Regulatory Affairs Specialist
2
Resources
46
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Dr. Emily Watson specializes in FDA and EMA regulatory submissions.
10+ years of experience
2 resources by Dr. Emily Watson
Master the principles and practices of obtaining ethically valid informed consent in clinical research.
Master the critical requirements for identifying, documenting, and reporting adverse events to ensure participant safety.
Regulatory Affairs Specialist
2
Resources
46
Total Views
0
Downloads
N/A
Avg Rating
Dr. Emily Watson specializes in FDA and EMA regulatory submissions.
10+ years of experience
2 resources by Dr. Emily Watson
Master the principles and practices of obtaining ethically valid informed consent in clinical research.
Master the critical requirements for identifying, documenting, and reporting adverse events to ensure participant safety.