In every country, a manufacturer of medicinal products for either human or veterinary use is required to operate in compliance with local legislation. In all EU Member States, legislation is approximated to the effect that they are committed to abide by the same standards. The candidate countries transpose the acquis into their national legislation, including the good manufacturing practice (GM...

Background: Safety, quality and effectiveness of Chinese patent medicine (CPM) are highly relevant to the manufacturing process. However, the level of manufacturing practice (GMP) for CPM as implemented in China is less reported in literatures. Therefore, the aim of this paper was to reveal the implementation status of GMP for CPM in China, in terms of implementation principle, implementation c...

Clinical research is like a foundation stone upon which a tower of evidence is erected which helps in the better understanding of the cause of the disease, improvement in the diagnosis treatment and mechanism of human biology (Trauter,1997). It is only the systematically carried out research which has made possible the increase in the life expectancy and decrease in human sufferings. While carr...

Just like Professor Ioana Grintescu, President of ROSEPN affirmed in the opening of the event, the purpose of this edition was to represent the memorable step in presenting some recommendations in the practical realization of some standards in the clinical nutrition so that, by the analysis of each stage and of the actual practices, to identify the progresses made and to propose future developm...

Informed parental consent reminds the health professional to respect parent autonomy with respect to their infant's health care. It involves at least four elements: information, assessment of understanding, assessment of capacity, and freedom to choose. Critical issues are training of staff, timing of approach, and quality and presentation of information. In the newborn period, additional probl...