240 results on '"Klingmann, Ingrid"'
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2. Veränderungen durch die neue EU-Verordnung 536/2014 zu klinischen Prüfungen aus Patientensicht
3. A Composite Endpoint for Acceptability Evaluation of Oral Drug Formulations in the Pediatric Population
4. Validating a composite endpoint for acceptability evaluation of oral drug formulations in the pediatric population: a randomized, open-label, single dose, cross-over study.
5. Series: Public engagement with research. Part 3: Sharing power and building trust through partnering with communities in primary care research
6. Publishing clinical trial results in plain language: a clash of ethical principles?
7. Questionnaire Study to Investigate the Preferences of Children, Parents, and Healthcare Professionals for Different Formulations of Oral Medicinal Products.
8. A quality control system for ligand-binding assay of plasma renin activity: Proof-of-concept within a pharmacodynamic study
9. Orodispersible minitablets of enalapril for use in children with heart failure (LENA): Rationale and protocol for a multicentre pharmacokinetic bridging study and follow-up safety study
10. Toward A Regulatory Pathway for the Use of in Silico Trials in the CE Marking of Medical Devices
11. Question 1: How safe are ACE inhibitors for heart failure in children?
12. Consensus standards for introductory e-learning courses in human participants research ethics
13. Abstract 19995: Innovative Training Concept to Overcome Main Reasons for Failed Pediatric Clinical Trials and to Facilitate Successful Study Conduct and Recruitment
14. SPRINTT and the involvement of stakeholders: strategy and structure
15. Enalapril and Enalaprilat Pharmacokinetics in Children with Heart Failure Due to Dilated Cardiomyopathy and Congestive Heart Failure after Administration of an Orodispersible Enalapril Minitablet (LENA-Studies)
16. Alignment of Competencies to Address Inefficiencies in Medicines Development and Clinical Research: Need for Inter-Professional Education
17. Solving the Evidence Interpretability Crisis in Health Technology Assessment: A Role for Mechanistic Models?
18. The Role of EUPATI CH in Promoting Patient Involvement in Clinical Research: A Multi-Stakeholder Research Project
19. Using numerical modeling and simulation to assess the ethical burden in clinical trials and how it relates to the proportion of responders in a trial sample
20. ICH: Strengths, Weaknesses, and Future Tasks
21. A composite endpoint for acceptability evaluation of oral drug formulations in the pediatric population
22. Referee report. For: Twelve months into a feasibility trial: reflections on three experiences of public and patient involvement in research [version 1; peer review: 3 approved with reservations]
23. Referee report. For: Twelve months into a feasibility trial: reflections on three experiences of public and patient involvement in research [version 2; peer review: 3 approved]
24. Ethical Challenges in Clinical Research at Both Ends of Life
25. Efficacy of the long-acting nitro vasodilator pentaerithrityl tetranitrate in patients with chronic stable angina pectoris receiving anti-anginal background therapy with beta-blockers: a 12-week, randomized, double-blind, placebo-controlled trial
26. Simulation Training to Improve Informed Consent and Pharmacokinetic/Pharmacodynamic Sampling in Pediatric Trials
27. Cross-Border Access to Clinical Trials in the EU: Exploratory Study on Needs and Reality
28. Evolution of the Development of Core Competencies in Pharmaceutical Medicine and Their Potential Use in Education and Training
29. A quality control system for ligand-binding assay of plasma renin activity: Proof-of-concept within a pharmacodynamic study
30. A comprehensive quality control system suitable for academic research: application in a pediatric study
31. The Specialist in Medicines Development (SMD) as a Vocational Program in Pharmaceutical Medicine: The Japanese and Italian Experience
32. Simultaneous Semi-Mechanistic Population Pharmacokinetic Modeling Analysis of Enalapril and Enalaprilat Serum and Urine Concentrations From Child Appropriate Orodispersible Minitablets
33. Model-dependent pharmacokinetic analysis of enalapril administered to healthy adult volunteers using orodispersible minitablets for use in pediatrics
34. A 6-month process for planning multinational clinical trials: what happens in the six months before a trial is just as important as what happens during the trial. (Focus On Europe)
35. Exploratory Medicines Development
36. How safe are ACE inhibitors for heart failure in children?
37. Relative Bioavailability of Enalapril Administered as Orodispersible Minitablets in Healthy Adults
38. Pharmacotherapeutic management of paediatric heart failure and ACE-I use patterns: a European survey
39. EUPATI Guidance for Patient Involvement in Medicines Research and Development (R&D); Guidance for Pharmaceutical Industry-Led Medicines R&D
40. Efficacy, safety and tolerability of progesterone vaginal pessaries versus progesterone vaginal gel for luteal phase support after in vitro fertilisation: a randomised controlled trial.
41. Relative Bioavailability of Enalapril Administered as Orodispersible Minitablets in Healthy Adults.
42. EUPATI and Patients in Medicines Research and Development: Guidance for Patient Involvement in Ethical Review of Clinical Trials
43. EUPATI Guidance for Patient Involvement in Medicines Research and Development: Health Technology Assessment
44. EUPATI and Patients in Medicines Research and Development: Guidance for Patient Involvement in Regulatory Processes
45. EUFEMED London Conference 2017: Exploratory Medicines Development: Innovation and Risk Management
46. Question 1: How safe are ACE inhibitors for heart failure in children?
47. Acute effects and after-effects of acoustic coordinated reset neuromodulation in patients with chronic subjective tinnitus
48. Position statement from the European Board and College of Obstetrics & Gynaecology (EBCOG)
49. DEVELOPMENT AND ESTABLISHMENT OF A QUALITY-FRAMEWORK FOR THE LENA PROJECT
50. A Risk-based Approach to Patient Information?
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