Premises (Equipments)
Procedures
| Document Description | Price (USD) | Click To Purchase |
|---|---|---|
|
Document Title: Equipment Cleaning and Sanitizing Procedure Document Purpose: The purpose of this document is to establish the system (procedure) to clean and sanitize the corporate production equipment.
|
31.50 $ |
|
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Document Title: Equipment Cleaning Validation Policy Document Purpose: The purpose of this document is to describe the corporate cleaning validation requirements for equipments used in the manufacture of pharmaceutical products, and biological drugs.
|
147.00 $ |
|
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Document Title: Equipment Cleaning: Acceptance Criteria Calculation Document Purpose: The purpose of this procedure is to provide corporate QA Person with the equation to calculate the Residual Cleaning Limit (RCL), based upon the next product to follow, for products manufactured in dedicated equipment.
|
31.50 $ |
|
|
Document Title: Equipment Design Requirements Document Purpose: This SOP is to define the company equipment's design policy to ensure product safety.
|
21.00 $ |
|
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Document Title: Equipment Qualification Document Purpose: The purpose of this policy is to describe the equipment qualification requirements, as specified in the International Conference on Harmonization (ICH) Guideline; “Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients.
|
157.50 $ |
|
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Document Title: Equipment Validation Guideline Document Purpose: The purpose of this document is to provide corporate manufacturing sites with the necessary information on equipments validation requirements for sterile and non-sterile dosage forms.
|
115.50 $ |
|
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Document Title: Thermometer Using and Calibrating Document Purpose: To ensure that thermometers used are correctly and frequently calibrated for accuracy.
|
21.00 $ |
