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                             28 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A Consultant's View on the Role of Bayesian Differential Diagnosis in the Safety Assessment of Pharmaceuticals Naranjo, Claudio A.
1992
26 4 p. 593-601
artikel
2 An Expert System for Prediction of Chemical Toxicity Hickey, James P.
1992
26 4 p. 487-495
artikel
3 An Industry Perspective on the State of Confusion in International ADR Reporting: Current Requirements and Attempts at Standardization Gordon, Arnold J.
1992
26 4 p. 573-581
artikel
4 Armor: ICI's Automated Tracking System for Adverse Events from Clinical Trials Klinger, Elizabeth J.
1992
26 4 p. 537-543
artikel
5 Causality Assessment in the European Pharmaceutical Industry: Presentation of the Preliminary Results of a New Method Bénichou, Christian
1992
26 4 p. 589-592
artikel
6 Clinical Trial Adverse Drug Experience Reporting Requirements in the Major Countries and a Simplified Approach toward Meeting These Requirements Talbott, Max W.
1992
26 4 p. 519-525
artikel
7 Computer-Aided Assessment of the Adverse Effects of Antiepileptic Drugs Mabry, Michael E.
1992
26 4 p. 505-517
artikel
8 Data Management Team-Driven Approach to Handling International Clinical Data Hudson, Ronald Carlisle
1992
26 4 p. 659-665
artikel
9 Did My Drug Cause This? a Biostatistical Perspective Von Tress, Mark S.
1992
26 4 p. 565-572
artikel
10 Did My Drug Cause This? an Academic Perspective Knodel, Leroy C.
1992
26 4 p. 559-564
artikel
11 EEC Pharmacovigilance and the Pharmaceutical Industry: Common Market, Common Rules? Bénichou, Christian
1992
26 4 p. 473-476
artikel
12 Good Clinical Practice: EC Expectations Education, Self-Regulation, or Imposition? Jefferys, David B.
1992
26 4 p. 609-613
artikel
13 Guest Editor's Note Herman, Raymond L.
1992
26 4 p. 471
artikel
14 Issues with Causality Assessment: A Personal Perspective Schneiweiss, Fred
1992
26 4 p. 549-551
artikel
15 Managing Adverse Reaction Information Mann, Ronald D.
1992
26 4 p. 583-587
artikel
16 Market Failure, Information Imperfections, and Cost-Effectiveness Analysis Hoerger, Thomas J.
1992
26 4 p. 647-654
artikel
17 New Designs for Stability Testing Programs: Matrix or Factorial Designs. Authorities' Viewpoint on the Predictive Value of Such Studies Helboe, Per
1992
26 4 p. 629-634
artikel
18 Predicting Anaphylactoid Reactions Based on Costart Terms Rinsler, Steven S.
1992
26 4 p. 497-504
artikel
19 Reasonable Possibility: Causality and Postmarketing Surveillance Johnson, Joyce M.
1992
26 4 p. 553-558
artikel
20 Software Survey Section 1992
26 4 p. i-iv
artikel
21 Strategies for Successfully Managing Pharmaceutical Research and Development in the 1990s Drews, Jürgen
1992
26 4 p. 635-645
artikel
22 The Glaxo International Postmarketing Surveillance System: Present and Future Phillips, George
1992
26 4 p. 527-535
artikel
23 The Italian Multicenter Trial on Prevention and Treatment of Benzodiazepine Withdrawal: Methodology and Pretrial Cassano, Giovanni B.
1992
26 4 p. 615-627
artikel
24 The Passport to Drug Approval Teijgeler, C. A.
1992
26 4 p. 655-657
artikel
25 The Pharmaceutical Industry on the Continent — A 10-Year Perspective since Morges Venulet, Jan
1992
26 4 p. 603-608
artikel
26 The Who Database—I Edwards, I. Ralph
1992
26 4 p. 477-480
artikel
27 The Who Database—II Edwards, I. Ralph
1992
26 4 p. 481-486
artikel
28 WAES*NET — Merck's International AE Reporting System Sromovsky, Judith A.
1992
26 4 p. 545-548
artikel
                             28 gevonden resultaten
 
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