November 02, 2021
Many Quality Control (QC) laboratories in pharma and biomanufacturing have not yet achieved digital transformation yet. In fact, many are still using paper and basic generic tools. This leads to cumbersome and time-consuming quality testing. In this webinar our panel of experts will articulate a realistic and achievable vision for QC labs that will help increase productivity for timely batch release while improving data integrity and regulatory compliance.
Join this webinar to learn how to:
- Improving lab efficiency with stepwise test execution to simplify and speed up batch release workflows
- Improving tech transfer through industry standard S88 documentation and execution of methods
- Increasing compliance by eliminating the transcription of data with direct capture from equipment
- Improving QC planning and scheduling by anticipating and controlling load fluctuations in labs, with greater visibility of activities