrooms Remember: Waste containers in cleanrooms must be emptied regularly—overflowing bins pose microbial and particulate contamination risks. Why This Matters in GMP Waste bins in GMP environments collect used materials, garments, wipes, and discarded packaging—all...