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Oral medicines for children in the European paediatric investigation plans

PloS one, 2014-06, Vol.9 (6), p.e98348-e98348

2014

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Practical Problems with Medication Use that Older People Experience: A Qualitative Study

Journal of the American Geriatrics Society (JAGS), 2014-12, Vol.62 (12), p.2339-2344

2014

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Opportunities for changes in the drug product design to enhance medication safety in older people: Evaluation of a national public portal for medication incidents

British journal of clinical pharmacology, 2020-10, Vol.86 (10), p.1946-1957

2020

Volltextzugriff (PDF)

Developing patient‐centric medicines for older people: Reflections from the draft EMA paper on the pharmaceutical development of medicines for use in the older population

British journal of clinical pharmacology, 2020-10, Vol.86 (10), p.2008-2013

2020

Volltextzugriff (PDF)

Safe and effective pharmacotherapy in infants and preschool children: importance of formulation aspects

Archives of Disease in Childhood, 2016-07, Vol.101 (7), p.662-669

2016

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Commentary on the EMA reflection paper on the pharmaceutical development of medicines for use in the older population

British journal of clinical pharmacology, 2022-02, Vol.88 (4), p.1500-1514

2022

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Methods of administering oral formulations and child acceptability

International journal of pharmaceutics, 2015-08, Vol.491 (1-2), p.261-267

2015

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Association between culture and the preference for, and perceptions of, 11 routes of medicine administration: A survey in 21 countries and regions

Exploratory research in clinical and social pharmacy, 2023-12, Vol.12, p.100378-100378, Article 100378

2023

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The availability and age‐appropriateness of medicines authorized for children in the Netherlands

British journal of clinical pharmacology, 2011-09, Vol.72 (3), p.465-473

2011

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Defining Patient Centric Pharmaceutical Drug Product Design

The AAPS journal, 2016-09, Vol.18 (5), p.1047-1055

2016

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Patients’ appropriateness, acceptability, usability and preferences for pharmaceutical preparations: Results from a literature review on clinical evidence

International journal of pharmaceutics, 2017-04, Vol.521 (1-2), p.294-305

2017

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Comments on the EMA draft guideline: Final steps towards a harmonized view between regulators and industry

International journal of pharmaceutics, 2013-11, Vol.457 (1), p.337-339

2013

Volltextzugriff (PDF)

The accuracy, precision and sustainability of different techniques for tablet subdivision: Breaking by hand and the use of tablet splitters or a kitchen knife

International journal of pharmaceutics, 2014-05, Vol.466 (1-2), p.44-51

2014

Volltextzugriff (PDF)

Results from a preliminary review of scientific evidence for appropriateness of preparations, dosage forms and other product design elements for older adult patients

International journal of pharmaceutics, 2015-01, Vol.478 (2), p.822-828

2015

Volltextzugriff (PDF)

Acceptability of different oral formulations in infants and preschool children

Archives of disease in childhood, 2013-09, Vol.98 (9), p.725-731

2013

Volltextzugriff (PDF)

Paediatric Drug Development and Formulation Design—a European Perspective

AAPS PharmSciTech, 2017-02, Vol.18 (2), p.241-249

2017

Volltextzugriff (PDF)

Effects of the pharmaceutical technologic aspects of oral pediatric drugs on patient-related outcomes: A systematic literature review

Clinical therapeutics, 2010-05, Vol.32 (5), p.924-938

2010

Volltextzugriff (PDF)

Regulatory incentives to ensure better medicines for older people: From ICH E7 to the EMA reflection paper on quality aspects

International journal of pharmaceutics, 2016-10, Vol.512 (2), p.343-351

2016

Volltextzugriff (PDF)

The EMA quality guideline on the pharmaceutical development of medicines for paediatric use

International journal of pharmaceutics, 2012-10, Vol.435 (2), p.132-134

2012

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Authors’ response to the letter from Kalleian Eserian et al

International journal of pharmaceutics, 2015-01, Vol.478 (2), p.682-683

2015

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Acceptability of different oral formulations in infants and preschool children

Archives of disease in childhood, 2013-10, Vol.98 (10), p.725

2013

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Demographics in the 2020s—Longevity as a challenge for pharmaceutical drug development, prescribing, dispensing, patient care and quality of life

British journal of clinical pharmacology, 2020-10, Vol.86 (10), p.1899-1903

2020

Volltextzugriff (PDF)

The development of a test battery to assess the hand–eye functions relevant in predicting easy and accurate tablet subdivision in older people: A pilot study

British journal of clinical pharmacology, 2020-10, Vol.86 (10), p.1969-1981

2020

Volltextzugriff (PDF)

The mechanisms of pharmacokinetic food-drug interactions – A perspective from the UNGAP group

European journal of pharmaceutical sciences, 2019-06, Vol.134, p.31-59

2019

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Age-Related Medicine

Pharmaceutics, 2019-04, Vol.11 (4), p.172

2019

Volltextzugriff (PDF)

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Oral medicines for children in the European paediatric investigation plans

Practical Problems with Medication Use that Older People Experience: A Qualitative Study

Opportunities for changes in the drug product design to enhance medication safety in older people: Evaluation of a national public portal for medication incidents

Developing patient‐centric medicines for older people: Reflections from the draft EMA paper on the pharmaceutical development of medicines for use in the older population

Safe and effective pharmacotherapy in infants and preschool children: importance of formulation aspects

Commentary on the EMA reflection paper on the pharmaceutical development of medicines for use in the older population

Methods of administering oral formulations and child acceptability

Association between culture and the preference for, and perceptions of, 11 routes of medicine administration: A survey in 21 countries and regions

The availability and age‐appropriateness of medicines authorized for children in the Netherlands

Defining Patient Centric Pharmaceutical Drug Product Design

Patients’ appropriateness, acceptability, usability and preferences for pharmaceutical preparations: Results from a literature review on clinical evidence

Comments on the EMA draft guideline: Final steps towards a harmonized view between regulators and industry

The accuracy, precision and sustainability of different techniques for tablet subdivision: Breaking by hand and the use of tablet splitters or a kitchen knife

Results from a preliminary review of scientific evidence for appropriateness of preparations, dosage forms and other product design elements for older adult patients

Acceptability of different oral formulations in infants and preschool children

Paediatric Drug Development and Formulation Design—a European Perspective

Effects of the pharmaceutical technologic aspects of oral pediatric drugs on patient-related outcomes: A systematic literature review

Regulatory incentives to ensure better medicines for older people: From ICH E7 to the EMA reflection paper on quality aspects

The EMA quality guideline on the pharmaceutical development of medicines for paediatric use

Authors’ response to the letter from Kalleian Eserian et al

Acceptability of different oral formulations in infants and preschool children

Demographics in the 2020s—Longevity as a challenge for pharmaceutical drug development, prescribing, dispensing, patient care and quality of life

The development of a test battery to assess the hand–eye functions relevant in predicting easy and accurate tablet subdivision in older people: A pilot study

The mechanisms of pharmacokinetic food-drug interactions – A perspective from the UNGAP group

Age-Related Medicine

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