Printing Inks
Sensient Pharmaceutical Technologies  Sensient Technologies is the world's leading supplier of flavors, fragrances and colors used to make a diverse variety of foods and beverages, pharmaceuticals, cosmetics, home and personal care products, specialty...
Colorcon  Colorcon is a world leader in the development, supply and technical support of formulated coatings and other excipients for the pharmaceutical industry. Our best-in-class products and pharmaceutical technologies are...
Morgan Direct Inc.  Morgan was founded in 2000 with a faith base initiative.Its mission is to help clients succeed through unparalleled prospect marketing solution that deliver only the highest rate of investment. It has worked with...
UVP LLC  UVP, LLC is the global leader in life science imaging supplying BioImaging Systems for academic, biopharmaceutical and biotechnology applications.
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Printing Inks Research Library

Assessment of Veriteq viewLinc Environmental Monitoring System Compliance to 21 CFR Part 11Requirements
Veriteq, a Vaisala company 		The 21 CFR Part 11 rule states that the FDA view is that the risks of falsification, misinterpretation, and change (without leaving evidence) within the GMP environment are higher with electronic records than paper records, and therefore specific controls are required. The Veriteq validatable data logging system is a “hybrid” system that employs the use of both electronic records and signed ...
 
Time to Act Serialization White Paper
PRISYM ID Limited 		Time to Act - Has Judgment Day Arrived for Counterfeit Drugs? An Introduction to the Challenges Presented by Product Codification & Serialization in the Pharmaceutical Sector Introduction It is well recognized that the counterfeiting of pharmaceutical drugs and medical devices is a real and constant threat to patient safety. It is a global issue that affects all of us. It doesn't recognize ...
 
Assessment of Veriteq vLog Validation System Compliance to 21 CFR Part 11Requirements
Veriteq, a Vaisala company 		The 21 CFR Part 11 rule states that the FDA view is that the risks of falsification, misinterpretation, and change (without leaving evidence) within the GMP environment are higher with electronic records than paper records, and therefore specific controls are required. The Veriteq validatable data logging system is a “hybrid” system that employs the use of both electronic records and signed ...
 
Using Proteome Profiler antibody macroarrays to assess kinase phosphorylation and activation
R&D Systems, Inc. 		Antibody arrays are solid matrix assays designed to simultaneously monitor changes in the expression or post-translational modication of multiple cellular protein targets. The multiplexing capabilities are possible due to the “printing” of individual antibodies at precise and dened positions (or coordinates) on the matrix. These arrays offer a rapid and economical way to identify kinase pathways ...
 
Qualitative and Quantitative Aspects of Peptide Mapping Using UPLC-UV
Diteba Research Laboratories Inc. 		Qualitative and Quantitative Aspects of Peptide Mapping Using UPLC-UV Peptide mapping or peptide finger printing produced is characteristic for a particular protein and the UPLC technique can be used to separate a mixture of peptides. Normally, recombinant proteins are developed for therapeutic purposes. Peptide mapping is used to confirm the primary structure of a protein, identify ...
 

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