Sushma Ejanthkar

I am passionate about patient safety and regulatory compliance in pharmaceutical industry. With over 2 years in pharmacovigilance and 4 years in regulatory. I have expertise in drug safety , regulatory reporting and project management.

I've gained a strong understanding of monitoring and reporting adverse drug reactions in my pharmacovigilance career. I'm skilled in data analysis, report preparation, and meeting regulatory requirements. I also manage drug safety projects effectively.

Key Skills

Drug Safety

Regulatory Reporting

Risk Management

Data Analysis

Project Management

Team Collaboration

I'm eager to keep learning and growing professionally. Let's connect to explore how we can work together to improve patient safety and healthcare.

I have done Masters in Pharmaceutical Sciences in Greenwich University London