Pharmacy clinical research in Bangalore

Pharmacy clinical research in Bangalore

Pharmacy clinical research in Bangalore

Generally speaking, pharmacovigilance is the science of collecting, monitoring, researching, assessing and evaluating information from healthcare providers and patients on the adverse effects of medications, biological products, herbalism and traditional medicines with a view to: identifying new information about hazards associated with medicines preventing harm to patients.

It aims at detection, assessment and prevention of adverse effects and other medication related problems. This one year part time course is designed to impart the knowledge of regulatory requirements of drug safety monitoring for various countries, train the students on management of pharmacovigilance projects in an organization, drug safety data development during pre-clinical and clinical phases of drug development and during post approval period

Pharmacovigilance is particularly concerned with adverse drug reactions, or ADRs, which are officially described as: "A response to a drug which is noxious and unintended, and which occurs at doses normally used for the prophylaxis, diagnosis or therapy of disease, or for the modification of physiological function."

Pharmacovigilance is gaining importance for doctors and scientists as the number of stories in the mass media of drug recalls increases.

Because clinical trials involve several thousand patients at most; less common side effects and ADRs are often unknown at the time a drug enters the market. Even very severe ADRs such as liver damage are often undetected because study populations are small. Post marketing pharmacovigilance uses tools such as data mining and investigation of case reports to identify the relationships between drugs and ADRs.

Pharmaceutical companies are required by law in all countries to perform clinical trials, testing new drugs on people before they are made generally available. The manufacturers or their agents usually select a representative sample of patients for whom the drug is designed at most a few thousand along with a comparable control group. The control group may receive a placebo and/or another drug that is already marketed for the disease.

The purpose of clinical trials is to discover:

If a drug works and how well

If it has any harmful effects, and

Its benefit-harm-risk profile - does it do more good than harm, and how much more? If it has a potential for harm, how probable and how serious is the harm?

We always provide an in-depth knowledge and training in the applied fields of clinical research, medicine, pharmaceuticals and biotechnology in a unique amalgamated environment of academy & industry.

For more information on Pharmacy clinical research in Bangalore you can visit http://www.czinfosolutions.com

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