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- Piotr J. Rudzki

e-mail:
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:


  1. Application of confidence intervals to bioanalytical method validation
  2. Bioequivalence study of 500 mg cefuroxime film-coated tablets in healthy volunteers
  3. Bioequivalence study of ondansetron film-coated tablets in healthy volunteers
  4. Comparison of bisoprolol pharmacokinetics after 10 mg oral administration of Bisocard and reference formulation to healthy subjects
  5. Determination of Sunitinib in human plasma using LC/MS
  6. Development and validation of a liquid chromatography / single quadrupole mass spectrometry method for the determination of aripiprazole in human plasma
  7. Development and validation of LC-MS method for determination of lapatinib in human plasma
  8. LC-MS DETERMINATION OF TAMSULOSIN IN HUMAN PLASMA
  9. Optimization of cloud-point extraction method for determination of bisoprolol in human plasma by LC-MS/MS 
  10. Validated HPLC method for the determination of temozolomide in human plasma
  11. Validated HPLC-UV method for determination of capecitabine in human plasma
  12. Validated LC-MS/MS method for the complementary determination of free and total genistein in human plasma
  13. Validation of bioanalytical methods according to new European Medicines Agency guideline



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