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From Routine to Remarkable LC Analysis: Transforming Productivity with USP 621 Modernization

ZÁZNAM | Proběhlo Čt, 8.1.2026
Zúčastněte se tohoto technického webináře, abyste se seznámili s nejnovějšími povolenými změnami v USP <621> a zjistili, jak mohou proměnit ekosystém vaší LC laboratoře.
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Agilent Technologies: From Routine to Remarkable LC Analysis: Transforming Productivity with USP 621 Modernization
Agilent Technologies: From Routine to Remarkable LC Analysis: Transforming Productivity with USP 621 Modernization

Stay Ahead with the Latest USP <621> Guidelines

Are you ready to make your lab more productive, compliant, and sustainable?

Join this technical webinar to explore the latest permissible changes in USP <621> and learn how they can transform your LC lab ecosystem.

Key important questions to be addressed:

  • Have you adopted the latest permissible changes provided in USP <621> for the HPLC method?
  • Do you know how USP <621> permissible changes your LC Lab ecosystem to peak productivity?
  • Do you want to reduce your run times 2X to 5X without compromising compliance needs?
  • Does your organization want to bring a change to meet sustainability criteria?

Who Should Attend?

  • Pharma Analytical & Quality professionals
  • HPLC scientists aiming for peak productivity
  • Department heads and QA leaders working with USP or similar pharmacopeia methods

Don’t miss this opportunity to stay ahead of the curve and outperform the competition.

Presenter: Dr. Kuldeep Sharma (Business Development Manager - Pharma, Agilent Technologies)

Dr. Kuldeep Sharma has over 23 years of experience in area of pharmaceuticals analytical R&D, analytical method development & validation, clinical & pre-clinical studies and regulatory compliance. With a Doctorate of Philosophy in Biotechnology, His professional journey covers a true blend of Technical and Commercial industry insight with over 13 years as Analytical Research Scientist (with leading Pharma companiese.g. Zydus Cadila, Lambda, Teva and Jubilant Biosys) and recent10 years as techno-commercial expert leading Analytical instruments sales strategies and marketing initiatives.

During his industry experience, he had accomplished leading roles in domains covering conduct of Analytical research, Pharma quality compliance, Pre-Clinical and analytical studies. With over 21 research articles published in international Journals and 5 technical write-ups in leading magazines; He presents convention ofcontinues learning enabling him acquire advance certifications of Lean Six Sigma-Black Belt and MBA (Operations Management) in continuation to his professional journey.

Presently he is associated with AGILENT Technologies as Sales Development Manager- Pharmaceuticals Markets (India).

Presenter: Ms. Sreelakshmy Menon (Application Scientist, Agilent Technologies)

Sreelakshmy is working as an Application Specialist, at Agilent Technologies for the past 11 years. She has experience in working with Analytical techniques such as HPLC, UHPLC, CE, SFC, Method development solutions etc. Her primary interest is in developing liquid chromatography application solutions focusing on AQbD approach concentrating on pharma and biopharma workflows. To her credit she holds around12 publications on innovative Liquid Chromatographic solutions.

Agilent Technologies
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