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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:
APPLICATION OF GC/MS FOR IDENTYFICATION OF THE SIDEPRODUCTS IN A PROCESS OF PREPARATION OF PRAMIPEXOLE.
Development and validation of GCMS method for the control of ethyl and izopropyl methanesulphonates in pharmaceutical substance in a form of mesilate
Development and validation of the GC method for quantitative determination of semi-volatile solvents in pharmaceutical substance Bosentan
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
Investigation of unknown impurities in cyclic dermorphin analogue by HPLC-MS
Isolation, structural elucidation and characterization of impurities in latanoprost
Method development and validation of an analytical procedure - control of residual 2-iodopropane in Latanoprost
NEW SYNTHESIS OF 11-(1-PIPERAZINYL)- DIBENZO[b,f][1,4]THIAZEPINE, A CRUCIAL INTERMEDIATE IN QUETIAPINE PRODUCTION.
The use of the hyphenated LC-MS/MS technique for the characterisation of impurity profile of Quetiapine during drug development
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