Raw Material Identification in Pharmaceutical Application
Growth of domestic pharma and recent industry trends – Spotlight on Revised Schedule M
Raw material identification (RMID) is a regulatory-enforced step in drug manufacturing for pharmaceutical and biopharmaceutical organizations. With the new updates made to Schedule-M, laboratories will see an increase in ID testing performed in manufacturing sites across India.
While a critical step in ensuring quality and safety, conventional approaches create unnecessary waste, including:
- Misallocation of resources – conventional approaches cause logistical bottlenecks and inundate highly trained scientists with tedious work- delaying the release to production.
- Environmental waste – physical sampling of raw materials causes unnecessary environmental waste, creating challenges in reaching sustainability goals.
- Economic waste – conventional approaches require resource-intensive processes to move raw materials from receipt to production.
Taking a new approach to Raw Material ID with Spatially Offset Raman Spectroscopy (SORS) provides zero-waste workflows from an economic and environmental perspective. Handheld SORS enables non-invasive verification through opaque and transparent containers. This approach eliminates waste from conventional sampling and boosts sustainability in drug manufacturing. This webinar will review how Agilent helps individuals reach their efficiency, quality, and sustainability goals simultaneously.
What you will learn:
- Learn how the Vaya SORS technology and usability enable rapid RMID by basic operators in the warehouse for the fastest release to production.
- Explore how the Vaya Raman achieves zero-waste workflows in RMID, helping reach sustainability goals without compromising data quality or efficiency.
- Understand the holistic and long-term benefits of choosing true through-barrier verification for one’s RMID.
Who should attend:
- QC lab managers, analysts, and scientists
- PAT Scientists
- Manufacturing managers and warehouse managers
- Process development managers
- VP of quality and/or operations
Presenter: Frederic Prulliere (Product Manager Raman ID, Agilent Technologies)
Frederic Prulliere, is the Product Manager for the Raman-ID product line at Agilent Technologies. Frederic has been working in the Analytical Instrumentation Industry for over 10 years focusing on Raman, NIR and FTIR mobile solutions.Based in the US, Frederic now leads the product development of Spatially Offset Raman Spectroscopy based solutions, in particular for the verification of raw materials at reception.
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.
