Good manufacturing practice (GMP) is applied to the manufacture of immunological veterinary medicinal products (IVMPs) in a number of regions around the world. Within the European Union (EU) there are well-established requirements for GMP in the manufacture of IVMPs. Maintaining GMP when producing IVMPs is important because there are particular risks associated with their manufacture. These ris...

Abstract Background All currently available products for diagnosis and therapy of type I allergies are protein extracts from allergenic source material. The extracted proteins have different properties their structure is differently labile to temperature variations. Despite various pharmaceutical formulations increase product stability, with few exceptions, allergen must be refrigerated ensure ...

The work environment is one of the most important factors in production. In this paper, a study was conducted on MSMEs to determine safety and health producing products. Specifically, see deviation application GMP MSME. subjects were 30 involved research from Binjai Municipalities. This uses qualitative analysis method that aims evaluate level 14 aspects find out understanding GMP. results show...

INTRODUCTION The Ethics Committees (EC) are established to safeguard the safety and rights of the subjects participating in a research study. No formal training about Ethics Committee is given to the medical students in undergraduate and post graduate education as a part of curriculum. AIMS AND OBJECTIVES To study the awareness about the composition and functioning of EC amongst the medical t...

Identity theft is the fastest growing crime in the 21 century. This paper investigates firstly what well-known e-commerce organizations are communicating on their websites to address this issue. For this purpose we analyze secondary data (literature and websites of ten organizations). Secondly we investigate the good practice in this area and recommend practical steps. The key findings are that...

The Guideline for Good Clinical Practice (GCP) of the International Conference of Harmonisation (ICH) is an international standard for the ethical and scientific quality of the designing, conducting, recording and reporting of trials that involve the participation of human subjects. Today, most regulators and funding agencies follow the ICH guidelines. These were drawn up by a small number of r...