Expert Profile
Michael Levin
Owner and General Manager, Measurement Control Corporation
Michael Levin, Ph.D., has edited a very popular “Pharmaceutical Process Scale-Up” handbook (3rd edition published in 2011), and has contributed chapters on “Tablet Press Instrumentation” and “Wet Granulation: End-Point Determination and Scale-Up” in the Encyclopedia of Pharmaceutical Technology. For more than 30 years he has managed an instrumentation company providing monitoring and real-time process data on pharmaceutical solid dosage equipment.
Trainings by Expert
Process Analytical Technology (PAT): The Impact on Pharmaceuticals Manufacturing and Validation Needs/Requirements
Category:
Drugs and Chemicals (Pharma)
,
Quality and Safety
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Supply Chain and Manufacturing
,
Drug Development
,
Life sciences QA/QC
,
Research & Development
,
Drug R & D
,
Life Sciences
,
QA/QC
How to Properly Monitor Process and Performance of Pharmaceutical Solid Dosage Equipment
Category:
Drugs and Chemicals (Pharma)
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All FDA Regulated Industry
,
Quality Management
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GXP Pharmaceutical
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Drug and Device Approvals
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Quality and Safety
,
Drug Development
,
Best practices
,
Drugs Regulations
,
Risk Management & Controls
,
All FDA Regulated Functions
,
Audit & Inspection-Role
,
Quality Audit
,
All FDA Reg. based Audit
,
Drugs Inspections
,
Manufacturing Quality
,
Life sciences QA/QC
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Research & Development
,
Drug R & D
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Common FDA Regulations
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QA/QC
How to Implement the FDA SUPAC Guidance
Category:
Drugs and Chemicals (Pharma)
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Biotechnology
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Testing and Validation
,
Quality and Safety
,
Supply Chain and Manufacturing
,
Drug Development
,
Quality & Safety
,
Technologies and Processes
,
Life sciences QA/QC
,
Regulations & Guidances
,
Life Sciences
,
QA/QC
Qualification of Process Analytical Technology (PAT) Based Control Strategies for Batch & Continuous Manufacturing
Category:
Drugs and Chemicals (Pharma)
