nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
“Aboutness” and other Problems of Text Retrieval in the Pharmaceutical Industry
|
Abbott, Robert |
|
1997 |
31 |
1 |
p. 125-135 |
artikel |
2 |
Accounting for Noncompliance in the Design of Clinical Trials
|
Albert, Jeffrey M. |
|
1997 |
31 |
1 |
p. 157-165 |
artikel |
3 |
A Matrix Method for the Evaluation of Therapeutic Agents: A Framework Based on Disease Process-Oriented Mechanisms of Drug Action and Their Effectiveness
|
Bjornsson, Thorir D. |
|
1997 |
31 |
1 |
p. 105-110 |
artikel |
4 |
A Model for Osteoporosis Education of Students and Health Professionals
|
Papaioannou, Alexandra |
|
1997 |
31 |
1 |
p. 287-291 |
artikel |
5 |
A New and Fast Drug Approval System in Europe
|
Sauer, Fernand |
|
1997 |
31 |
1 |
p. 1-6 |
artikel |
6 |
An Index of United States Regulations Pertaining to Labeling of Prescription Drugs
|
Curran, Charles F. |
|
1997 |
31 |
1 |
p. 57-62 |
artikel |
7 |
An Innovative Concept in Pharmaceutical Drug Development
|
Tiggemann, Rolf F. |
|
1997 |
31 |
1 |
p. 119-124 |
artikel |
8 |
An Integrated Approach to the Preparation of Global CMC Dossiers
|
Karlton, Peter C. |
|
1997 |
31 |
1 |
p. 237-242 |
artikel |
9 |
Appropriate Endpoints for Renal Transplantation Clinical Trials
|
Ponticelli, Claudio |
|
1997 |
31 |
1 |
p. 207-212 |
artikel |
10 |
A Proactive Approach to Clinical Trial Material Preparation: The Manufacturing, Packaging, and Labeling Protocol
|
Ehrich, Jan A. |
|
1997 |
31 |
1 |
p. 213-220 |
artikel |
11 |
A Review of the European Community Regulatory Requirements for Expedited and Periodic ADR Reporting
|
Arnold, Barry D. C. |
|
1997 |
31 |
1 |
p. 181-186 |
artikel |
12 |
A Simple Three-Step Procedure for Parametric and Nonparametric Assessment of Bioequivalence
|
Vuorinen, Jouni |
|
1997 |
31 |
1 |
p. 167-180 |
artikel |
13 |
A Translational Approach to Education of Women on Bone Health Issues
|
DiGiorgio-Poll, Susan M. |
|
1997 |
31 |
1 |
p. 293-294 |
artikel |
14 |
Bar Coding during Clinical Trials: A Feasibility Study
|
Groenewoud, Gerhard |
|
1997 |
31 |
1 |
p. 229-235 |
artikel |
15 |
Clinical Research in China
|
Wong, Ellick |
|
1997 |
31 |
1 |
p. 93-95 |
artikel |
16 |
Clinical Trial Safety Surveillance in the New Regulatory and Harmonization Environment: Lessons Learned from the “Fialuridine Crisis”
|
Nickas, James |
|
1997 |
31 |
1 |
p. 63-70 |
artikel |
17 |
Curriculum Development: Training Primary Care Doctors to Diagnose and Treat Osteoporosis
|
Lipton, Steven E. |
|
1997 |
31 |
1 |
p. 279-286 |
artikel |
18 |
Development of a Human Growth and Osteoporosis Prevention Curriculum and Computer Program
|
Stern, Lawrence S. |
|
1997 |
31 |
1 |
p. 311-317 |
artikel |
19 |
Editor's Note
|
Teal, Thomas W. |
|
1997 |
31 |
1 |
p. 319 |
artikel |
20 |
Educating Young Women about Calcium
|
McMurray, Marybeth |
|
1997 |
31 |
1 |
p. 269-271 |
artikel |
21 |
FDA Inspection of Investigator Sites in Italy
|
Brunetti, N. |
|
1997 |
31 |
1 |
p. 187-191 |
artikel |
22 |
FDA Reform: Setting the Stage for Efforts to Reform the Agency
|
Kaitin, Kenneth I |
|
1997 |
31 |
1 |
p. 27-33 |
artikel |
23 |
Fears, Knowledge, and Perceptions of Osteoporosis among Women
|
Martin, Allison R. |
|
1997 |
31 |
1 |
p. 301-306 |
artikel |
24 |
Fibrodysplasia Ossificans Progressiva (FOP): The Value of Studying a Rare Disorder
|
Shore, Eileen M. |
|
1997 |
31 |
1 |
p. 273-277 |
artikel |
25 |
General Medical Practitioners' Approaches to Accessing Animate Sources of Drug Information*
|
Gerrett, David |
|
1997 |
31 |
1 |
p. 221-227 |
artikel |
26 |
Guest Editor's Note: First Annual Symposium on Curriculum Development in Osteoporosis
|
Giovenella, Albert J. |
|
1997 |
31 |
1 |
p. 265-267 |
artikel |
27 |
How to Improve the Medical Quality of the Coding Reports Based on Who-Art and Costart Use
|
Fizames, Christian |
|
1997 |
31 |
1 |
p. 85-92 |
artikel |
28 |
Opportunities in Downsizing and Reengineering for the Quality Assurance Unit
|
Hirsch, Allen F. |
|
1997 |
31 |
1 |
p. 259-263 |
artikel |
29 |
Orphan Drugs: The Current Situation in the United States, Europe, and Asia
|
Meyers, Abbey S. |
|
1997 |
31 |
1 |
p. 101-104 |
artikel |
30 |
Outsourcing Management in the Pharmaceutical Industry: The Early Stages at Four United States Companies
|
Daniel, Debbie A. |
|
1997 |
31 |
1 |
p. 111-118 |
artikel |
31 |
Patient Compliance of Women Taking Estrogen Replacement Therapy
|
Berman, Rayanne S. |
|
1997 |
31 |
1 |
p. 71-83 |
artikel |
32 |
Physical Rehabilitation of the Osteoporotic Patient
|
Fitzsimmons, Amy |
|
1997 |
31 |
1 |
p. 307-309 |
artikel |
33 |
Postapproval Changes in the United States—Is Life Getting Easier for Industry?
|
Dumitriu, Helene |
|
1997 |
31 |
1 |
p. 143-149 |
artikel |
34 |
Preparing for an FDA Advisory Committee Meeting
|
Pines, Wayne L. |
|
1997 |
31 |
1 |
p. 35-41 |
artikel |
35 |
Pricing and Reimbursement Issues in the European Economic Area
|
Hodges, Christopher J. S. |
|
1997 |
31 |
1 |
p. 251-258 |
artikel |
36 |
Recent Changes in Clinical Trial Authorization in Eastern Europe
|
Paál, Tamás L. |
|
1997 |
31 |
1 |
p. 151-155 |
artikel |
37 |
Results of a Data Imaging Pilot Project
|
Lawson, Marie E. |
|
1997 |
31 |
1 |
p. 193-196 |
artikel |
38 |
Specialized ANTI-HIV Testing: Expediting Preclinical Drug Development
|
Buckheit, Robert W. |
|
1997 |
31 |
1 |
p. 13-22 |
artikel |
39 |
Student Internships: Mutual Benefits in Osteoporosis Health Care and Research
|
Giovenella, Albert J. |
|
1997 |
31 |
1 |
p. 295-300 |
artikel |
40 |
Support and Illumination
|
Finney, David J. |
|
1997 |
31 |
1 |
p. 43-48 |
artikel |
41 |
The CDER Labeling and Nomenclature Committee: Structure, Function, and Process
|
Boring, Daniel L. |
|
1997 |
31 |
1 |
p. 7-11 |
artikel |
42 |
The Challenge of Auditing Clinical Laboratories
|
Desmet, Marian |
|
1997 |
31 |
1 |
p. 197-205 |
artikel |
43 |
The Challenge of Managing Quality Control/Quality Assurance for Loosely Structured and Virtual Biopharmaceutical Companies
|
Geigert, John |
|
1997 |
31 |
1 |
p. 97-100 |
artikel |
44 |
The Global Registration of Zyprexa™ (Olanzapine)
|
Worthen, Sue T. |
|
1997 |
31 |
1 |
p. 49-55 |
artikel |
45 |
The United States Orphan Drug ACT: Challenges and Success
|
Haffner, Marlene E. |
|
1997 |
31 |
1 |
p. 23-25 |
artikel |
46 |
Three Principles That Govern FDA Advertising and Promotion Regulation
|
Pines, Wayne L. |
|
1997 |
31 |
1 |
p. 137-142 |
artikel |
47 |
Validation of Clinical Laboratory Results: Discussion of Essential Validation Elements
|
Libeer, Jean-Claude |
|
1997 |
31 |
1 |
p. 243-250 |
artikel |