Automation in Analytical Laboratories – Purification Solution

Isolation of impurities for further characterization is a routine task in the pharmaceutical industry and is frequently carried out using preparative high‑performance liquid chromatography (HPLC). The small-molecule purification workflow includes method development on an analytical scale, upscaling to preparative conditions, fraction collection, and fraction reanalysis

1. Do you work on compound isolation for further charecterization?
2. Is your system capable of running analytical & Semi prep work automatically?
3. How can you assure highest purity fractions & recveries of compound of your interest?

Presenter: Ms. Paramjeet Khandpur (Product Specialist, Agilent Techologies, India)

Ms. Paramjeet Khandpur, M.Tech. received Bachelor’ degree in Chemical Engineering from VTU University and Master’s under Dr. Parag Gogte in Bioprocess Technology from the Institute of Chemical technology, Mumbai. During her research tenure, she has published 6 research articles in several international journals. Paramjeet is working as Application Scientist in Centre of Excellence Laboratory, Bangalore, Agilent Technologies India Pvt. Ltd. At Agilent, she has been working on liquid chromatography platforms like HPLC, UHPLC, 2D LC and preparative LC solutions. She is working in collaboration with several users in the Pharma/Biopharma industry for method development activities, HPLC to UHPLC method transfer, troubleshooting method related issues and has experience on various workflow of Pharma & Bio-Pharma markets. Prior to joining Agilent, she worked as a faculty at Biotechnology Department, VTU university, Karnataka.