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                             14 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Access versus evidence: The regulators’ dilemma Schilsky, Richard L
2018
15 3 p. 240-242
artikel
2 A new modeling and inference approach for the Systolic Blood Pressure Intervention Trial outcomes Yang, Song
2018
15 3 p. 305-312
artikel
3 Bayesian comparative effectiveness study of four consensus treatment plans for initial management of systemic juvenile idiopathic arthritis: FiRst-Line Options for Systemic juvenile idiopathic arthritis Treatment (FROST) Nigrovic, Peter A
2018
15 3 p. 268-277
artikel
4 Beyond total treatment effects in randomised controlled trials: Baseline measurement of intermediate outcomes needed to reduce confounding in mediation investigations Landau, Sabine
2018
15 3 p. 247-256
artikel
5 Expedited and facilitated drug evaluations and evidence of benefit and risk: The cup is half-full Califf, Robert M
2018
15 3 p. 235-239
artikel
6 Expedited approval programs at the Food and Drug Administration Begg, Colin B
2018
15 3 p. 217-218
artikel
7 Expediting drug development for serious illness: Trade-offs between patient access and certainty Woodcock, Janet
2018
15 3 p. 230-234
artikel
8 Increasing the use of mobile technology–derived endpoints in clinical trials Herrington, William G
2018
15 3 p. 313-315
artikel
9 LIBERTI: A SMART study in plastic surgery Hibbard, Jonathan C
2018
15 3 p. 286-293
artikel
10 Prevalence and reporting of recruitment, randomisation and treatment errors in clinical trials: A systematic review Yelland, Lisa N
2018
15 3 p. 278-285
artikel
11 Reporting non-adherence in cluster randomised trials: A systematic review Agbla, Schadrac C
2018
15 3 p. 294-304
artikel
12 The reporting of harms in publications on randomized controlled trials funded by the “Programme Hospitalier de Recherche Clinique,” a French academic funding scheme Favier, Romain
2018
15 3 p. 257-267
artikel
13 The US Food and Drug Administration’s expedited approval programs: Addressing premarket flexibility with enhanced postmarket evidence generation Wallach, Joshua D
2018
15 3 p. 243-246
artikel
14 The US Food and Drug Administration’s expedited approval programs: Evidentiary standards, regulatory trade-offs, and potential improvements Wallach, Joshua D
2018
15 3 p. 219-229
artikel
                             14 gevonden resultaten
 
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