All aspects of the pharmaceutical industry are subject to stringent regulations, from clinical trials through to drug packaging. In fact, blister …[Read more...]about Pharmaceutical Packaging Testing for Suitability
Read and download white papers on analytical chemistry topics from Jordi Labs' chemists.
Mitigating Uncertainty Factors in E&L Testing
Extractables and leachables (E&L) testing is a critical part of ensuring product quality in a wide range of application areas, specifically those …[Read more...]about Mitigating Uncertainty Factors in E&L Testing
ISO 10993-18 Expands to Account for Variability
In the past 15 years, ISO 10993-18 has become a guiding light for professionals at every stage in the medical device manufacturing and supply chain, …[Read more...]about ISO 10993-18 Expands to Account for Variability
Cleaning Validation
Cleaning validation is an integral part of verification of the suitability of the manufacturing process in pharmaceutical manufacturing. Analytical …[Read more...]about Cleaning Validation
New Regulations on USP 232/233: Elemental Impurities in Drug Products
The FDA is requiring compliance of drug manufactures to meet the new standards for elemental impurities. These impurities include those that are …[Read more...]about New Regulations on USP 232/233: Elemental Impurities in Drug Products
Cohort of Concern
Toxicological risk assessments are often geared towards designating the safe levels of exposure to individual chemicals and compounds for humans. With …[Read more...]about Cohort of Concern
