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Analytical validation of accelerator mass spectrometry for pharmaceutical development
The validation parameters for pharmaceutical analyses were examined for the accelerator mass spectrometry measurement of 14C/C ratio, independent of chemical separation procedures. The isotope ratio measurement was specific (owing to the 14C ...
Paul Gabbott and Tim Mann PETA Solutions Chalfont Road, Seer Green, Beaconsfield, Buckinghamshire HP9 2FX
Thermogravimetric Analysis (TGA) of materials is commonly used to provide information on the weight loss as a sample is heated or held isothermally. Pharmaceutical materials often show weight losses associated with the loss of solvent/ water, desolvation or decomposition of the sample. This ...
Changes to heavy metals test procedures for the analysis of pharmaceuticals and dietary supplements are under review with new standards set to be in place by mid-2013.1 The intention of this review is to update current analytical testing historically performed using United States Pharmacopeia (USP) <231>. The revisions (USP<232>, USP<233>, and USP<2232>) are designed to set safer limits for ...
Topical Dermatological Formulation Development “Things You Should Know”
Formulation Development of Topicals is Different Pg 1 Developing a Target Product Profile is Important Pg 2 How to Select the Topical Dosage Form Pg 3 Definition of a “Successful” Formulation Pg 4 The Need for Multiple Excipients Pg 5 The Formulation Development Process Pgs 6-7 Challenging Analytical Method Development Pg 8 ...
Paul Gabbott and Tim Mann PETA Solutions Chalfont Road, Seer Green, Beaconsfield, Buckinghamshire HP9 2FX
Thermogravimetric Analysis (TGA) of materials is commonly used to provide information on the weight loss as a sample is heated or held isothermally. Pharmaceutical materials often show weight losses associated with the loss of solvent/ water, desolvation or decomposition of the sample. This ...
Case Study: International Pharmaceutical Company
The client is an international pharmaceutical company operating in 143 countries around the world with over 40,000 employees worldwide.
The primary challenge for the client was to create a workflow that enabled their sales group to process contracts and get the necessary approvals and reviews. It was important to implement a thorough approval ...
Automated analysis improve accuracy and robustness exemplifying QbD. Examine various issues with methods that will help you better understand the potential of QbD in the pharmaceutical industry and how they can improve assay results.
Cleaning validation is essential in order to prevent contamination and cross contamination of pharmaceutical products. Introduced here is the determination of the quantitation limit for the Shimadzu UV-1800 spectrophotometer by absorption photometry, with samples consisting of detergent A used for cleaning in the pharmaceutical field, and the typically used pharmaceutical materials ...
A brief discussion about dissolution is important to understand the relevance of automation to this eld. Dissolution testing is a critical test for measuring the performance of a drug product. In the last few years, the importance of the dissolution test has increased substantially. Dissolution testing plays several key roles in the pharmaceutical industry. Primarily, the test is a quality ...
Market Drivers: RFID In The Pharmaceutical Supply Chain 6
HF/UHF Primer – Physics And Technology Characteristics 10
HF/UHF Technology Deployment Considerations 15
Report From The Field – HF Item-Level Pilots 18
Item-Level Visibility in the Pharmaceutical Supply Chain – A Comparison of HF and UHF RFID Technologies 3
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