Why is Computer System Validation so important?
As part of the evolving data integrity focus, regulators are closely examining software systems. In particular, auditors are…
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Planning to expand or set up new pharma-biopharma analytical Lab, but high investments becoming…
As the cost of bringing drugs to market continues to grow, time associated with it is reducing day by day, but the expectation…
Confidently Detect and Quantify Mutagenic Impurities in APIs and Drug Products
Mutagenic impurities in APIs and drug products pose a significant risk to health and safety—even in small quantities—and thus are…
How can you comply with USP <1058> AIQ?
Regulated laboratories must demonstrate that analytical instruments are suitable for their intended use. U.S. Pharmacopeia general…
Potential Allergens in Aromatherapy Oils by GC/MS
The European Union (EU) regulates 26 flavor and fragrance allergens. GC/MS is an effective analytical technique for 24 of the 26…
Lowering Detection Limits for Routine Analysis of Pesticides Residues in Foods
Concerns regarding threats to the environment and human health from the use of pesticides have prompted government agencies…
Multiresidue Pesticides Analysis in Food Matrices
Pesticides are vital to the success of crop production. Regulatory agencies have set maximum residue levels (MRLs) for hundreds of…
EXPAND YOUR LAB IN MULTIPLE DIMENSIONS
Tandem mass spectrometry is the undisputed best way to do targeted quantitative analysis. Now take your lab to higher levels of…
Webinar on Metabolomics and Proteomics Approach for comprehensive understanding of Biological…
Due to inherent complexities of biological systems, researchers require multi-pronged strategies to understand and study them.…
Manage Your Lab in One Place
CrossLab iLab core facility management is a web-based enterprise software solution composed of a base software suite and add-on…