About
💻𝗖𝗢𝗨𝗥𝗦𝗘 𝗦𝗨𝗠𝗠𝗔𝗥𝗬: ✅Method Validation Mastery course caters to professionals in the pharmaceutical field, focusing on Quality Assurance, Quality Control, Manufacturing, Analytical Research, and Regulatory Affairs. ✅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. ✅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. ✅The course also covers peak purity assessment, the importance of forced degradation studies, and various validation techniques including validation, revalidation, and cross-validation. ✅Special emphasis is placed on regulatory compliance, comparing ICH guidelines with ANVISA's regulations on linearity, forced degradation, and metal ion oxidation. ✅Designed for those seeking to deepen their analytical and regulatory knowledge, this course is a comprehensive resource for advancing in the pharmaceutical industry. 𝗖𝗘𝗥𝗧𝗜𝗙𝗜𝗖𝗔𝗧𝗘: 🎓Receive a certificate upon successfully finishing this course 𝗖𝗢𝗨𝗥𝗦𝗘 𝗗𝗨𝗥𝗔𝗧𝗜𝗢𝗡: ⏳285 Minutes (4.75 Hours) 𝗟𝗔𝗡𝗚𝗨𝗔𝗚𝗘: 📖English 𝗦𝗘𝗟𝗙 𝗣𝗔𝗖𝗘𝗗 𝗟𝗘𝗔𝗥𝗡𝗜𝗡𝗚: 🌏Offered as an online course featuring pre-recorded videos and structured for distance learning, this program is available to participants globally. 𝗟𝗜𝗙𝗘𝗧𝗜𝗠𝗘 𝗔𝗖𝗖𝗘𝗦𝗦: 🎧You will have lifetime access to the course
You can also join this program via the mobile app. Go to the app