This is a category for the course: Online and Full Time Post Graduate Diploma in Clinical Research
Skilled and trained professionals of data management help reduce the time-consuming processes from drug development to marketing stage. Data management Data Management is critical in clinical trial to lead and generate reliable, high-quality and statistically sound data by drastically reducing the number of stages involved in drug development process and marketing. Case report form (CRF) […]
Career stability and advancement is offered in the field of regulatory affairs to make a tangible difference in ensuring the safety and effectiveness of medical devices, pharmaceuticals, cosmetics, food and nutritional products available in the market. Regulatory affairs career Regulatory affairs is a profession developed with the desire to protect the public health as well as control safety […]
Clinical studies and trials play an important role in understanding cancer for developing innovative therapeutics and better diagnostics methods. These trials provide insights and assess on safe dosage or effectiveness of new ways of treatment, diagnosis and prevention. Clinical Trials for Cancer Clinical trials in cancer are research studies involving human volunteers designed by researchers […]
In 2008, SACRA (South African Clinical Research Association) estimated limited investment in internationally sponsored clinical trials conducted due to elongated time period for local regulatory approvals and insufficient suitable research sites. The Medicines Control Council (MCC) has recently made significant strides in reducing approval times and addressed deficiency associated with trial sites so as to […]
In contrast to intelligence displayed naturally by humans and animals, Artificial intelligence (AI) or Machine intelligence is demonstrated by machines. The genius created by AI tools these days affects every area of art, science and other professions including Pharmacovigilance systems. Pharmacovigilance is an iterative process like drug development where all stakeholders work collaboratively and proactively […]
Clinical research is a well established and prosperous field of science across the globe and is emerging as one of the major drivers of better healthcare delivery. It helps innovative drugs and interventions for prevention and treatment of various diseases to enter worldwide market. The increasing demand and booming market of clinical research provides better […]
In the United States and other foreign countries a pharmacist is allowed to practice clinical pharmacy. A statutory system exists wherein the diagnosis is carried out by doctors and then the patient is sent to the pharmacist who prescribes medication and charge for it. Pharmacists are highly salaried in the US where their average salary […]
A career in regulatory affairs is comparatively new and has come into existence because of governments pledging to protect the rights of their citizens by controlling the safety and efficacy of pharmaceutical products. Regulatory Affairs and Clinical Research go hand and hand, and to be a through professional, it is important for people who are […]
On the 26th of June 2013, the European Commission has adopted a proposal for regulation for the Conduct of Pharmacovigilance Activities in Respect of Medicinal Products for Human use. These changes in legislation will have an impact on the way assessment of drugs are carried out in both the stages of pre and post authorization, […]
Electronic data submission is the prospect of clinical studies and assessors will shortly have the legal authority to refuse submissions that do not comply with expectations. CDISC Standards are intended to overpower the impending problem of electronic data submission in coming future.