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                             54 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A Database Quality Review Process with Interim Checks Brunelle, Rocco
2002
36 2 p. 357-367
artikel
2 A Database Quality Review Process with Interim Checks Brunelle, Rocco

36 2 p. 357-367
artikel
3 Adverse Event Reporting and Standardized Medical Terminologies: Strengths and Limitations Goldman, Stephen A.
2002
36 2 p. 439-444
artikel
4 Adverse Event Reporting and Standardized Medical Terminologies: Strengths and Limitations Goldman, Stephen A.

36 2 p. 439-444
artikel
5 Aggregate Analysis of the Export Petition and Waiver Process: A Pharmaceutical Industry Perspective Fisher, Travis S.
2002
36 2 p. 343-348
artikel
6 Aggregate Analysis of the Export Petition and Waiver Process: A Pharmaceutical Industry Perspective Fisher, Travis S.

36 2 p. 343-348
artikel
7 Analysis of the Qt Interval in Clinical Trials Dmitrienko, Alex
2002
36 2 p. 269-279
artikel
8 Analysis of The QT Interval in Clinical Trials Dmitrienko, Alex

36 2 p. 269-279
artikel
9 A Nonparametric Method for Combining Multilaboratory Data Huang, Jie
2002
36 2 p. 395-406
artikel
10 A Nonparametric Method for Combining Multilaboratory Data Huang, Jie

36 2 p. 395-406
artikel
11 Are Commercial Disease Managers Willing and Prepared to Enter the Medicare Market?* Cohen, Joshua
2002
36 2 p. 445-452
artikel
12 Are Commercial Disease Managers Willing and Prepared to Enter the Medicare Market? Cohen, Joshua

36 2 p. 445-452
artikel
13 A Review of Current Events in Human Subjects Protection Coleman, Laura
2002
36 2 p. 261-267
artikel
14 A Review of Current Events in Human Subjects Protection Coleman, Laura

36 2 p. 261-267
artikel
15 Assessment of the Immunotoxic Potential of Human Pharmaceuticals: A Workshop Report Putman, Esther
2002
36 2 p. 417-427
artikel
16 Assessment of the Immunotoxic Potential of Human Pharmaceuticals: A Workshop Report Putman, Esther

36 2 p. 417-427
artikel
17 505(b)(2) Applications: History, Science, and Experience* Johnston, Gordon
2002
36 2 p. 319-323
artikel
18 505(b)(2) Applications: History, Science, and Experience Johnston, Gordon

36 2 p. 319-323
artikel
19 Bridging Data between Two Ethnic Populations. A New Application of Matched Case-Control Methodology Sarkar, Somnath
2002
36 2 p. 349-356
artikel
20 Bridging Data between Two Ethnic Populations. A New Application of Matched Case-Control Methodology Sarkar, Somnath

36 2 p. 349-356
artikel
21 Clinical Trials: Focus on Italy Bianchi, Walter
2002
36 2 p. 387-394
artikel
22 Clinical Trials: Focus on Italy Bianchi, Walter

36 2 p. 387-394
artikel
23 Comparison of Additional Regulatory Requirements for Conducting Clinical Trials on Genetically-Modified Microorganisms and Recombinant Dna in Europe, the United States, and Canada Lee, King C.
2002
36 2 p. 379-386
artikel
24 Comparison of Additional Regulatory Requirements for Conducting Clinical Trials on Genetically-Modified Microorganisms and Recombinant DNA in Europe, the United States, and Canada Lee, King C.

36 2 p. 379-386
artikel
25 Deceptive Inquiries Made to Drug Information Departments Curran, Charles F.
2002
36 2 p. 435-438
artikel
26 Deceptive Inquiries Made to Drug Information Departments Curran, Charles F.

36 2 p. 435-438
artikel
27 Ethical Concerns in Placebo-Controlled Studies: An Analytical Approach* Cavazos, Nora
2002
36 2 p. 249-259
artikel
28 Ethical Concerns in Placebo-Controlled Studies: An Analytical Approach Cavazos, Nora

36 2 p. 249-259
artikel
29 Evaluation of Published Case Reports' Standards and Notification Ferguson, Jeffrey A.
2002
36 2 p. 303-307
artikel
30 Evaluation of Published Case Reports’ Standards and Notification Ferguson, Jeffrey A.

36 2 p. 303-307
artikel
31 From the Editor-In-Chief: “Regulatory Reform at a Crossroads” Kaitin, Kenneth I.
2002
36 2 p. 245-246
artikel
32 From the Editor-in-Chief: “Regulatory Reform at a Crossroads” Kaitin, Kenneth I.

36 2 p. 245-246
artikel
33 Guest Editor's Note: Regulatory Affairs Copmann, Thomas L.
2002
36 2 p. 247-248
artikel
34 Guest Editor’s Note: Regulatory Affairs Copmann, Thomas L.

36 2 p. 247-248
artikel
35 Japanese Perspectives on Pharmaceutical Product Release Rate Testing Kaniwa, Nahoko
2002
36 2 p. 407-415
artikel
36 Japanese Perspectives on Pharmaceutical Product Release Rate Testing Kaniwa, Nahoko

36 2 p. 407-415
artikel
37 Managing a Crisis Effectively: A Blueprint for Pharmaceutical Companies Stotka, Jennifer L.
2002
36 2 p. 325-331
artikel
38 Managing a Crisis Effectively: A Blueprint for Pharmaceutical Companies Stotka, Jennifer L.

36 2 p. 325-331
artikel
39 Prescription-to-Over-the-Counter Switch Criteria Soller, R. William
2002
36 2 p. 309-317
artikel
40 Prescription-to-over-the-Counter Switch Criteria Soller, R. William

36 2 p. 309-317
artikel
41 Pricing Policies in the Pharmaceutical Sector Capri, Stefano
2002
36 2 p. 453-464
artikel
42 Pricing Policies in the Pharmaceutical Sector Capri, Stefano

36 2 p. 453-464
artikel
43 Standard Operating Procedures for Clinical Research Coordinators Fries, Ruth Ann
2002
36 2 p. 369-377
artikel
44 Standard Operating Procedures for Clinical Research Coordinators Fries, Ruth Ann

36 2 p. 369-377
artikel
45 Taking the Package Insert into the Electronic Age* Smith, Neil V.
2002
36 2 p. 429-434
artikel
46 Taking the Package Insert into the Electronic Age Smith, Neil V.

36 2 p. 429-434
artikel
47 The Single Controlled Trial: Industry Survey Indicates That Implementation is Still a Work in Progress Milne, Christopher-Paul
2002
36 2 p. 291-302
artikel
48 The Single Controlled Trial: Industry Survey Indicates that Implementation is Still a Work in Progress Milne, Christopher-Paul

36 2 p. 291-302
artikel
49 The United States Food and Drug Administration's Risk Management Framework Steidle, Gina
2002
36 2 p. 333-341
artikel
50 The United States Food and Drug Administration’s Risk Management Framework Steidle, Gina

36 2 p. 333-341
artikel
51 Which Factors Shape and Limit the Role of the Center for Drug Evaluation and Research's Advisory Committees?* Schulman, Sara
2002
36 2 p. 281-289
artikel
52 Which Factors Shape and Limit the Role of the Center for Drug Evaluation and Research’s Advisory Committees? Schulman, Sara

36 2 p. 281-289
artikel
53 Will Data Privacy Impact Health Research? Knudsen, Lisbeth Ehlert
2002
36 2 p. 465-480
artikel
54 Will Data Privacy Impact Health Research? Knudsen, Lisbeth Ehlert

36 2 p. 465-480
artikel
                             54 gevonden resultaten
 
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