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Evolving Analytical Workflows & Regulatory Compliance in Pharmaceuticals

RECORD | Already taken place Fr, 18.7.2025
Explore method modernization, impurity analysis, and data integrity in pharma. Gain expert insights from leading scientists in this PharmaFrontiers webinar.
Go to the webinar
Agilent Technologies: Pharma Frontiers Live Webinar Series: Analytical Techniques, Advances in Chromatography and Regulatory Compliance
Agilent Technologies: Pharma Frontiers Live Webinar Series: Analytical Techniques, Advances in Chromatography and Regulatory Compliance

Join us for an enlightening webinar series designed to empower academicians and researchers by exploring the latest advancements and opportunities in pharmaceutical sciences. At Agilent, we recognize the unique challenges faced by academicians, researchers, and students. At PharmaFrontiers, we have curated a series of content tailored to address your needs and unlock new opportunities.

The PharmaFrontiers seminar series is designed to provide you with valuable knowledge, insights, and practical skills.

Topics to be covered:

  • Understanding Method Modernization - USP<621.
  • Monitoring & Control of Impurities in Pharmaceuticals: Analytical Techniques and Regulatory Compliance.
  • From Lab to Market: The Crucial Role of Data Integrity in Pharma.

Presenter: Dr. Kailash Asati (Head Analytical Research, Zydus Research Centre, Zydus Lifesciences Ltd, Ahmedabad, India)

Dr. Kailash by education, holds a PhD degree in Organic Chemistry from Sagar University and an MBA in operations from Sikkim-Manipal University, India. He has many publications in scientific journals.

Dr. Kailash, by professionally serving the pharmaceutical analytical domain (Generic and Discovery) for the last two and a half decades. He has experience and expertise in different verticals in the discovery and development of pharmaceutical industry at various capacities technical expert, in management and leadership role.

His expertise is on Analytical Sciences of Development and advance techniques, projects management, Quality & Compliance, Health authority audits, Technology transfer, Operation excellence and GLP/GMP analytical facility setup for small molecules.

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

Kuldeep Sharma has over 19 years of experience in the areas of bioanalytical research, drug metabolism & pharmacokinetics, and pharma regulatory compliance. He has accomplished a PhD in biotechnology. His professional journey covers over 12 years in analytical research (associated with R&D at Zydus Cadila, Lambda, Pliva, and Jubilant Biosys) and the last 7 years in analytical instrument sales, marketing, and business development. With over 21 research articles published in international journals, he presents the convention of continuous learning.

Presenter: Mr. Sridhar Atmakuri (Sales Development Manager - Compliance Specialist, Agilent Technologies)

Sridhar Atmakuri is a Master of Pharmacy graduate from Andhra University, Visakhapatnam, India. He has worked with the top pharma MNCs like Ranbaxy (now Sun Pharma), Dr. Reddy’s Labs, and analytical solution providers. He has a rich experience of 17 years in areas and disciplines of Pharma Research, Chromatography, Mass Spectrometry, Quality, Compliance, Data Integrity and Validations. He is an APIC Certified ICH Q7 GMP auditor and ISO 9001:2015 QMS Lead Auditor and has also trained many people on different topics of pharma quality and compliance.

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