Technical Papers

674 Results

Achieving PAT Goals with Process Analytics Equipment

Achieving PAT Goals with Process Analytics Equipment

Mettler Toledo International Inc. | 22-Feb-2010 | Technical / White Paper

“The main emphasis of PAT is on understanding and controlling the process, and not trying to find exotic technologies for doing so.”(Ajaz Hussain, former...

The urgent need for qualified transport providers

The urgent need for qualified transport providers

World Courier | 25-Jan-2010 | Technical / White Paper

In light of sobering statistics from the MHRA, WHO and others about the quality of temperature-controlled drugs and medicinal products arriving at global...

Optimizing capsule counting accuracy

Optimizing capsule counting accuracy

Mettler Toledo International Inc. | 20-Jan-2010 | Case Study

METTLER TOLEDO was approached by a leading gelatin capsule manufacturer to optimize their capsule counting system. For this new capsule bag filling project...

Automated determination of active-substance content

Automated determination of active-substance content

Metrohm – customized analysis for the pharmaceutical industry | 27-Oct-2009 | Application Note

Active ingredients in pharmaceutical tablets can only be determined after several sample preparation steps. Automation with Metrohm’s 815 Robotic Soliprep...

Why, When and How to Conduct Human 14C ADME Studies

Why, When and How to Conduct Human 14C ADME Studies

SGS Life Science Services | 23-Oct-2009 | Technical / White Paper

Learn about the strategies for managing the risk related to drug metabolites, and how the final 14C-human ADME studies should be conducted; includes: 3...

Understanding The 505(b)(2) Approval Pathway

Understanding The 505(b)(2) Approval Pathway

Camargo Pharmaceutical Services | 21-Oct-2009 | Data Sheet

Discover how Camargo Pharmaceutical Services’ expertise in the 505(b)(2) approval pathway can teach old dogs new tricks. In this Q&A, Ken Phelps discusses...

White Paper on USP <467> Residual Solvents

White Paper on USP <467> Residual Solvents

SGS Life Science Services | 25-Sep-2009 | Technical / White Paper

The current USP <467> went into effect over one year ago. Need assistance with USP <467> Implementation? Let SGS Life Science Services update...

Handling Protocols Key Consideration in HPAPI Market

Handling Protocols Key Consideration in HPAPI Market

SAFC Pharma | 18-Sep-2009 | Technical / White Paper

Over the past 10 years, the manufacture of highly potent active pharmaceutical ingredients (HPAPIs) has become increasingly attractive to contract manufacturers...

Automated determination of active-substance content

Automated determination of active-substance content

Metrohm – customized analysis for the pharmaceutical industry | 01-Sep-2009 | Application Note

Active ingredients in pharmaceutical tablets can only be determined after several sample preparation steps.Automation with Metrohm’s 815 Robotic Soliprep...

White Paper on Extractables and Leachables Testing

White Paper on Extractables and Leachables Testing

SGS Life Science Services | 28-Aug-2009 | Technical / White Paper

Need help with Extractables and Leachables Testing? Trust SGS Life Science Services to help your organization stay current with regulations. Download and...

How Automation Can Contribute to Quality by Design Initiatives.

Quality By Design: The Automated Pharmaceutical Assay

Sotax - Solutions for Pharmaceutical Testing | 25-Aug-2009 | Application Note

This paper provides a very brief overview of Quality by Design in the Pharmaceutical Industry focusing down to the pharmaceutical assay. Example flow charts...

Combinatorial Pharmacology in Mice

Combinatorial Pharmacology in Mice

BASi | 20-Aug-2009 | Technical / White Paper

Innovative In Vivo Sampling InstrumentationSet up your lab from start to finish! The comprehensive BASi Microdialysis System (BMS) includes everything...

PEG Purity for API Stability

PEG Purity for API Stability

Croda Health Care | 10-Jul-2009 | Technical / White Paper

One of the main challenges in the pharmaceutical industry is the ability to produce stable drug formulations, and excipient purity is now believed to have...

Publish your Technical Paper on this Website

Publish your Technical Paper on this Website

William Reed Business Media: Publish your Technical Paper on this Website | 09-Jun-2009

Promote your company’s technical expertise towards decision makersPublish your Technical Paper on this website.Benefits:· 71% of industry professionals...

Unmasking the Blind of Over-Encapsulation.

Unmasking the Blind of Over-Encapsulation.

Almac Group | 01-Jun-2009 | Technical / White Paper

Over-encapsulation of comparator products is now a widely accepted procedure used throughout the clinical supplies industry. While the process itself may...

Improve Life Sciences Manufacturing Compliance

Improve Life Sciences Manufacturing Compliance

Aegis Analyticals | 28-Apr-2009 | Technical / White Paper

Improve Life Sciences Manufacturing Compliance In today’s life science manufacturing environments, compliance has taken on new meaning. This paper explores...

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