| 臺大學術典藏 |
2018-09-10T07:30:28Z |
Statistical validation of traditional Chinese diagnostic procedures
|
Hsiao, C.-F. and Tsou, H.-H. and Pong, A. and Liu, J.-P. and Lin, C.-H. and Chang, Y.-J. and Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T07:30:28Z |
Statistical methods for evaluating the linearity in assay validation
|
Hsieh, E.;Hsiao, C.-F.;Liu, J.-P.; Hsieh, E.; Hsiao, C.-F.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T07:29:04Z |
Statistical inference for the within-device precision of quantitative measurements in assay validation
|
CHEN-TUO LIAO; JEN-PEI LIU; Liao, C.T.; Lu, L.-T.; Liu, J.-P.; Liu, J.-P.;Lu, L.-T.;Liao, C.T. |
| 臺大學術典藏 |
2018-09-10T06:57:53Z |
Design and Analysis of Animal Studies in Pharmaceutical Development
|
Jen-Pei Liu; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:53Z |
Design and Analysis of Animal Studies in Pharmaceutical Development
|
Jen-Pei Liu; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:53Z |
Design and Analysis of Animal Studies in Pharmaceutical Development
|
Jen-Pei Liu; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:52Z |
The integrated clinical and statistical report for registration in Taiwan
|
Jen-Pei Liu; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:52Z |
The integrated clinical and statistical report for registration in Taiwan
|
Jen-Pei Liu; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:52Z |
Statistical evaluation of individual bioequivalence
|
Jen-Pei Liu; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:52Z |
Statistical evaluation of individual bioequivalence
|
Jen-Pei Liu; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:52Z |
In vitro dissolution profile comparison- Statistics and analysis of the similarity factor, f2
|
Shah, V.P.; Tsong, Y.; Sathe, P.; Liu, J.-P.; Shah, V.P.; Tsong, Y.; Sathe, P.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:52Z |
Design and Analysis of Bioavailability and Bioequivalence, third edition
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:52Z |
Design and Analysis of Bioavailability and Bioequivalence, third edition
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:52Z |
Design and Analysis of Bioavailability and Bioequivalence, third edition
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:52Z |
Design and Analysis of Clinical Trials: Concepts and Methodologies
|
Jen-Pei Liu; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:52Z |
Design and Analysis of Clinical Trials: Concepts and Methodologies
|
Jen-Pei Liu; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:52Z |
Design and Analysis of Clinical Trials: Concepts and Methodologies
|
Jen-Pei Liu; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:51Z |
On statistical evaluation of the linearity in assay validation
|
Hsieh, E.;Liu, J.-P.; Hsieh, E.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:51Z |
Commentary on "accounting for the interim safety monitoring of an adverse event upon termination of a clinical trial"
|
Liu, J.-P.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:51Z |
A two-stage design for drug screening trials based on continuous endpoints
|
Tsou, H.-H. and Hsiao, C.-F. and Chow, S.-C. and Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:50Z |
Statistical methods for targeted clinical trials under enrichment design.
|
Liu, J.P.;Lin, J.R.; Liu, J.P.; Lin, J.R.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:50Z |
Statistical issues on the diagnostic multivariate index assay for targeted clinical trials
|
Liu, J.-P.;Chow, S.-C.; Liu, J.-P.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:50Z |
Statistical evaluation of quality performance on genomic composite biomarker classifiers.
|
Liu, J.P.;Lu, L.T.; Liu, J.P.; Lu, L.T.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:56:57Z |
A non-inferiority test for diagnostic accuracy based on the paired partial areas under ROC curves
|
Li, C.-R.;Liao, C.-T.;Liu, J.-P.; Li, C.-R.; Liao, C.-T.; Liu, J.-P.; JEN-PEI LIU; CHEN-TUO LIAO |
| 臺大學術典藏 |
2018-09-10T06:56:56Z |
On the exact interval estimation for the difference in paired areas under the ROC curves
|
Li, C.-R.;Liao, C.-T.;Liu, J.-P.; Li, C.-R.; Liao, C.-T.; Liu, J.-P.; JEN-PEI LIU; CHEN-TUO LIAO |
| 臺大學術典藏 |
2018-09-10T06:56:56Z |
A permutation two one-sided tests procedure to detect minimal fold changes of gene expression levels
|
Liu, J.-P.;Liao, C.-T.;Chiu, S.-T.;Dai, J.-Y.; Liu, J.-P.; Liao, C.-T.; Chiu, S.-T.; Dai, J.-Y.; JEN-PEI LIU; CHEN-TUO LIAO |
| 臺大學術典藏 |
2018-09-10T06:24:53Z |
Some thoughts on individual bioequivalence
|
Liu, J.;Chow, S.-C.; Liu, J.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:24:53Z |
Meta-analysis for bioequivalence review
|
Chow, S.-C.;Liu, J.; Chow, S.-C.; Liu, J.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:24:53Z |
A two one-sided tests procedure for assessment of individual bioequivalence
|
Liu, J.;Chow, S.-C.; Liu, J.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:24:52Z |
Rethinking statistical approaches to evaluating drug safety
|
Liu, J.-P.; Liu, J.-P.; JEN-PEI LIU; Liu, Jen-pei |
| 臺大學術典藏 |
2018-09-10T06:24:52Z |
Statistical evaluation of similarity factor f2 as a criterion for assessment of similarity between dissolution profiles
|
Liu, J.-P.;Ma, M.C.;Chow, S.-C.; Liu, J.-P.; Ma, M.C.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:23:57Z |
Noninferiority tests based on concordance correlation coefficient for assessment of the agreement for gene expression data from microarray experiments
|
Liao, C.-T.;Lin, C.-Y.;Liu, J.-P.; Liao, C.-T.; Lin, C.-Y.; Liu, J.-P.; JEN-PEI LIU; CHEN-TUO LIAO |
| 臺大學術典藏 |
2018-09-10T05:53:08Z |
Test of equivalence and non-inferiority for diagnostic accuracy based on the paired areas under ROC curves
|
Liu, J.-P.;Ma, M.-C.;Wu, C.-Y.;Tai, J.-Y.; Liu, J.-P.; Ma, M.-C.; Wu, C.-Y.; Tai, J.-Y.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:53:08Z |
Statistical issues on the FDA conjugated estrogen tablets bioequivalence guidance
|
Liu, J.-P. and Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
Statistical Design and Analysis in Pharmaceutical Science: Validation, Process Controls, and Stability
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
Statistical Design and Analysis in Pharmaceutical Science: Validation, Process Controls, and Stability
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
Statistical Design and Analysis in Pharmaceutical Science: Validation, Process Controls, and Stability
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
The impact of outlying subjects on decision of bioequivalence
|
Ki, F.Y.C.;Liu, J.-P.;Wang, W.;Chow, S.-C.; Ki, F.Y.C.; Liu, J.-P.; Wang, W.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
Replicated crossover designs in bioavailability and bioequivalence trials
|
Liu, J.-P.;Chow, S.-C.; Liu, J.-P.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
Current issues in bioequivalence trials
|
Chow, S.-C.;Liu, J.-P.; Chow, S.-C.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
Bias of two one-sided tests procedures in assessment of bioequivalence
|
Liu, J.-P.;Weng, C.-S.; Liu, J.-P.; Weng, C.-S.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:17Z |
Tests for equivalence based on odds ratio for matched-pair design
|
Liu, J.-P.;Fan, H.-Y.;Ma, M.-C.; Liu, J.-P.; Fan, H.-Y.; Ma, M.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:17Z |
A two-stage design for bridging studies
|
Hsiao, C.-F.;Xu, J.-Z.;Liu, J.-P.; Hsiao, C.-F.; Xu, J.-Z.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:17Z |
Use of the repeated cross-over designs in assessing bioequivalence
|
Liu, J.-P.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:03:21Z |
High incidence rate of hip fracture in Taiwan: Estimated from a nationwide health insurance database
|
Chie, W.C.;Yang, R.S.;Liu, J.P.;Tsai, K.S.; Chie, W.C.; Yang, R.S.; Liu, J.P.; Tsai, K.S.; KEH-SUNG TSAI; RONG-SEN YANG; JEN-PEI LIU; WEI-CHU CHIE |
| 臺大學術典藏 |
2018-09-10T04:49:26Z |
A Bayesian noninferiority approach to evaluation of bridging studies
|
Liu, J.-P.;Hsueh, H.;Hsiao, C.-F.; Liu, J.-P.; Hsueh, H.; Hsiao, C.-F.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:49:26Z |
Recent statistical developments in bioequivalence trials - A review of the FDA guidance
|
Chow, S.-C.;Liu, J.-P.; Chow, S.-C.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:49:26Z |
Design and Analysis of Clinical Trials, second edition
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:49:26Z |
Design and Analysis of Clinical Trials, second edition
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:49:26Z |
Design and Analysis of Clinical Trials, second edition
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
