About
💻𝗖𝗢𝗨𝗥𝗦𝗘 𝗦𝗨𝗠𝗠𝗔𝗥𝗬: ✅The "Dissolution Method Development Blueprint" course provides a comprehensive overview of the dissolution testing process, tailored for professionals in the pharmaceutical industry. This course is designed to deepen understanding and enhance skills in developing robust dissolution methods, crucial for drug formulation and quality control. ✅Key areas of study include the design of discriminatory, QC release, and biorelevant dissolution methods, the significance of sink conditions, and the influence of drug properties such as amorphism, polymorphism, solvates, hydrates, and salt formation on intrinsic dissolution rates. The course emphasizes the importance of understanding the role of pH and pKa in drug solubility and absorption, crucial for effective dissolution testing. ✅Participants will engage with practical aspects of dissolution method development, including apparatus selection, medium choice, and timing for analysis. The application of the Biopharmaceutics Classification System (BCS), the use of surfactants, and analytical techniques like F2 calculation are discussed to enhance understanding of drug release and bioavailability. ✅Designed to enrich participants' methodological skills and knowledge, this course equips them to develop, optimize, and implement dissolution testing methods that align with regulatory standards and ensure the quality and efficacy of pharmaceutical products. 𝗖𝗘𝗥𝗧𝗜𝗙𝗜𝗖𝗔𝗧𝗘: 🎓Receive a certificate upon successfully finishing this course 𝗖𝗢𝗨𝗥𝗦𝗘 𝗗𝗨𝗥𝗔𝗧𝗜𝗢𝗡: ⏳316 Minutes (5.26 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