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- Piotr J. Rudzki
e-mail:
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phone:
+48-22-4563848
fax:
+48-22-4563838
web:
http://www.ifarm.eu
interest(s):
bioavailability, bioequivalence, bioanalytical method validation, mass spectrometry
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
LC-MS DETERMINATION OF TAMSULOSIN IN HUMAN PLASMA
Participant:
VI Multidyscyplinarna Konferencja Nauki o Leku
began:
2008-05-25
ended:
2008-05-29
Presented:
VI Multidyscyplinarna Konferencja Nauki o Leku
Application of confidence intervals to bioanalytical method validation
Participant:
VIII Multidyscyplinarna Konferencja Nauki o Leku
began:
2012-05-29
ended:
2012-06-02
Presented:
VIII Multidyscyplinarna Konferencja Nauki o Leku
Validation of bioanalytical methods according to new European Medicines Agency guideline
Publications:
Application of confidence intervals to bioanalytical method validation
Bioequivalence study of 500 mg cefuroxime film-coated tablets in healthy volunteers
Bioequivalence study of ondansetron film-coated tablets in healthy volunteers
Comparison of bisoprolol pharmacokinetics after 10 mg oral administration of Bisocard and reference formulation to healthy subjects
Determination of Sunitinib in human plasma using LC/MS
Development and validation of a liquid chromatography / single quadrupole mass spectrometry method for the determination of aripiprazole in human plasma
Development and validation of LC-MS method for determination of lapatinib in human plasma
LC-MS DETERMINATION OF TAMSULOSIN IN HUMAN PLASMA
Optimization of cloud-point extraction method for determination of bisoprolol in human plasma by LC-MS/MS
Validated HPLC method for the determination of temozolomide in human plasma
Validated HPLC-UV method for determination of capecitabine in human plasma
Validated LC-MS/MS method for the complementary determination of free and total genistein in human plasma
Validation of bioanalytical methods according to new European Medicines Agency guideline
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