Search Thermo Fisher Scientific
Explore this free series of 5 webinars on pharmaceutical applications and concerns ranging from making implants to API domains and compliance. Click on each of the topics below to learn more.
Register just once for access to the entire series by completing the form at the bottom of this page.
The ever-changing regulatory environment faced by manufacturers in pharmaceuticals and other regulated industries can cause confusion and doubts about compliance. Instrument systems designed to meet regulatory requirements can relieve the burden for manufacturers. How do they do it?
Watch this webinar to see how two different instrument platforms – FTIR and Microvolume UV-Vis – help labs assure compliance in their processes.
During this webinar, you’ll learn:
The Thermo Scientific Nicolet Summit PRO FTIR Spectrometer (for raw and finished material QA/QC) and the Thermo Scientific NanoDrop One Spectrophotometer (for DNA, RNA, and protein quantification) provide confidence when approaching your next audit.
Key Learning Objectives:
Who Should Attend: Lab managers in regulated environments (pharma, biopharma)
Run Time:43 minutes
The distribution of API in a pharmaceutical tablet is a critical factor in developing drugs that are effective when consumed. What’s the best way to figure that out?
The combination of FTIR and Raman spectroscopy with mapping is well-suited for identifying and sizing API domains. Both techniques provide excellent chemical and spatial information about the distribution and concentration of the API in a tablet.
Key Learning Objectives:
Who Should Attend:
Run Time: 1 hour
Reducing costs and improving efficiency have always been a goal, but these needs are increasingly critical for pharmaceutical companies in the current pandemic era. Near-infrared (NIR) spectroscopy is a non-destructive analytical tool that provides solutions from drug development to the QA/QC lab, and in at-line, on-line, or continuous manufacturing processes. Its potential in the pharmaceutical manufacturing value chain is still expanding.
This webinar will highlight NIR’s incredible capabilities across a variety of drug forms, in regulatory compliance, for GMP environments, and more.
Key Learning Objectives:
Who Should Attend:
Run Time: 47 minutes
Injectable implants offer several advantages as drug delivery systems including site-specific release and high patient compliance. Hot melt extrusion (HME) is an ideal method for the manufacture of such implants because it can be scalable from early R&D to commercial manufacturing (often with a single instrument). It can also be done in a continuous manufacturing environment. Watch this webinar for an overview of implant types, materials, and scale-up from development to full-scale manufacturing.
Key Learning Objectives:
Who Should Attend: Scientists and engineers in the pharmaceutical industry who deal with development and production of drugs and medical devices
Run Time:36 minutes
X-Ray diffraction (XRD) offers valuable analytics in pharmaceuticals both for research – providing a crystalline “fingerprint” for impurities, patents, etc. – as well as for quality control in manufacturing – parameter optimization, batch identity, etc. Its non-destructive nature and relatively easy sample preparation benefit all users.
Yet any analysis is dependent on capable sample preparation and the ability to acquire reliable measurements. Add in the regulatory compliance required for pharmaceutical companies, and it means the XRD workflow truly has to function smoothly and consistently to get successful results.
This webinar will show you guidelines not only for sample preparation but also different measurement strategies while complying with even the most recent regulatory requirements.
Key Learning Objectives:
Who Should Attend:
Run Time: 54 minutes
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