Clinical trials and pharmacovigilance are integral and important to drug development and post marketing activities during the actual use of the drug. Courses in Clinical Research and Pharmacovigilance create large number of job opportunities by training and developing skills in professionals to the level expected in the industry. Advanced PG Diploma in Clinical Research & […]
Pharmacovigilance requires strong links with regulators to ensure that authorities are well briefed on safety issues to enforce regulatory action in the future. Post market surveillance The value of post-market surveillance to protect consumers defines and clarifies the professional regulatory role in communicating product safety as technology continues to increase data accessibility. The cornerstone of […]
Diverse opportunities are available to pharmacists for independent work with broad range of roles in clinical research. Pharmacists use number of skills and play important role in areas of clinical trial operations, medical writing, pharmacovigilance, researchand development and medico-marketing.
Safety and efficacy are mostly the two things to be concerned around the usage of a drug product and, we might contemplate if we have anyone monitoring that? Well yes, its Pharmacovigilance. Pharmacovigilance is the science and the actions related to detection, assessment, understanding and prevention of adverse effects or any other drug-related problem. In […]
Clinical Pharmacology is defined as the study of the effects of drugs in human beings and Pharmacoepidemiology falls under the category of Clinical Pharmacology.
This short post is an attempt to cover careers pertaining to Pharmacovigilance. One interested in pursuing this career would come across a term called as “Drug Safety Associate”. So who exactly is a Drug Safety Associate and what are the job responsibilities of such a position holder? The roles and responsibilities of a Drug Safety […]
Pharmacovigilance is the practice of using scientific methods to track, record and analyze the effects of pharmaceuticals, with a focus on determining and maintaining the quality and safety of consumer medicines. Every year a record number of people die due to Adverse Drug Reactions (ADR). It becomes increasingly important for all members of clinical trial […]
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, […]
Pharmacovigilance is the division of science relating to to the detection, inference, understanding and evasion of unfavorable effects, chiefly long and short term detrimental effects associated with medicines. In broader sense, it deals with collection, monitoring, estimating and analyzing information from medical service providers and patients on the evil effects of allopathic, biological and herbal medications and unconventional medicines. […]
The universal health challenge of highlighting drug safety by protecting the public confidence has become progressively more intricate. Drug discovery companies are forced to employ dedicated staff to take the responsibility for pharmacovigilance.