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    Chromatography ForumAnalytical Training Solutions日本語
  • Home/
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Pharmaceutical

Explore the intricacies of separation science within the pharmaceutical industry. Unveil techniques and technologies vital for isolating, purifying, and analyzing compounds, fostering advancements in drug development, quality control, and research. Discover the latest innovations driving precision and efficiency in pharmaceutical separation processes.

Illustration of RNA strands representing oligonucleotide structures
Articles

LC/MS Impurity Profiling for Oligonucleotides

ByAimee Cichocki
Scientist reviewing analytical data for 21 CFR Part 11 compliance
Articles

Data Integrity in LC/MS: What 21 CFR Part 11 Means for Pharma QC Labs

ByAimee Cichocki
Video thumbnail
Video

Biologics QC: Managing Variability with LC, MS, and Light Scattering

ByAimee Cichocki
Abstract image representing speed in LC/MS automation
Articles

Why LC/MS Automation Matters Beyond Speed

ByAimee Cichocki
3D representation of oligonucleotides in a solution
Articles

When Does Low-Flow LC/MS Make Sense for Oligonucleotide Analysis?

ByAimee Cichocki
Scientist adjusting gas chromatography equipment for alternative carrier gases
Articles

Navigating the Helium Shortage: Transitioning to Alternative Carrier Gases in GC

ByShiama Thiageswaran
Scientist demonstrating Biotage PrepXpert 8 with a gloved hand pointing to screen.
Webinars

Advances in Antibiotic Extraction from Water: An Automated SPE Approach

ByBiotage
Available on Demand
Visual representation of compound semiconductor fabrication with layered designs.
Articles

Why Separation Science is the New Gatekeeper of Semiconductor R&D

ByShiama Thiageswaran
Healthcare professional demonstrating LC/MS data lifecycle
Articles

From Raw Data to Report: Protecting the LC/MS Data Lifecycle

ByAimee Cichocki
wastewater analysis and high-resolution mass spectrometry
Articles

The Evolving Landscape of Wastewater Analysis: From High-Res Screening to the Nanoplastic Frontier

ByShiama Thiageswaran
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Pharmaceutical - Topics
  • Impurity Analysis
  • QbD & Method Development
  • DMPK & ADME-Tox
  • Pharmaceutical Regulations
  • Extractables & Leachables
  • Process Analytical Technology & Continuous Manufacturing
  • Quality Assurance & Quality Control
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