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  • 20Steps
Get a certificate by completing the program.


๐Ÿ’ป๐—–๐—ข๐—จ๐—ฅ๐—ฆ๐—˜ ๐—ฆ๐—จ๐— ๐— ๐—”๐—ฅ๐—ฌ: โœ…Method Validation Mastery course caters to professionals in the pharmaceutical field, focusing on Quality Assurance, Quality Control, Manufacturing, Analytical Research, and Regulatory Affairs. โœ…It offers an in-depth look at critical aspects of analytical methods and validation processes, aiming to enhance expertise in protocol review, understand key differences such as accuracy vs. trueness and specificity vs. selectivity, and tackle challenges in method validation. โœ…Participants will learn about the significance of the residual sum of squares, the nuances of dose proportionate vs. pseudo dose proportionate formulations, and delve into the workings of UV & PDA detectors. โœ…The course also covers peak purity assessment, the importance of forced degradation studies, and various validation techniques including validation, revalidation, and cross-validation. โœ…Special emphasis is placed on regulatory compliance, comparing ICH guidelines with ANVISA's regulations on linearity, forced degradation, and metal ion oxidation. โœ…Designed for those seeking to deepen their analytical and regulatory knowledge, this course is a comprehensive resource for advancing in the pharmaceutical industry. ๐—–๐—˜๐—ฅ๐—ง๐—œ๐—™๐—œ๐—–๐—”๐—ง๐—˜: ๐ŸŽ“Receive a certificate upon successfully finishing this course ๐—–๐—ข๐—จ๐—ฅ๐—ฆ๐—˜ ๐——๐—จ๐—ฅ๐—”๐—ง๐—œ๐—ข๐—ก: โณ285 Minutes (4.75 Hours) ๐—Ÿ๐—”๐—ก๐—š๐—จ๐—”๐—š๐—˜: ๐Ÿ“–English ๐—ฆ๐—˜๐—Ÿ๐—™ ๐—ฃ๐—”๐—–๐—˜๐—— ๐—Ÿ๐—˜๐—”๐—ฅ๐—ก๐—œ๐—ก๐—š: ๐ŸŒOffered as an online course featuring pre-recorded videos and structured for distance learning, this program is available to participants globally. ๐—Ÿ๐—œ๐—™๐—˜๐—ง๐—œ๐— ๐—˜ ๐—”๐—–๐—–๐—˜๐—ฆ๐—ฆ: ๐ŸŽงYou will have lifetime access to the course

You can also join this program via the mobile app.



Single Payment
2 Plans Available
From โ‚น8,990.00


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