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                             47 gevonden resultaten
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
                             47 gevonden resultaten
 
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