Laboratory Qualification & Validation ( 5 Sessions)
Write your review
One of the most critical factors in developing and marketing pharmaceutical drug substances and drug products today is ensuring that the analytical methods used for analysis can generate valid data upon which business and regulatory decisions can be made. FDA, ICH and USP have each recognized the importance of this to the drug development process and have separately expanded method validation requirements in recent years.
Who should attend ?
You must have 1 year of on-the-job experience in Quality Control or Quality Assurance.
- Analytical Instrument qualification
- Analytical Method validation ( Assay, Dissolution, Impurities& Identification)
- Minimum Experience
- 1 Year
- Number of Sessions
- Session Time (/h)
- Price in Egyptian Pounds
- Starting Date
You might also like
chat Comments (0)
No customer reviews for the moment.