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                             33 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 An Industry Survey on Managing the Pharmacovigilance System Master File in a Global Environment: The Need for a Pragmatic Approach Lavery, Clare

4 p. 233-245
artikel
2 A Structured Methodology to Assess Safety Signal Strength and Inform Causality Assessment Sullivan, Tim

4 p. 215-222
artikel
3 Biosimilar Uptake: The Importance of Healthcare Provider Education Oskouei, Sonia Tadjalli

4 p. 215-224
artikel
4 Challenges Faced by the Biopharmaceutical Industry in the Development and Marketing Authorization of Biosimilar Medicines in BRICS-TM Countries: An Exploratory Study Rahalkar, Hasumati

4 p. 235-251
artikel
5 Clinical Quality in Cancer Research: Strategy to Assess Data Integrity of Germline Variants Inferred from Tumor-Only Testing Sequencing Data Ménard, Timothé

4 p. 225-233
artikel
6 Correction to: Providing Patients with Critical or Life-Threatening Illnesses Access to Experimental Drug Therapy: A Guide to Clinical Trials and the US FDA Expanded Access Program Speers, Marjorie A.

4 p. 295
artikel
7 Current Prospects of Molecular Therapeutics in Head and Neck Squamous Cell Carcinoma Devaraja, K.

4 p. 269-289
artikel
8 Current Status and Challenges of Pharmacovigilance of Traditional Medicines in French-Speaking West African (UEMOA) Countries Ouoba, Kampadilemba

4 p. 305-318
artikel
9 Embedding Patient-Centricity by Collaborating with Patients to Transform the Rare Disease Ecosystem Sharma, Rohita

4 p. 265-273
artikel
10 EU Compassionate Use Programmes (CUPs) Sou, Hélène

4 p. 223-229
artikel
11 Evaluation of Drug Lags in Development Initiation, New Drug Application and Approval Between Japan and the USA and the Impact of Local Versus Multi-regional Clinical Trials Ushijima, Satoshi

4 p. 253-260
artikel
12 Evaluation of the Performance of the Gulf Cooperation Council Centralised Regulatory Review Process: Strategies to Improve Product Authorisation Efficiency and Quality Hashan, Hajed M.

4 p. 223-231
artikel
13 Evolving Communication with Healthcare Professionals in the Pharmaceutical Space: Current Trends and Future Perspectives Krendyukov, Andriy

4 p. 247-256
artikel
14 Forum
4 p. 279-290
artikel
15 Forum
4 p. 229-239
artikel
16 Global Landscape of Benefit–Risk Considerations for Medicinal Products: Current State and Future Directions Waschbusch, Max

4 p. 201-213
artikel
17 IL-6 Inhibitors in the Treatment of Serious COVID-19: A Promising Therapy? Atal, Shubham

4 p. 223-231
artikel
18 Interpersonal Values of Patients Participating in Phase II–III Clinical Trials: Implications for Clinical Trial Representativeness Gouveia, Rita

4 p. 319-329
artikel
19 Is Psoriasis Treatment a Risk Factor for Inflammatory Bowel Disease? Nehring, Piotr

4 p. 257-262
artikel
20 Major Pharmaceutical Conferences and Courses
4 p. 291-293
artikel
21 Major Pharmaceutical Conferences and Courses: October to November 2022
4 p. 261-264
artikel
22 Major Pharmaceutical Conferences and Courses: October to November 2021
4 p. 261-265
artikel
23 Major Pharmaceutical Conferences and Courses: October to November 2023
4 p. 335-341
artikel
24 Meaningful Within-Patient Change on the Insomnia Daytime Symptoms and Impacts Questionnaire (IDSIQ): Analysis of Phase III Clinical Trial Data of Daridorexant Phillips-Beyer, Andrea

4 p. 291-303
artikel
25 Patent Cliffs in the Era of Complex Therapies and Biologics Sabatini, Marco T.

4 p. 271-278
artikel
26 Potential Channeling Bias in the Evaluation of Cardiovascular Risk: The Importance of Comparator Selection in Observational Research Li, Hu

4 p. 247-259
artikel
27 Preparing for the Next Normal: Transformation in the Role of Medical Affairs Following the COVID-19 Pandemic Ghosh, Romik

4 p. 197-202
artikel
28 Tackling Counterfeit Drugs: The Challenges and Possibilities Pathak, Ranjana

4 p. 281-290
artikel
29 75th Annual Meeting of the American Academy of Neurology (AAN 2023) Pochon, Sue

4 p. 331-334
artikel
30 The Central Role of Ethics in Medical Affairs Practice Naraynassamy, Carl

4 p. 275-279
artikel
31 The Emergency Use Authorization of Pharmaceuticals: History and Utility During the COVID-19 Pandemic Tran, Allan

4 p. 203-213
artikel
32 The NIMH ‘Fast-Fail Trials’ (FAST) Initiative: Rationale, Promise, and Progress Grabb, Margaret C.

4 p. 233-245
artikel
33 Using Data from the Canadian Post-marketing Spontaneous Pharmacovigilance System for Drug Safety Research: A Feasibility Study Akinola, Samuel

4 p. 263-269
artikel
                             33 gevonden resultaten
 
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