Watch Dr. M. Damodharan from Sai Life Sciences presenting on the topic 'Regulatory Compliance through Instrument Integration and Scientific Data Management'
Dr. M. Damodharan, Chief Quality Officer at Sai Life Sciences participated in a webinar, presenting on the topic Regulatory Compliance through Instrument Integration and Scientific Data Management, organized by the International Society for Pharmaceutical Engineering (ISPE), India.
The webinar titled ‘Regulatory Compliance through Instrument Integration and Scientific Data Management’ is part of the ongoing ‘Pharma Best Practices Webinars’ initiative by ISPE where each webinar features leading subject matter experts covering critical, relevant topics in pharmaceutical manufacturing.
In this webinar, Dr. M. Damodharan presented on the industry-first solution deployed successfully and their benefits in handling instrument integration, data storage, and archival functions and heading towards the fully paperless lab.
Key regulatory requirements and expectations addressed in the presentation:
1. Effective instrument integration in real-time from all types of instruments and all types of file and data formats.
2. Secure storage of the raw data and processed data at the time they are produced,
3. Secure storage and archival of the data for both internal and external audit purposes SDMS- Scientific data management system is the potential solution beyond LIMS, ELN, CDS, and Manual data storage and archival.
As per ISPE, over 1300+ delegate registrations were recorded for this event, which was broadcast live by ISPE on YouTube.