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Laboratory Testing Blog

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An Overview of Skin In Vitro Percutaneous Absorption and Drug Release

Perspectives on Guidelines for Dermal Absorption and Quality of Transdermal Patches

3 Simple Analytical Techniques to Compare Biosimilar mAbs

Meeting Regulatory Requirements for Human Skin Model Integrity Testing

4 Analytical Strategies to Overcome Challenges in Large Molecule Impurities Analysis

A Regulatory Agency Viewpoint on Skin In Vitro Testing Studies

Human Skin Models as In Vitro Testing Methods for Dermal Absorption, Penetration and Toxicology Studies

FDA's 7 Recommendations for Stability Testing of ANDA Products

5 Steps for In Vitro Skin Absorption and Drug Release Method Validation

4 Key Steps to Characterize and Qualify Unknown Trace Impurities

Isolation and Characterization of Trace Impurities in Pharmaceutical Products

Conducting Quantitative Oligonucleotide Chemical Analysis

Unique Analytical Method Challenges for Polysulfated Carbohydrates

3 Tips to Overcome Challenges in Analyzing Peptides and Proteins by LC-MS/MS

Developing Analytical Test Methods For the Simultaneous Quantitation of Actives, Preservatives & Impurities

Chromatographic Method Analysis for Oligonucleotides Using UPLC and UPLC-MS/MS Detection

Injectable Polymeric Particulate System In Vitro Testing Challenges

What is Good Laboratory Practice (GLP)?

Method Development Challenges for Analysis of Aggregation in Protein Mixtures

Overcoming Challenges in Protein Molecule Analysis

Testing the Freshness of Marine Oils

Analytical Techniques for Determining Free Fatty Acids in Plasma

The Impact of OECD Guidelines on Skin Absorption Studies

New 5 Page Whitepaper: Impact of Proposed Changes to USP 231 Heavy Metals Testing

Alternative Approaches For Skin Integrity Testing

Method Development Challenges in the Bioanalysis of Biotherapeutics

An Optimized Analytical Methodology for Monoclonal Antibodies (mAb) Testing

Alternative Analytical Techniques for the Separation and Detection of Jasmonic Acid

Review of Proposed USP Changes to Heavy Metals Testing

Analytical Testing Approaches for Phytohormones, Fatty Acids, Carbon and Nitrogen Metabolites in Plants

Proposed Changes to USP Heavy Metals Analytical Testing

Top 10 Stability Storage and Testing FAQ's

Top 5 Laboratory Testing Blog Articles in 2011

Using CE, HPLC and UPLC for Peptide Drug Product Characterization

New 11 Page Whitepaper: Predicting Nasal Drug Absorption With In Vitro Release Testing

Reproducibility of In Vitro Release Rate Testing in Human Skin Models

Measuring Reproducibility in an In Vitro Release Rate Testing Method

New Analytical Method Approaches for Enzyme Characterization

EMA Issues New Guideline on Bioanalytical Method Validation

Creating Mass Balance Studies for In Vitro Release Testing

Pharma Industry Gathers Together To Talk Outsourcing

Analytical Methods Used to Determine Disulfide Bond Linkage Patterns

General Analytical Approaches for Full Glycoprotein Characterization

A New Model For Pharmaceutical Drug Development?

Characterization, Separation & Quantitative Analysis of Glycopeptides in Monoclonal Antibodies

New Whitepaper: Challenges with Quantitative Bioanalysis of Proteins and Peptides

A General Approach for Quantitative Bioanalysis of Peptides and Proteins by LC-MS/MS

Importance of Glycoprotein Characterization in Biopharmaceuticals

The Importance of Mass Spectrometry for Bioactive Peptides

Quantitative Analysis with Mass Spectrometric Detection No Longer Limited to Small Molecules

A New Laboratory Research and Testing Group on LinkedIn

Thesis Chemistry Launches Green Chemicals Initiative

4 Different Testing Approaches For the Detection of Heparin

Analytical Approaches For Determining Disulfide Bonds in Proteins

7 Different Approaches for DNA Testing and Analysis

Modernizing Drug Quality Testing

Learn In Vitro Release Testing Best Practices [eBook]

Peptide Mapping - An Essential Analytical Development Technique

7 Quality Considerations for Large Molecule Product Development

4 Approaches for In Vitro Release Testing of Intraocular Implants

Why Biopharmaceuticals?

Dissolution Apparatus Basket and Paddle Wobble Testing

Analytical Techniques for the Quantitative Detection of Glycoproteins

In Vitro Testing Considerations for Nasal Drug Delivery

In Vitro Testing for the Development of Semisolids Using Human Skin Models

Assessing Human Cadaver Skin Models for In Vitro Testing

Different Approaches for Analysis of N- and C-Terminal Peptides

3 Additional In Vitro Testing Considerations for Topical Steroids

Antimatter: A Major Scientific Breakthrough?

EMA Considering New Guidance for Tech Transfer Test Method Validation

AAPS 2010 Annual Meeting Thoughts

5 Biggest Diteba Changes in the Past 5 Years

Stability Storage Considerations for Soft Gelatin Capsules

Promising Approaches for Determining Protein-Ligand Binding Constants

Alternative Approaches for Determining Protein-Ligand Binding Constants

Approaches to Determining Protein-Ligand Binding Constants

In Vitro Testing Models for Nasal Drug Delivery

Qualitative and Quantitative Aspects of Peptide Mapping Using UPLC-UV

Peptide Mapping Using UPLC-UV Method Development Techniques

USP Advisory Panel Re-issues Draft USP General Chapters on Topical & Transdermal Drug Products Dissolution Testing into PF 35(3)

Dissolution Testing Methods for Poorly Soluble Compounds - continued

Developing Dissolution Testing Methods for Poorly Soluble Compounds

Adapting New Analytical Method Technologies with Scientific Expertise

UPLC Throughput Improvements Offer Much Faster Turnaround Times

R&D Intensive Solutions for the Pharmaceutical Industry

Features of In Vitro Testing for Topical Semisolids

Utilizing Capillary Electrophoresis (CE) in Pharmaceutical Analysis

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