DRUG SAFETY-PHARMACOVIGILANCE COURSES
Are you passionate about drug monitoring or surveillance and keen about the safety of patients, this career pathway will interest you? Do you have a degree in medicine, pharmacy, or nursing? Well, this career path and plan is perfect for you. At Qtech, we strive to achieve your career goals and make you successful.
DRUG SAFETY
Drug safety is the main aspect of medical therapy that can play a major role in deciding which drug should be given to a patient. Pharmacovigilance (PV or PhV), also known as drug safety, is the pharmacological science relating to the collection, detection, assessment, monitoring, and prevention of adverse effects with pharmaceutical products.
Programs Offered
We offer 4 programs, click below to learn more about each program.
- Drug Safety-Pharmacovigilance Data Management (DSPM) – Package
- Drug Safety Skill-Based-Lessons (DSSB) – Entry
- Drug Safety-Pharmacovigilance Associate(DSAT) – Certificate
- Drug Safety-Pharmacovigilance(ADSA) – Advanced Topics
- Drug Safety-Pharmacovigilance(DSAP) – Role based Projects
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THE ROLE OF DRUG SAFETY PROFESSIONAL
Drug safety associates or assistants work in the medical industry to monitor the safety of medicines and to assess and prevent adverse reactions in patients. A pharmacy safety profession (also known as pharmacovigilance) can include working with clinical research organizations conducting trials, biotechnology companies, pharmaceutical companies, or government agencies such as the National Institutes of Health (NIH). Drug safety assistants need excellent research skills, a solid medical or biological science background, and a deep understanding of the Food and Drug Administration (FDA), European Medicines Agency (EMA) guidelines and regulations. Your responsibilities include analyzing clinical trial data, writing reports, and determining whether a particular drug is safe.
Drug safety assistants need excellent research skills, a solid medical or biological science background, and a deep understanding of the Food and Drug Administration (FDA), European Medicines Agency (EMA) guidelines and regulations. Your responsibilities include analyzing clinical trial data, writing reports, and determining whether a particular drug is safe.
| Job titles you can apply after training | |
|---|---|
| Drug Safety Associate | Drug Safety Assistant |
| Pharmacovigilance Associate | Adverse Event Monitor |
| Medical Case Evaluator | Local Safety Manager (LSM) |
| Drug Safety Manager | Medical Record Extractor |
| Medical Reviewer | Therapeutic Area Lead |
| Global Drug Safety Specialist | Patient Safety Quality Manager |