BIOPHARMACEUTICAL QUALITYbiomanufacturing.org/uploads/files/13056806746070076...21CFR 211.22 for the...
Transcript of BIOPHARMACEUTICAL QUALITYbiomanufacturing.org/uploads/files/13056806746070076...21CFR 211.22 for the...
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BIOPHARMACEUTICAL QUALITY 18 July 2013Cynthia H Sarnoski PhD
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What is Quality?
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Quality
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Quality is never an accident; it is always the result of high intention,
sincere effort, intelligent direction and skillful execution;it represents the wise choice of many alternatives.
~ William A. Foster ~
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Basis for Quality Requirements
• Customer expectations• Good Business Practice• Good Science Practice• Regulatory conformance
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Regulatory Agencies
• FDA (US Food and Drug Administration)• To promote/protect public health by helping
safe/effective products reach the market in a timely way.
• EMA (European Medicines Agency)• To protect public health thru evaluation/supervision of medicines for
human.
• Other National Agencies (MHRA, IMB, ANVISA, etc.) • To ensure medicines sold/supplied to other countries
are safe, efficacious and meet required quality.
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Requirements within the Code of Federal Regulations 21CFR 211.22 for the Quality Unit
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According to US regulations,
the Quality Unit
must act independently
of production/manufacturing
in executing it’s responsibilities.
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Current Good Manufacturing Practices 21CFR 211
• Establish requirements for the manufacture of safe, effective, potent, pure and stable products.
• These include:• Facilities, Equipment, Process, and Materials are appropriate for intended purpose.
• Appropriately skilled personnel • Management Controls• Documented evidence
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Typical Quality Unit
• Quality Control+
• Quality Assurance__________________• Quality Unit
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Quality Unit Responsibilities
• Approve or reject all Production Materials• Review and approve all
• Procedures and Specifications• Validation/Qualification documents• Change Controls• Regulatory Submissions
• Ensure systems/programs are established and maintained for:• Adequate inspection, sampling, and testing• Identification of deviations, investigations and corrective
actions/preventative actions• Many, many more . . . . .
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Quality is maintained throughout the product life cycle…
Cell BanksRaw
MaterialsComponents
Cell Culture Purification ActiveSubstance
FinalProduct
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QUALITY ASSURANCE / QUALITY CONTROL
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Key Quality Processes
• Quality Control
• Product Disposition
• Marketed Product Support
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Quality Control Sampling and Testing
● Raw Materials● Media● Components● Process materials● Water● Environment● In-Process● Cell banks● Bulk drug substance● Finished Product
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Laboratory Controls
• Sample chain of custody• Compendial standards• Validated methods• Reagent control• Reference standards• Equipment Validation • Equipment Calibration• Documentation
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Testing Requirements• Adventitious agent contamination control
• Viral, microbial• Potency• Purity
• Process • Stability
• Characterization• Identity• Safety • Composition: excipients• Forensics
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Product Disposition
• Batch Record Review
• Test Record Review
• Investigations
• Change Controls
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Product Disposition continued
Key responsibilities at Product Disposition• Marketing authorization• Compliance with cGMP’s• Understanding impact of deviations --
quality, safety, efficacy, regulatory conformance• Engagement in quality systems supporting
product manufacture and control• Understanding those deviations
requiring regulatory action
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Marketed Product Support● Stability●Cell banks●Active Substance●Final Drug Product
●Annual Product Reviews
• Field Alerts & Biological Products Deviation Report (BPDRs)
• Product Quality • Inquiries• Complaints • Adverse Events
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Marketed Product Support continued
• InquiriesA non-medical comment, question or request for information such as product availability, temperature/stability, product expiry dating, dosing, product formulations/ingredients, chemical composition of componentry, etc.
• ComplaintsA report regarding an alleged defect associated with physical, chemical, microbiological, or other aspect of a product, component, or package.
• Adverse EventsAny untoward, undesired or unplanned event in the form of signs, symptoms, disease or laboratory or physiological observations occurring in a person or administered product
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FDA Web Site
www.fda.gov
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Product Quality Problems• What was the problem? How identified? • What is the root cause?• What actions were taken?• How could this have been prevented?
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Product Quality Problems
• Baxter Heparin Recall
• NECC Steroid Meningitis Contamination
• McNeil/ J&J Recall of Smelly Over-the Counter Drug
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Discussion
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