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                             38 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Advancing Rheumatology Care Through Machine Learning Hügle, Thomas

2 p. 87-96
artikel
2 A Principles Framework for Digital Provision of Medical Information for Healthcare Professionals Mohamed, Susan

2 p. 103-109
artikel
3 A Retrospective Review of Serious Adverse Drug Reaction Reports in the Nigerian VigiFlow Database from September 2004 to December 2016 Ogar, Comfort Kunak

2 p. 145-157
artikel
4 A Transition to Targeted or ‘Smart’ Vaccines: How Understanding Commensal Colonization Can Lead to Selective Vaccination Beitelshees, Marie

2 p. 95-102
artikel
5 Cannabidiol and Other Phytocannabinoids as Cancer Therapeutics Nahler, Gerhard

2 p. 99-129
artikel
6 Clinical Presentations of Drug-Induced Hyperprolactinaemia: A Literature Review Junqueira, Daniela R.

2 p. 153-166
artikel
7 Considerations for Effective Communication of Medical Information Power, Eddie G. M.

2 p. 97-101
artikel
8 COVID-19: Reasons for Guarded Optimism Snell, Noel

2 p. 67-69
artikel
9 Decentralisation in Clinical Trials and Patient Centricity: Benefits and Challenges Sinha, Shubhadeep D.

2 p. 109-120
artikel
10 Digital Therapies (DTx) as New Tools within Physicians’ Therapeutic Arsenal: Key Observations to Support their Effective and Responsible Development and Use Bélisle-Pipon, Jean-Christophe

2 p. 121-127
artikel
11 Drugs in Clinical Development for HIV: Summary and Table
2 p. 105-111
artikel
12 Drugs in Clinical Development for Renal Cancer Summary and Table
2 p. 75-84
artikel
13 Effect of Caffeine Consumption on Cardiovascular Disease: An Updated Review Khiali, Sajad

2 p. 139-151
artikel
14 Emergency Approval Mechanisms for Human Vaccines in India Mehrotra, Nidhi

2 p. 121-132
artikel
15 Evaluating the Effectiveness of Apixaban Additional Risk Minimisation Measures Using Surveys in Europe Mayall, Steve

2 p. 123-135
artikel
16 Female Problems: Women’s Health Mustn’t be Ghettoized in the Uterus Pitts, Peter J.

2 p. 75-77
artikel
17 Forum
2 p. 117-127
artikel
18 Forum
2 p. 117-128
artikel
19 Impact of Advantage in Tumor Response on the Correlation Between Progression-Free Survival and Overall Survival: Meta-Analysis of Clinical Trials in Patients with Advanced Non-Small Cell Lung Cancer Yoshida, Yosuke

2 p. 81-92
artikel
20 Klaus Rose. Considering the Patient in Pediatric Drug Development: How Good Intentions Turned into Harm Striano, Pasquale

2 p. 137-138
artikel
21 Major Pharmaceutical Conferences and Courses: June to July 2022
2 p. 143-145
artikel
22 Major Pharmaceutical Conferences and Courses: June to July 2021
2 p. 139-141
artikel
23 Major Pharmaceutical Conferences and Courses: June to July 2023
2 p. 167-170
artikel
24 Meaningful Within-Patient Change in Subjective Total Sleep Time in Patients with Insomnia Disorder: An Analysis of the Sleep Diary Questionnaire Using Data from Open-Label and Phase III Clinical Trials Phillips-Beyer, Andrea

2 p. 133-144
artikel
25 Medical Affairs and Innovative Medicinal Product Strategy Development Krendyukov, Andriy

2 p. 71-82
artikel
26 Medical Affairs Transformation in Specialty Pharma: Next-Level Collaboration at the Core Fulford-Smith, Antony

2 p. 63-69
artikel
27 Medical Information Delivering Improved Customer Experience: A Guide Guillot, Pete

2 p. 111-119
artikel
28 Medicines Regulatory Science Expertise in Africa: Workforce Capacity Development and Harmonisation Activities Towards the Establishment of the African Medicines Agency Ncube, Bakani Mark

2 p. 83-97
artikel
29 Physician Awareness of the Safe Use of Cyproterone Acetate in Europe: A Survey on the Effectiveness of Additional Risk Minimization Measures Sweeney, Carolyn

2 p. 145-156
artikel
30 Potential of Artificial Intelligence to Accelerate Drug Development for Rare Diseases Napolitano, Giulio

2 p. 79-86
artikel
31 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.

2 p. 89-98
artikel
32 Quantitative Methods for Safety Monitoring of Rare Serious Adverse Events Duke, Susan P.

2 p. 113-118
artikel
33 Regulatory Approval Scenario of Biosimilars in Pediatric Patients in the United States and European Union Radhakrishna, Swetha

2 p. 93-112
artikel
34 The Carbon Costs of In-Person Versus Virtual Medical Conferences for the Pharmaceutical Industry: Lessons from the Coronavirus Pandemic Gattrell, William T.

2 p. 131-142
artikel
35 The conect4children (c4c) Consortium: Potential for Improving European Clinical Research into Medicines for Children Turner, Mark A.

2 p. 71-79
artikel
36 The Qualitative Value of Facilitated Regulatory Pathways in Europe, USA, and Japan: Benefits, Barriers to Utilization, and Suggested Solutions Bujar, Magdalena

2 p. 113-122
artikel
37 Using Patient Perspectives to Inform Better Clinical Trial Design and Conduct: Current Trends and Future Directions Faulkner, Stuart D.

2 p. 129-138
artikel
38 Why Oncology Global Safety Teams Should Develop the Safety Section of the Study’s Target Product Profile (TPP) Kieffer, Michael E.

2 p. 97-108
artikel
                             38 gevonden resultaten
 
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