Good Clinical Practices sets the principles for drug safety information and news on adverse drug reactions, describing that the clinical study’s sponsor is answerable for the enduring safety evaluation of the novel drugs being explored. Along with this, the Good Clinical Practices must quickly inform all relevant clinicians/ethics committees and the applicable regulatory authority of […]
Pharmaceutical medicine is a much valued scientific discipline deals with the discovery/invention, development, assessment, registration, scrutinize and medical aspects of commercialization of medicines for the benefit of sufferers and the health of the human population. Pharmaceutical medicine training programs are gaining ground and the traditional universities are now focussing on interdisciplinary approach of handling the […]
Healthcare management can be described as the utilization of medical and information technology, as well as administrative and managerial skills, to make sure the finest delivery of healthcare services.
Translational medicine can be defined as investigations in human subjects which describe the biology of disease and offer the scientific basis for development of novel or effective therapies for human disease based on interventional epidemiology. It amalgamates research from the fundamental, social and political sciences with the objective of fine tuning the patient care and […]
Brazil is a nation of continental magnitude with extensive social and provincial inequalities. Health care in Brazil is sponsored by the Government. The Ministry of Health is accountable for public healthcare services, government healthcare undertakings and medical services. Majority of the private hospitals in Brazil have exceptional healthcare facilities and Brazil is one of the […]
Why courses in Pharmacovigilance have become obligatory? Why are the personnel trained in pharmacovigilance are in high demand? The reason behind is not just a meager comfort but a compulsion from every bodies stand point!
The Clinical Research Coordinator (CRC) is a dedicated clinical professional allied with and under the command of a Principal Investigator (PI). Despite the fact that the Principal Investigator is chiefly responsible for the general trial design, conduct, and organization of the clinical study, the CRC assists, and handle the day-to- day activities pertaining to clinical […]
A well trained professional made of sterner stuff can only execute clinical research associate job efficiently and competently. Keeping in view the professional demands, a CRA must have a strong grounding in ethical considerations, international regulatory requirements, clinical trial conduct in agreement with global GCP and an appreciable understanding of allied activities like data management, […]
Managing a healthcare organization now-a-days is comparable to managing a total city. It’s a vibrant environment of specialized clusters that have both direct and indirect associations with one another, and seldom, contending interests. To direct such an organization needs vigilant budgeting, strong decision-making, and above all in addition, the capability to sustain the esteem and […]
Clinical trials are performed in a methodically regulated process following some pertinent guidelines formulated by by the International Conference on Harmonization (ICH), which is led by the EU, USA, and Japan. Clinical research education and training is made implicitly mandatory by ICH-GCP highlighting the need for only well educated and qualified professionals to take part […]