Pharmacovigilance

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Pharmacovigilance (PV) is an important part of the healthcare system because it

assesses, monitors, and discovers drug interactions and their effects on humans.

Pharmaceutical and biotechnological medicines are intended to cure, prevent, or

treat diseases; however, there are risks, particularly adverse drug reactions (ADRs),

which can be fatal to patients. Thus, for medication safety, ADRs monitoring is

required for each medicine throughout its life cycle, including pre-marketing, early

stages of drug design, clinical trials, and post-marketing surveillance. PV is

concerned with the detection, evaluation, comprehension, and prevention of ADRs.

Furthermore, PV has a long history of mining spontaneous reports submitted to

national surveillance systems.

MEPharma provides comprehensive Pharmacovigilance and safety monitoring

services ranging from early development assistance to post-approval initiatives. We

have experienced and skilled medical professionals on staff who are well-versed in

regulatory requirements.