Ask the Experts: Ensuring the quality of raw materials and active pharmaceutical ingredients (API) is a critical step in the drug manufacturing process with impacts on speed and cost of production, product and patient safety, and, ultimately, your brand reputation.
Join our panel of experts to discuss analytical techniques that can help support your work in drug discovery. We offer a complete range of spectroscopy and software solutions, including FTIR, Raman, and UV-Vis, with applications that can facilitate the process of identifying and validating therapeutic targets to move forward as a potential drug candidate.
Handheld Raman spectrometers have fundamentally changed how the pharmaceutical industry performs incoming raw material identification.
Micro volume measurements take place at very small pathlengths, typically ≤ 1 mm. Reducing the pathlength has the same effect as diluting the sample for measurement in a conventional instrument. This allows you to save on the sample amount used for UV/VIS spectrophotometry.
Subvisible particulate testing is critical to assess the safety of medical devices, and particulate contamination should be minimized to avoid possible negative health consequences to the patient.