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 |