Got Stuck? Join Hands with Turacoz to Streamline your Pharmacovigilance Process

Whenever there is a new drug on the market the biggest question surrounding it is about its safety and any possible adverse effects. Drugs are created for the safety and betterment of human lives, so it is very important to be sure of the usage of the drug, its side-effects, etc.

This is where Pharmacovigilance comes into the picture. If you are a pharma company/drug manufacturer, you might want someone to offer you with pharmacovigilance support.

Pharmacovigilance deals with 2 main aspects:

v  Safety: how safe is the drug for consumption & how they work on patient.

v  Potency: how effective is the drug in treatment of various diseases and what effect does it has on patients.

What is Pharmacovigilance?

Pharmacovigilance is also known as ‘drug safety’. It includes assembling, inspection, controlling and interception of adverse effects of drugs & therapies. This is a scientific and process-oriented field in the pharmaceutical world.

It is concerned with every facet of drug development-course, starting from pre-clinical progress to post-market control. This establishes pharmacovigilance as the bottom edge of a life sciences firm.

What is ‘adverse event’?

The ‘adverse event’ for any drugs is the side effect that a drug has on human body. When a drug reacts with the human body and creates a negative effect, then it can lead to serious & dangerous effects on health and a patient might have to go through hospitalization, immobility, permanent impairment or even death in the worse scenario.

It is compulsory for all the clinical trial research auditors to report the adverse effects of the drugs even if there is only a speculation or doubt.

The role of pharmacovigilance is to learn whether the side effects of the drug are within the accepted limit as compared to the usefulness of the drug. In simpler terms, it assesses whether the effectiveness of a drug in treating a disease is worthy enough to let slide some side effects it causes.

Why is Pharmacovigilance so important?

v  It plays a crucial role in drug development. If a company wants to develop, synthesize & commercialize its drugs then it must stick to the rules & regulations. These regulations ask for the efficiency of a drug, its advantages & other benefits for the patients.

v  The main aim of pharmacovigilance is to access drug- and patient safety. Drug safety ensures that the drug does not cause any unwanted and negative effect on the patients during the drug development cycle or when it is ready for sale in the market.

v  Drugs are constantly kept under observation for any side-effects on patients & any new data if generated is organized and handed over to the health authorities at frequent intervals.

 If you are a drug manufacturer/pharma company & looking for pharmacovigilance support, then Turacoz Healthcare Solutions is there to help you.

Turacoz is a medical communication company which provides with end-to-end pharmacovigilance support, from literature monitoring to case processing. It also provides consultancy facilities for pharmacovigilance.

 Turacoz provides the following services related to pharmacovigilance:

v  Construction of entire pharmacovigilance unit

v  Pharmacovigilance voice process support

v  End-to-end case processing

v  Signal disclosure

v  Literature research

v  Reporting of adverse cases

v  Safety report generation

v  Pharmacovigilance Training

Turacoz provides the best of pharmacovigilance support to its clients and extends its full support in all the related activities just to make sure that all the requirements are met efficiently & effectively.

So, if competent Pharmacovigilance support is your concern, reach out to Turacoz Healthcare Solutions for assistance.