1. Acquired knowledge implementation in a routine control of pharmaceutical ingredients and pharmaceutical dosage forms 2. To explain and apply Pharmacopoeial requirements in pharmaceutical ingredients and pharmaceutical dosage forms testing 3. To select the appropriate analytical method for the control of medicines 4. To demonstrate and explain the importance of analytical method development and validation 5. To interpret and apply current regulatory requirements for the quality control of medicines
Name | Lectures | Exercises | Laboratory |
---|---|---|---|
TIJANA MIĆOVIĆ | 3x1 24B+11S+1P | ||
VALENTINA JAUKOVIĆ | 3x2 24B+11S+1P |