Questions and Answers
What is the main responsibility of the QC department in a pharmaceutical firm?
Sampling and testing semi-finished and finished products
Where is the setting up of specifications for raw materials typically carried out in a pharmaceutical firm?
Research and development (R&D) department
What is the primary focus of the QA department in a pharmaceutical firm?
Ensuring the application of GMPs during manufacturing
Which department is responsible for large scale manufacturing according to the formulation and procedure developed by R&D?
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Where are the analytical method development and process validation typically carried out in a pharmaceutical firm?
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Study Notes
Quality Control (QC) Department
- The main responsibility of the QC department is to ensure that the pharmaceutical products meet the required quality standards.
Setting Up Specifications
- The setting up of specifications for raw materials is typically carried out in the Quality Control (QC) department.
Quality Assurance (QA) Department
- The primary focus of the QA department is to ensure that the pharmaceutical products are manufactured according to the required quality standards and regulations.
Manufacturing Department
- The department responsible for large-scale manufacturing according to the formulation and procedure developed by Research and Development (R&D) is the Manufacturing Department.
Analytical Method Development and Process Validation
- Analytical method development and process validation are typically carried out in the Research and Development (R&D) department.
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