Advanced LC/HR-MS Based Workflow for Extractable and Leachable Analysis
Regulatory agencies such as the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA) have established guidelines and requirements regarding extractables and leachables to ensure the safety and quality of pharmaceuticals products. Compliance with these regulations is essential for obtaining regulatory approval and maintaining market access.
Register now and attend this Webinar to learn:
Latest trends & applications in E&L analysis
Advanced LC/HR-MS based workflows and solutions offered by Agilent
Role of statistical analysis in extractable profiling
Regulatory landscape in E&L analysis
Understanding the quantitation approach
Other webcasts from the series
USP 467 Residual Solvent: Application Updates Tips & Tricks
- Thursday, 06 June 2024, 15:00 IST
Advanced GC/MS | GC/HR-MS Based Workflow for Extractable and Leachable Analysis
- Thursday, 08 August 2024, 15:00 IST
Demystifying USP & ICHQ3D Guidelines for Elemental Impurities
- Thursday, 05 September 2024, 15:00 IST
*Register for all the webinars and get complementary access to The experts guide to Pharmaceutical Impurity Analysis e-book.
Presenter: Dr. Kuldeep Sharma (Sales Development Manager - Pharma, Agilent Technologies)
Kuldeep Sharma has over 19 years of experience in area/s of Bioanalytical research, Drug metabolism & pharmacokinetics and Pharma regulatory compliance. He has accomplished PhD in Biotechnology. His professional journey covers over 12 years in Analytical research (associated with R&D’s of Zydus Cadila, Lambda, Pliva and Jubilant Biosys) and last 7 years in analytical instruments sales, marketing & business development. With over 21 research articles published in international Journals, He presents convention of continues learning.
Presenter: Mr. Praveen Arya (Application Engineer - GC/MS, Agilent Technologies)
Praveen Arya, Application Engineer at Agilent technologies, has a commitment and appreciation for Gas-phase residue applications. In 2005, Mr. Praveen Arya completed his M.Sc. in Food Technology . After post-graduation, he served as a Senior Analyst at SGS, Gurgaon- a commercial testing laboratory for 6 years and developed expertise in Residue analysis using sophisticated chromatographic instruments such as LCMS and GCMS. After that, in 2011, He joined Agilent Technologies as an Application Engineer where he supported country-wide GCMS customers for resolving application issues and method development. He has more than 18 years of experience in residue analysis in food and environmental samples using various high end chromatographic and spectrometric techniques (GC, GCMS, GCMS/MS, TDS, Headspace, Purge & trap etc.). His area of specialization includes new analytical method development and validation as per national and international guidelines.
Presenter: Mr. Ankush Sharma (Regional Marketing Program Manager- APAC (Pharma & Biopharma), Agilent Technologies)
Ankush Sharma is a seasoned professional with over 12 years of extensive experience in sales and marketing across the pharmaceutical and biopharmaceutical sectors. His professional journey commenced with a strong educational foundation, earning a Master's degree in Biotechnology. Building upon this knowledge, he furthered his academic pursuits by obtaining a Master's in Business Administration with a specialization in Sales and Marketing, demonstrating his commitment to blending scientific understanding with strategic business acumen. For the past five years, he has been an integral part of Agilent, serving as the Regional Marketing Program Manager for the India and now Asia-Pacific (APAC) region for Pharma and Biopharma Markets.
