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Dissolution testing as a prognostic tool for oral drug absorption : Immediate release dosage forms

Pharmaceutical research, 1998, Vol.15 (1), p.11-22

1998

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Bioanalytical method validation--a revisit with a decade of progress

Pharmaceutical research, 2000-12, Vol.17 (12), p.1551-1557

2000

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Analytic Solution for the RL Electric Circuit Model in Fractional Order

Abstract and Applied Analysis, 2014-01, Vol.2014 (2014), p.497-501-460

2014

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Review of global regulations concerning biowaivers for immediate release solid oral dosage forms

European journal of pharmaceutical sciences, 2006-11, Vol.29 (3-4), p.315-324

2006

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Biopharmaceutics classification system: The scientific basis for biowaiver extensions

Pharmaceutical research, 2002-07, Vol.19 (7), p.921-925

2002

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An epidemic outbreak of Vibrio Cholerae El Tor 01 serotype ogawa biotype in a Lalpur town, Jamnagar, India

Journal of postgraduate medicine, 2012-01, Vol.58 (1), p.14-18

2012

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Evaluation of the reach and impact of a UK campaign highlighting obesity as a cause of cancer among the general public and Members of Parliament

Public health (London), 2023-06, Vol.219, p.131-138

2023

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Dermal absorption for pesticide health risk assessment: Harmonization of study design and data reporting for North American Regulatory submissions

Regulatory toxicology and pharmacology, 2017-11, Vol.90, p.197-205

2017

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Bioequivalence of topical dermatological dosage forms : Methods of evaluation of bioequivalence

Pharmaceutical research, 1998-02, Vol.15 (2), p.167-171

1998

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Developing and advancing dry powder inhalation towards enhanced therapeutics

European journal of pharmaceutical sciences, 2013-01, Vol.48 (1-2), p.181-194

2013

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Dissolution testing as a prognostic tool for oral drug absorption : Dissolution behavior of glibenclamide

Pharmaceutical research, 2000-04, Vol.17 (4), p.439-444

2000

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In vitro dissolution profile comparison-statistics and analysis of the similarity factor, f2

Pharmaceutical research, 1998-06, Vol.15 (6), p.889-896

1998

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In-vitro dissolution profile comparison : Statistics and analysis, model dependent approach

Pharmaceutical research, 1996-12, Vol.13 (12), p.1799-1803

1996

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A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability

Pharmaceutical research, 1995-03, Vol.12 (3), p.413-420

1995

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Validation of bioanalytical methods

Pharmaceutical research, 1991-04, Vol.8 (4), p.421-426

1991

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Assessment of value and applications of in vitro testing of topical dermatological drug products

Pharmaceutical research, 1999-09, Vol.16 (9), p.1325-1330

1999

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An Efficient Pan-Sharpening Method via a Combined Adaptive PCA Approach and Contourlets

IEEE transactions on geoscience and remote sensing, 2008-05, Vol.46 (5), p.1323-1335

2008

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A framework for semantic reconciliation of disparate earth observation thematic data

Computers & geosciences, 2009-04, Vol.35 (4), p.761-773

2009

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The effect of gelatin cross-linking on the bioequivalence of hard and soft gelatin acetaminophen capsules

Pharmaceutical research, 2000-08, Vol.17 (8), p.962-966

2000

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The relative bioavailability and in vivo-in vitro correlations for four marketed carbamazepine tablets

Pharmaceutical research, 1998-11, Vol.15 (11), p.1787-1791

1998

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The bioinequivalence of carbamazepine tablets with a history of clinical failures

Pharmaceutical research, 1992-12, Vol.9 (12), p.1612-1616

1992

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Evaluation of orally administered highly variable drugs and drug formulations

Pharmaceutical research, 1996-11, Vol.13 (11), p.1590-1594

1996

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Development of in vivo bioequivalence methodology for dermatologic corticosteroids based on pharmacodynamic modeling

Clinical pharmacology and therapeutics, 1999-10, Vol.66 (4), p.346-357

1999

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Variability in the bioavailability of phenytoin capsules in males and females

Pharmaceutical research, 2001-03, Vol.18 (3), p.394-397

2001

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In vitro dissolution of sparingly water-soluble drug dosage forms

International journal of pharmaceutics, 1995-10, Vol.125 (1), p.99-106

1995

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Dissolution testing as a prognostic tool for oral drug absorption : Immediate release dosage forms

Bioanalytical method validation--a revisit with a decade of progress

Analytic Solution for the RL Electric Circuit Model in Fractional Order

Review of global regulations concerning biowaivers for immediate release solid oral dosage forms

Biopharmaceutics classification system: The scientific basis for biowaiver extensions

An epidemic outbreak of Vibrio Cholerae El Tor 01 serotype ogawa biotype in a Lalpur town, Jamnagar, India

Evaluation of the reach and impact of a UK campaign highlighting obesity as a cause of cancer among the general public and Members of Parliament

Dermal absorption for pesticide health risk assessment: Harmonization of study design and data reporting for North American Regulatory submissions

Bioequivalence of topical dermatological dosage forms : Methods of evaluation of bioequivalence

Developing and advancing dry powder inhalation towards enhanced therapeutics

Dissolution testing as a prognostic tool for oral drug absorption : Dissolution behavior of glibenclamide

In vitro dissolution profile comparison-statistics and analysis of the similarity factor, f2

In-vitro dissolution profile comparison : Statistics and analysis, model dependent approach

A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability

Validation of bioanalytical methods

Assessment of value and applications of in vitro testing of topical dermatological drug products

An Efficient Pan-Sharpening Method via a Combined Adaptive PCA Approach and Contourlets

A framework for semantic reconciliation of disparate earth observation thematic data

The effect of gelatin cross-linking on the bioequivalence of hard and soft gelatin acetaminophen capsules

The relative bioavailability and in vivo-in vitro correlations for four marketed carbamazepine tablets

The bioinequivalence of carbamazepine tablets with a history of clinical failures

Evaluation of orally administered highly variable drugs and drug formulations

Development of in vivo bioequivalence methodology for dermatologic corticosteroids based on pharmacodynamic modeling

Variability in the bioavailability of phenytoin capsules in males and females

In vitro dissolution of sparingly water-soluble drug dosage forms

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