Introduction

In simpler words, clinical research is a type of investigation that covers all areas of treatment, diagnosis, prevention and curing diseases. It could also be said that majority of practicing doctors and professionals would be familiar more with the results of a clinical trial than medical journals. In order to start your journey as a clinical research professional, get to know more about…

The Regulatory Affairs Knowledge is a must for pharmaceutical companies. Regulatory Affairs is a multifaceted field that deals with the regulation of medicinal products, such as drug development and marketing, medical devices, and other healthcare products.

The Regulatory Affairs Knowledge is an important part of the pharmaceutical industry. It deals with the regulation of medicinal products, such as drug development and marketing, medical devices, and other healthcare products.…

What is a regulatory specialist?

Regulatory specialists are people who work in the regulatory space. They help ensure compliance with regulations and standards, and they help to design new regulatory frameworks. Pharmacovigilance Courses in India

They could be working for a public sector organisation, such as a government department or agency, or in the private sector for a company that is…

What is pharmacovigilance?

Pharmacovigilance is the process of detecting, assessing, and reducing the risks of adverse effects associated with pharmaceutical products.

Pharmacovigilance is a process that aims to reduce risks from adverse effects of pharmaceutical products. It is a continuous cycle that begins when the drug is marketed and continues as long as the product is available in the…

What is pharmacovigilance?

Pharmacovigilance is the process of detecting, assessing, and reducing the risks of adverse effects associated with pharmaceutical products.

Pharmacovigilance is a process that aims to reduce risks from adverse effects of pharmaceutical products. It is a continuous cycle that begins when the drug is marketed and continues as long as the product is available in the…

Introduction to Pharmacovigilance

Pharmacovigilance is an important part of the drug development process, and it ensures that the benefits of the drugs outweigh the risks. It includes monitoring a drug's safety after it has been approved for marketing, and identifying any adverse effects that may not have been known before.

Pharmacovigilance is one of the most important parts of drug…

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…