Cleaning Validation Training
PharmOut offer Cleaning Validation Training Courses throughout Asia.
The training focuses on the following high level areas of cleaning validation.
Pharmaceutical Cleaning Validation is a critical component of a Process Validation Checklist. Cleaning validation is needed to ensure HSE, WHO, ISO or FDA compliance. For both Active Pharmaceutical Ingredient (API) and Final Dosage manufacturing plants, it is recommended that you have these included in your site Validation Master Plan (VMP) as well as a written Cleaning Validation Policy.
Companies have been found to be non-compliant with FDA regulations through sole visual inspections. Our expert advice is not to just focus on the "scientific evidence" i.e. TOC or HPLC analysis and results, but to use basic visual checks as well.
If the manufacturing facility is large and intricate, it is advisable to have a separate Cleaning Validation Plan.
To be compliant we can help you write or train your employees on how to undertake these validations so that your company is compliant.
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Pharmaceutical Cleaning Validation Policy
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Cleaning Validation Master Plan
- Cleaning Validation of CIP systems
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