Author: medipharmsolutions

The activity that is most commonly associated with pharmacovigilance and which consumes a significant amount of resources for regulatory authorities is that of adverse event reporting. Adverse event (AE) reporting... Read More

The Pharmacovigilance course is designed to equip participants with the knowledge and skills necessary to ensure the safety and effectiveness of pharmaceutical products throughout their lifecycle. Through a combination of... Read More

The Pharmacovigilance course is designed to equip participants with the knowledge and skills necessary to ensure the safety and effectiveness of pharmaceutical products throughout their lifecycle. Through a combination of... Read More

Clinical Data Management (CDM) is the handling of information that results from clinical trials. All aspects of processing study information are part of clinical data management. This includes developing and... Read More