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DTSTART;VALUE=DATE:20251208
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DTSTAMP:20250711T172443Z
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SUMMARY:Biotechgate Digital Partnering
DESCRIPTION:Biotechgate Digital Partnering is designed to support the business development & licensing of Pharma\, Biotech\, Medtech and Digital Health companies. Join five days of virtual partnering and establish new global connections thanks to pre-arranged one-on-one Zoom meetings in our business forum. \nRegister now to take advantage of the platform and request meetings with our global community.
URL:https://thebiocalendar.com/event/biotechgate-digital-partnering-7/
LOCATION:Online
CATEGORIES:Partnering
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DTSTART;TZID=America/Los_Angeles:20251208T110000
DTEND;TZID=America/Los_Angeles:20251208T120000
DTSTAMP:20251106T150415Z
CREATED:20251106T150415Z
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UID:9452-1765191600-1765195200@thebiocalendar.com
SUMMARY:Robust and Cost-Effective mRNA Capping: Critical Quality Attributes and Manufacturing Strategies
DESCRIPTION:This webinar explores the latest advancements in RNA manufacturing\, with a particular emphasis on the scalability of production processes. Special attention is given to capping strategies\, highlighting their critical role in ensuring RNA stability and translational efficiency at industrial scales. Attendees will gain insights into current challenges and innovative solutions for optimizing capping processes in large-scale RNA synthesis.
URL:https://thebiocalendar.com/event/robust-and-cost-effective-mrna-capping-critical-quality-attributes-and-manufacturing-strategies/
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DTSTART;TZID=America/Los_Angeles:20251208T130000
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CREATED:20251110T123336Z
LAST-MODIFIED:20251110T123336Z
UID:9491-1765198800-1765202400@thebiocalendar.com
SUMMARY:Lessons Learned from FDA 483s and Warning Letters – Strengthening GMP Cleanroom Compliance in Life Sciences
DESCRIPTION:Cleanrooms hosting pharmaceutical manufacturing operations are inspected at a critical scale to ensure compliance to regulatory standards. With this comes a responsibility to the manufacturing operations\, quality\, facility maintenance groups and the design professional team to provide a pathway to achieve regulatory approval.  \nWe will explore critical lessons from FDA 483 observations and Warning Letters related to GMP cleanrooms in the life sciences industry. Through real-world case studies and regulatory analysis\, attendees will gain a deeper understanding of common compliance failures—ranging from inadequate contamination control to flawed cleanroom design—and how to proactively address them. Our expertise emphasizes risk-based thinking\, robust documentation practices\, and front-end design strategies to build resilient\, inspection-ready facilities.
URL:https://thebiocalendar.com/event/lessons-learned-from-fda-483s-and-warning-letters-strengthening-gmp-cleanroom-compliance-in-life-sciences/
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