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Faculty : Science and Technology
Department: process engineering
Target public: 1st Master
Fields of Specialization: pharmaceutical engineering
Course title: Drug Analysis and control
Credit: 4
Coefficient: 2
Duration: 15 weeks
Weekly timetable: 1h 30 min of course and 1h 30 min of tutorial
Place of teaching: classroom 22 (block 1)
Prof: S. Ikhlef
Contact: s.ikhlef@centre-univ-mila.dz
Availability: every Munday from 9.30am-11am in office 19 (block 4).
Evaluation methods: A final exam 60%, interogation 40%,
Responses by e-mail: I promise to reply by e-mail within 24 hours of receiving the message, except in the case of unexpected circumstances.Target Skills

By the end of this course, students will be able to:
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Understand regulatory frameworks and pharmacopoeial standards related to drug quality and control.
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Design and implement appropriate analytical strategies for identification, assay, and impurity testing.
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Apply major analytical techniques (chromatographic, spectroscopic, and titrimetric methods).
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Perform quality control tests for raw materials, finished products, sterile, biotechnological, and chiral medicines.
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Evaluate drug stability and degradation mechanisms.
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Apply pharmaceutical quality system principles, including GMP, risk management, Quality by Design, and method validation.
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Interpret analytical results and prepare technical documentation for regulatory compliance and marketing authorization.
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Prerequisites

Prerequisites
Students should have prior knowledge of:
General Chemistry (acid-base, redox, kinetics).
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Organic Chemistry (functional groups, stereochemistry, degradation reactions).
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Analytical Chemistry (titration, spectroscopy, chromatography basics).
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Physical Chemistry (pH, solubility, thermodynamics basics).
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Pharmaceutical Technology basics (dosage forms).
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Basic understanding of statistics (mean, standard deviation, calibration curve).
- Basic understanding of statistics (mean, standard deviation, calibration curve).

