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| Pharmaceutical Mfg. Regulations (U.S.)
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Description:
Our Pharmaceutical Mfg. Regulations (U.S.) test measures your knowledge of the regulations that govern pharmaceutical manufacturing in the United States. Designed for professionals with pharmaceutical manufacturing experience, this test covers the following topics: U.S. FDA Regulations, Buildings and Facilities, Process Control, Packaging and Labeling, Raw Materials, Equipment, Organization, and Records. This test will verify an individual's knowledge of the concepts and subjects tested. The results of this test do not imply that the individual possess the necessary skills to perform a specific procedure, nor treatment, nor is licensed, nor authorized, to practice any health care profession under any applicable laws.
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- Buildings and Facilities
- Air Handling Systems
- Building Services
- Design
- Documentation
- Batch Records, Deviations
- SOPs
- Equipment
- Design and Construction
- Maintenance, Cleaning, Automated
- Laboratory
- Stability Testing
- Testing and Release
- Organization
- Qualifications
- Responsibilities
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- Packaging and Labeling
- Examination and Issuance
- Operations
- Process Control
- Contamination
- Sampling
- Raw Materials
- Requirements
- Testing and Approval
- Records
- General Requirements
- Processing Records
- US FDA Regulations
- Applications of Regulations
- cGMP Regulations
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