![]() Other medical cases including hospitalization, significant disability, congenital anomaly or other medically important events require this process to be completed in 2-7 days. In a life-threatening case, or in the case of death, DSAs are given 1-2 business days to process the necessary information and pass it onto other teams. As soon as an alert of a serious adverse event (SAE) is raised the clock starts and sets into motion the necessary tasks that need to be completed to process the events. Once a drug has been marketed the work for a DSA begins after. Ensuring work is well distributed among each member of the team and is training compliant. Participants in the class should also have some medical knowledge as the course will go into detail about specific medical concepts. Being a significant part of the pharmacovigilance and safety services (PVSS) department, a Drug Safety Associate (DSA) is a key job profile for drug safety management in clinical trials and post marketing surveillance (PMS). Well versed with ATC coding following the latest ATC guidelines. MedDRA Coding This class is directed to individuals who already have some familiarity with MedDRA but desire more in-depth training on how to properly code using MedDRA. This program provides an in-depth understanding as presentations for Medical Coding and Practices followed using MEDdra Software for capture, entry and reporting of various Adverse Events per therapeutic areas, followed by Pharmaceuticals for Drug safety and Pharmacovigilance Reporting and monitoring process. Qtech-Sol is a Clinical Science Training Provider.
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