Automating pharma labs can present a number of challenges, not only in terms of digitalizing the equipment, workflow and method design, but also in digitizing the documentation of the experiments.
In addition, issues of laboratory efficiency are receiving growing attention as regulatory bodies such as the Food and Drug Administration and Environmental Protection Agency push for processes to be compliant with Good Laboratory Practices (GLP) and an increase of medical products are required as global Covid-19 cases surge.
In this white paper by Merck, discover how to apply the Analytical Information Markup Language (AnIML) to laboratory workflows to better understand how to process digital information and document the analytical data that has been collected throughout the research and development process.
Download the AnIML white paper for solutions in:
- Long-term data storage so scientists can maintain and retain access to data.
- Data interchange to make data sharing, analysis and collaboration much easier.
- Data consistency and workflow standardization.
- Responding efficiently to regulatory requirements so that GLP is upheld.
- How to adopt and deploy AnIML into your laboratory processes.