Advanced Pharmaceutical Technology Course
4.3/5
This course equips learners with advanced skills in pharmaceutical technology for developing modified-release antihypertensive tablets. Participants will master target product profile design, formulation strategies using Q1/Q2 sameness, excipient and polymer selection, manufacturing scale-up processes, critical parameters identification, dissolution profiling, stability studies, risk assessment, and regulatory compliance to produce high-quality, patient-centric oral therapies that enhance adherence and efficacy in contemporary pharmacy practice.
4.3 in rating
flexible workload of 4 to 360h
valid certificate in your country
What will I learn?
Gain practical expertise in designing and optimising once-daily modified-release antihypertensive tablets through in-depth study of pharmacology, biopharmaceutics, Q1/Q2 formulation approaches, excipient and polymer selection, various modified-release technologies, and target product profile development. Acquire hands-on knowledge of manufacturing pathways, critical process parameters, critical material attributes, dissolution testing, stability evaluation, risk management, and regulatory requirements essential for creating reliable, superior-quality pharmaceutical products.
Elevify advantages
Develop skills
- Design modified-release antihypertensive tablets focusing on dose, pharmacokinetics, pharmacodynamics, and patient adherence.
- Develop Q1/Q2 equivalent formulations by selecting excipients, polymers, and stability strategies.
- Select appropriate modified-release technologies like matrix, multiparticulate, or osmotic systems based on BCS classification.
- Establish robust manufacturing processes for scale-up, identifying critical process parameters, critical material attributes, and in-process controls.
- Design analytical testing plans for dissolution, HPLC assays, risk assessment, and bioequivalence alignment.
Suggested summary
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