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.
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.
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