What is Pharmacovigilance?

Pharmacovigilance is a fancy word for the process of monitoring the effects of drugs and other pharmaceutical products.

The process starts with a drug or product being approved by the FDA, which means that it has been tested and found to be safe and effective. The drug company then needs to keep track of any adverse reactions or side effects that occur after the drug is on the market. This is done in order to determine if there are any long-term problems…

What is regulatory affairs?

Pharmaceutical regulatory affairs is a branch of health care that deals with the testing and approval of pharmaceuticals.

Pharmaceutical regulatory affairs is a branch of health care that deals with the testing and approval of pharmaceuticals. It is a highly regulated industry and there are many rules to follow in order to provide quality products. This includes…

What is Pharmacovigilance?

Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems. It also includes the entire process of collecting data on a medicine's safety profile.

Pharmacovigilance is a science that deals with the detection, assessment, understanding and prevention of adverse…

Overview of Clinical Research

Clinical research is the process of investigating the safety and effectiveness of new drugs, devices, and other treatments.

A clinical trial is a research study that tests new treatments or therapies that are intended to prevent, diagnose, or treat various conditions. It can also be used to test a new drug for safety and efficacy.

Clinical trials are usually…

What is Regulatory Affairs?

Regulatory affairs is a term used to describe the process of ensuring that a drug or medical device is safe and effective for use by humans. The regulatory affairs function includes many different roles and responsibilities, including clinical research, product approval, labelling/marketing/promotion, quality assurance, and post-market surveillance.

Regulatory…

What is Regulatory Affairs?

Drug Regulatory Affairs is the process of ensuring that drugs and medical devices are safe for public consumption. It includes the responsibility to ensure that all products are manufactured in accordance with current Good Manufacturing Practices (GMP), to maintain records, and to report adverse events.

Importance of regulatory Affairs

Drug Regulatory Affairs is…

What is Regulatory Affairs?

Drug Regulatory Affairs is the process of ensuring that drugs and medical devices are safe for public consumption. It includes the responsibility to ensure that all products are manufactured in accordance with current Good Manufacturing Practices (GMP), to maintain records, and to report adverse events.

Importance of regulatory Affairs

Drug Regulatory Affairs is…