Shimadzu_NEWS_201101_Pharma_Special
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The Process

Lead Generation

Preparative LC and LCMS

Lead Generation

Together we are strong

Drug Discovery

From Crude to Powder

Solid-Phase Trapping as a new approach to shorten and improve purification process

Drug Development

Bringing light into darkness

2-D LC and LCMS-IT-TOF – Better drug impurity ID efficiency

Drug Optimization

Future-proof analysis – UHPLC 3.0

<i>Nexera</i> perfectly serves all needs of the Pharmaceutical Industry

Drug Optimization

From powder to pill – quality control of pharmaceutical goods

Active agent analysis using FTIR spectroscopy

Method Development

Method transfer and validation according to Quality by Design requirements

DryLab<sup>®</sup>2010 and <i>Nexera</i> – a powerful combination

Drug Testing

Speed beyond comparison

High speed drug screening and quantification

Drug Testing

Residual Solvents

U.S. Pharmacopoeia – revised General Chapter Monograph <467>

Chemistry/Manufacturing/Control

Extrusion testing made easy

Chemistry/Manufacturing/Control

Big potential with protein based drugs

Quality control of recombinant proteins by N-terminal Edman sequencing

Chemistry/Manufacturing/Control

Analysis of residual catalysts in pharmaceuticals

ICP-OES technology quantifies 14 elements according to EMEA guidelines

Chemistry/Manufacturing/Control

How cleaning validation prevents contamination

Chemistry/Manufacturing/Control

Determination of sodium, potassium and calcium

Analysis of Na, K and Ca with flame atomic absorption spectrometry in microsampling mode

Chemistry/Manufacturing/Control

Quality control of special pharmaceutical organics

Identification with UV spectroscopy

Chemistry/Manufacturing/Control

Quality control of ultra pure water in pharmaceutical manufacturing

Two TOC instruments offering different oxidation methods

Chemistry/Manufacturing/Control

How heavy metals can migrate into pharmaceuticals

EDX series detects elements from C to U – carbon and uranium

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