Guide to E&L Studies for Drug Manufacturing and Packaging Components
Extractables and leachables analyses, also known as E&L studies, are widely used within the pharmaceutical industry to ensure that a drug product has not absorbed potentially harmful chemicals or compounds during manufacturing, packaging, or storage.
This white paper provides an overview of the process to build and execute successful E&L studies.
To learn more about E&L studies, download the free white paper below.
Guide to E&L Studies for Drug Manufacturing and Packaging Components includes information on
- Why E&L studies are important
- Potential sources of E&L contamination
- E&L testing guidelines
- E&L testing process
- Reducing the risk of E&L contamination