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dr Elżbieta U. Stolarczyk

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Affiliation:


Instytut Farmaceutyczny

address: Rydygiera 8, Warszawa, 01-793, Poland
phone: +48-22-4563900
fax: +48-22-4563838
web: http://www.ifarm.waw.pl

Participant:


V Multidyscyplinarna Konferencja Nauki o Leku

began: 2006-05-15
ended: 2006-05-17
Presented:

V Multidyscyplinarna Konferencja Nauki o Leku

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

Participant:


VI Multidyscyplinarna Konferencja Nauki o Leku

began: 2008-05-25
ended: 2008-05-29
Presented:

VI Multidyscyplinarna Konferencja Nauki o Leku

Isolation, structural elucidation and characterization of impurities in latanoprost

Participant:


VII Multidyscyplinarna Konferencja Nauki o Leku

began: 2010-05-09
ended: 2010-05-13
Presented:

VII Multidyscyplinarna Konferencja Nauki o Leku

The use of the hyphenated LC-MS/MS technique for the characterisation of impurity profile of Quetiapine during drug development

Participant:


VIII Multidyscyplinarna Konferencja Nauki o Leku

began: 2012-05-29
ended: 2012-06-02
Presented:

VIII Multidyscyplinarna Konferencja Nauki o Leku

Development and validation of GCMS method for the control of ethyl and izopropyl methanesulphonates in pharmaceutical substance in a form of mesilate

Participant:


IX Multidyscyplinarna Konferencja Nauki o Leku

began: 2014-05-11
ended: 2014-05-15
Presented:

IX Multidyscyplinarna Konferencja Nauki o Leku

Development and validation of the GC method for quantitative determination of semi-volatile solvents in pharmaceutical substance Bosentan

Publications:


  1. APPLICATION OF GC/MS FOR IDENTYFICATION OF THE SIDEPRODUCTS IN A PROCESS OF PREPARATION OF PRAMIPEXOLE.
  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. 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
  5. Investigation of unknown impurities in cyclic dermorphin analogue by HPLC-MS
  6. Isolation, structural elucidation and characterization of impurities in latanoprost
  7. Method development and validation of an analytical procedure - control of residual 2-iodopropane in Latanoprost
  8. NEW SYNTHESIS OF 11-(1-PIPERAZINYL)- DIBENZO[b,f][1,4]THIAZEPINE, A CRUCIAL INTERMEDIATE IN QUETIAPINE PRODUCTION.
  9. The use of the hyphenated LC-MS/MS technique for the characterisation of impurity profile of Quetiapine during drug development



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