Birva possesses more than 20 years of experience in Clinical Quality Assurance. During the past two-plus decades, she's worked in Clinical Research operations around the globe, including the United Kingdom, United States, Japan, Australia, and India to name a few. Birva's knowledge of regulatory requirements also spans the spectrum, with a focus on pharmaceuticals, medical devices and biologics.
With a Master's in Microbiology, Birva brings sponsors deep expertise in Quality Management Systems, Corporate Compliance, Vendor Management, Good Clinical Practices, Corrective Action and Preventive Action, Investigator Site Compliance, Inspection Readiness, Standard Operating Procedure Management and Process Improvement.
