Modernize your Analytical Methods to enhance Lab Productivity: USP 621 Decoded

The Chromatography chapter, USP<621> Stage - 4 Harmonization, was published on November 19, 2021, and officially implemented on December 01, 2022. The chapter was formally approved by the General Chapters–Chemical Analysis Expert Committee in accordance with the Rules and Procedures of the Council of Experts (Nov 2021). With USP<621> Chapter becoming official, Chromatography scientist have gained flexibility to explore Superficially porous particles and faster isocratic/ gradient methods for USP monographs.

Revised USP <621> introduces allowance for a shift from entirely porous silica-based analytical columns to superficially porous particles. Also, with recommendations permitting adjustments in both isocratic and gradient compendial methods, industries adhering to these guidelines can now explore an opportunity to improve their old HPLC methods to align better with their organizational objectives.

These goals include faster methods for quicker product release, reduced extra work for method revalidation, reduced solvent consumption for a better and safer lab environment, and reduced cost per sample.

Join us to discover:

1. Strategies for optimizing chromatographic performance using right HPLC system.
2. Innovative column technology for enhanced performance and time efficiency.
3. Methods to enhance sustainability by minimizing solvent usage.
4. Adjustments achievable without the need for revalidation, including new permissible GRADIENT method changes.
5. Techniques for enhancing laboratory productivity and reducing operational costs.

Presenter: Sunil B Lakhmapure (Technical Support Specialist, Agilent Technologies India)

Sunil holds 19 year plus experience in the analytical field with major exposure to LC/GC with Single Quad, Triple Quad and high resolution (QToF) mass spectroscopy. Started career in Pharma R&D as a scientist with hands on experience on high end instruments like LC/MS, XRD & NMR. Developed & published application notes using Chromatographic techniques on real world samples/issues at various levels.

Dr. Kuldeep Sharma (Sales Development Manager - Pharma, Agilent Technologies India)

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.