Shwetha Madhur

Shwetha Madhur started working at Granzer Regulatory services as Regulatory consultant from June 2019. She finished her Bachelor of Engineering in Biotechnology from India and started working as a research associate in a small start up which focuses on bioinformatics (Shodhaka).

After that she worked as a regulatory associate at Liquent Inc. (A Paraxel company), where she handled publishing for many US and EU submissions.

After Paraxel she worked for PharmaLex in regulatory operations department for several years. She successfully handled different regulatory operations projects for different clients including XEVMPD. She has expertise with different electronic submission publishing softwares. She is also very well versed with post authorization submissions for EU and US.

 

Key knowledge areas:

• Electronic submissions & lifecycle management
• Post-authorization activities