Study programme 2020-2021 | Français | ||
Méthodes analytiques: préparation des échantillons et validation | |||
Learning Activity |
Code | Lecturer(s) | Associate Lecturer(s) | Subsitute Lecturer(s) et other(s) | Establishment |
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M-ANPH-001 |
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Language of instruction | Language of assessment | HT(*) | HTPE(*) | HTPS(*) | HR(*) | HD(*) | Term |
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Français | Français | 20 | 0 | 0 | 0 | 0 | Q2 |
Organisational online arrangements for the end of Q3 2020-2021 assessments (Covid-19) |
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Organisational arrangements for the end of Q2 2020-2021 assessments (Covid-19) online or face-to-face (according to assessment schedule)
Content of Learning Activity
Analysis process will be studied in its globalitiy from experimental design to method development (sample preparation/separation/detection) and validation. Thematics of good laboratory practices (GLP), quality control in pharmacies or in industry, drugs stability and drug counterfeit drug analysis will be also reviewed.
Required Learning Resources/Tools
Power point slides available on Moodle
Recommended Learning Resources/Tools
Not applicable
Other Recommended Reading
Not applicable
Mode of delivery
Type of Teaching Activity/Activities
Evaluations
The assessment methods of the Learning Activity (AA) are specified in the course description of the corresponding Educational Component (UE)