Divya Regulagedda
Manager (Global SME)
Divya Regulagedda is analytical person from technical perspective and have experience in the field of E & L for 11+ years. She has hands on experience with LC-MS/MS, LC-QTOF, GC-MS/MS, ICP-MS and IC.
Previously, she worked with a CRO and was responsible for the work of E &L.
Currently, she is responsible for the E & L work in Insud Pharma for Pharmaceutical products and medical devices.
Also, she has experience with risk assessments and toxicological evaluations.
DAY 1: February 27th, 2025
SESSION: How to implement effective E&L study designs
◆ Sample preparation, extraction studies and quantification.
◆ Classifying and identifying targeted substances.
◆ Risk assessment and profiling for extractables.
◆ Assessment of stability studies and leachables.
DAY 2: March 8th, 2024
SESSION: E&L testing for medical devices
◆ Chemical characterisation of medical device materials and ISO 10993-18.
◆ Evaluation of biocompatibility and toxicological risk.
◆ The verification of analytical methods.
