This is a category for pharmacovigilance courses
What is GVP? Good Pharmacovigilance Practices (GVP) are a set of measures drawn up to facilitate the performance of pharmacovigilance in the European Union (EU). GVP apply to marketing-authorisation holders, the European Medicines Agency (EMA) and medicines regulatory authorities in EU Member States. They cover medicines authorised centrally via the Agency as well as medicines authorised at national […]
In every interview that you might attend, you always wish to know the questions beforehand. However, you should keep in mind that the panel sitting in front of you is experienced and can go a step higher if you can steer clear from their simple volleys. No list of questions or guide is perfect but […]
Safety is what an individual seeks. From our day to day living and more importantly in the drugs we consume for our benefits. It would be surprising to know that the drugs/medicines we consume at times can cause adverse reactions in certain individuals. This is where Pharmacovigilance plays a very important role in detecting, analyzing, […]
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 […]
Scope of Pharm.D in India Indian pharmacy education took a big leap in the year 2008 with The Pharmacy Council of India recognizing the Pharm.D program. This was a move to standardize pharmacy education in India and make it at par with international standards. Numerous universities and colleges in India have launched the Pharm.D program; […]
Tags: Careers in Pharmacovigilance, Pharmacovigilance Training, Online Pharmacovigilance Courses Pharmaceuticals is regarded as an evergreen industry. Drug safety or Pharmacovigilance is at the center stage of new drug development as well as postmarketing evaluation of approved drugs and devices. This creates a very vital niche for the pharmacovigilance industry inside the much larger and expanding pharmaceutical business. It would […]
‘All drugs need to be safe and efficacious’ is an ideal goal and the objective of the pharmaceutical industry, researchers and the regulatory agencies is to come closer to this goal as much as possible. In the public health scenario the concepts of drug safety takes a higher priority due to a wider application of […]
Narrative writing is an important part of Pharmacovigilance and in patient safety as well. Usually patient narratives are written in case of Adverse Events and Serious Adverse Events including deaths. Patient narratives form a very important part of clinical study reports and all other post marketing activities. In case of a Serious Adverse Event it […]
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 […]
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 […]