- Aleksandra Groman

Affiliation:

Pharmaceutical Research Institute

Participant:

VI Multidyscyplinarna Konferencja Nauki o Leku

Participant:

VII Multidyscyplinarna Konferencja Nauki o Leku

Participant:

VIII Multidyscyplinarna Konferencja Nauki o Leku

Publications:

1. Determination of organic volatile impurities in Nepafenac by GC method
2. Development and validation of GCMS method for the control of ethyl and izopropyl methanesulphonates in pharmaceutical substance in a form of mesilate
3. Development and validation of the GC method for quantitative determination of semi-volatile solvents in pharmaceutical substance Bosentan
4. Development of HPLC and GC methods for analysis of Zolmitriptan of pharmaceutical purity
5. GC METHOD FOR QUANTITATIVE DETER- MINATION OF RESIDUAL 2-(2-CHLORO- ETOXY)ETHANOL (CEE) AND N-METHYL- 2-PYRROLIDINONE (NMP) IN PHARMACEU- TICAL ACTIVE SUBSTANCE
6. Method development and validation of an analytical procedure - control of residual 2-iodopropane in Latanoprost
7. Preparation and physicochemical properties of crystalline forms and amorphous pemetrexed disodium
8. Synthesis of potential impurities of loteprednol etabonate and methods for chemical purity determination
9. Validation of a HPLC method for LI-S analysis
10. Validation of an analytical procedure – control of residual 8 solvents in a pharmaceutical substance
11. VALIDATION OF AN ANALYTICAL PROCEDURE - CONTROL OF RESIDUAL 9 SOLVENTS IN PHARMACEUTICAL SUBSTANCE
12. VALIDATION OF AN ANALYTICAL PROCEDURE - CONTROL OF RESIDUAL ETHANOL, 2-PROPANOL AND ETHYL ACETATE IN PHARMACEUTICAL SUBSTANCE