In my lecture I will focus on important developments in European drug regulation, such as personalized medicines, real world data, patient centricity and knowledge exchange. The lecture will acknowledge the long standing collaboration between the Dutch Medicines Evaluation Board and the department of Clinical Pharmacy and Pharmacology. It will also emphasize the need for collaboration between European regulators and other stakeholders to improve drug development and regulation
This paper presents an Irish research study currently being undertaken by the Pharmaceutical Regulat...
The current regulatory requirements offer accelerated assessment of innovative therapies in Europe. ...
Book synopsis: This unique collection brings together the work of social scientists, ethicists, ...
In my lecture I will focus on important developments in European drug regulation, such as personaliz...
Important discoveries by academic drug developers hold the promise of bringing innovative treatments...
Truly disruptive medicine innovation and new treatment paradigms tend to start in non-commercial res...
Over the last 10 years, there has been stagnation in the number of multinational drug trials in stro...
Dies lecture given by Prof.dr. Matthias Barz Professor fro Biopharmacy during the 447th Dies Natalis...
The PhD research ‘The Interplay of Global Standards and EU Pharmaceutical Regulation’ discusses the ...
Truly disruptive medicine innovation and new treatment paradigms tend to start in non-commercial res...
Regulatory science underpins the objective evaluation of medicinal products. It is therefore imperat...
Regulating drugs does not end when market access has been granted. Monitoring drugs over the life cy...
Efficiency and transparency of clinical drug research needs improvement In the Netherlands, approxim...
The Fifth European Symposium on Controlled Drug Delivery was held in Noordwijk aan Zee, The Netherla...
A monograph based on a seminar organised by The School of Chemistry & Pharmaceutical Sciences, Dubli...
This paper presents an Irish research study currently being undertaken by the Pharmaceutical Regulat...
The current regulatory requirements offer accelerated assessment of innovative therapies in Europe. ...
Book synopsis: This unique collection brings together the work of social scientists, ethicists, ...
In my lecture I will focus on important developments in European drug regulation, such as personaliz...
Important discoveries by academic drug developers hold the promise of bringing innovative treatments...
Truly disruptive medicine innovation and new treatment paradigms tend to start in non-commercial res...
Over the last 10 years, there has been stagnation in the number of multinational drug trials in stro...
Dies lecture given by Prof.dr. Matthias Barz Professor fro Biopharmacy during the 447th Dies Natalis...
The PhD research ‘The Interplay of Global Standards and EU Pharmaceutical Regulation’ discusses the ...
Truly disruptive medicine innovation and new treatment paradigms tend to start in non-commercial res...
Regulatory science underpins the objective evaluation of medicinal products. It is therefore imperat...
Regulating drugs does not end when market access has been granted. Monitoring drugs over the life cy...
Efficiency and transparency of clinical drug research needs improvement In the Netherlands, approxim...
The Fifth European Symposium on Controlled Drug Delivery was held in Noordwijk aan Zee, The Netherla...
A monograph based on a seminar organised by The School of Chemistry & Pharmaceutical Sciences, Dubli...
This paper presents an Irish research study currently being undertaken by the Pharmaceutical Regulat...
The current regulatory requirements offer accelerated assessment of innovative therapies in Europe. ...
Book synopsis: This unique collection brings together the work of social scientists, ethicists, ...