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 |