Technical Papers

265 Results

Elemental Impurities Regulations View from a CRO

Elemental Impurities Regulations View from a CRO

RSSL | 02-Nov-2016 | Technical / White Paper

Regulatory control of elemental impurities in pharmaceutical products has long been discussed, with both the European Pharmacopeia (EP) and the United...

The Time for Supply Chain Transformation Has Come

The Time for Supply Chain Transformation Has Come

Catalent Pharma Solutions | 26-Sep-2016 | Insight Guide

Adaptive protocol designs, shrinking trial sizes and a growing focus on patients are just a few of the clinical trial trends and recent innovations that...

Excellence in Pharmaceutical Analysis

Excellence in Pharmaceutical Analysis

Butterworth | 16-Sep-2016 | Data Sheet

Butterworth specialise in Quality Control Analysis, Method Development, Validation & Stability Testing of Raw Materials, API, Finished Product and...

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Building the Future: Using Simulation Effectively

Baxter BioPharma Solutions | 09-May-2016 | Case Study

This case study provides an in-depth look at Baxter BioPharma Solutions’ latest expansion at their Halle, Germany cytotoxic facility, offering insight...

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Respiratory Patient Clinical Trials

SGS Life Science Services | 25-Apr-2016 | Technical / White Paper

This white paper will examine the use of sputum induction as a pharmacodynamic method to optimize respiratory patient clinical trials, including comparison...

Data Mining At The FDA

Data Mining At The FDA

Oracle Health Sciences | 20-Apr-2016 | Technical / White Paper

The FDA has recommended the use of data mining to the drug industry, and their new Data Mining at FDA white paper summarizes their past and current data...

What do you need to know about Direct-To-Patient

What do you need to know about Direct-To-Patient

World Courier | 18-Apr-2016 | Technical / White Paper

In the world of clinical trials, one of the greatest challenges to overcome is the recruitment and retention of qualified patients. Finding patients who...

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