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BEGIN:VEVENT
CLASS:PUBLIC
DTSTART;TZID=UTC:20220824T150000
DTEND;TZID=UTC:20220824T160000
DTSTAMP:20220802T061000
UID:MEC-dc2b690516158a874dd8aabe1365c6a0@global-value-web.com
CREATED:20220802
LAST-MODIFIED:20220825
PRIORITY:5
TRANSP:OPAQUE
SUMMARY:Webinar: Regulatory & Quality Expectations After Health Authority Approval
DESCRIPTION:[vc_row][vc_column][mk_image src=”https://global-value-web.com/wp-content/uploads/2022/08/webinar-.png” image_size=”full” link=”https://virtueinsight.com/event/2nd-annual-pharma-innovation-tech-congress-2022/” margin_bottom=”20″][vc_row_inner][vc_column_inner][vc_column_text css=”.vc_custom_1659420725326{margin-bottom: 0px !important;}”]Overview\nThe pharmaceutical life cycle is a complex structure of interconnected processes. A seemingly minor change can have a significant impact on validated processes and regulatory filings.\nLearn from industry experts how to bridge the gap between the operational challenges and regulatory expectations by handling changes throughout the drug product life cycle.\nWhen\nWednesday, 17 August 2022\n15:00h – 16.00h (IST)\n11.30h – 12.30h (CET)\n05.30h – 06.30h (EDT)[/vc_column_text][vc_btn title=”Register Now” shape=”square” color=”warning” size=”lg” link=”url:https%3A%2F%2Fteams.microsoft.com%2Fregistration%2Fmsa5dXf0nE-_1MZZVZuSpg%2CnKi4zA18QE651jXOhZJY0w%2COmNDhLOim0eN-suZlWV9PQ%2CaQluLP-UcEySEon_yMczWA%2CWPjxFDlExUmkBEhrbW6E3A%2CxZ650xlzYU-ztDZPX2CRoQ%3Fmode%3Dread%26tenantId%3D75b9c69a-f477-4f9c-bfd4-c659559b92a6%26skipauthstrap%3D1|title:Register%20Now|target:%20_blank|”][vc_column_text css=”.vc_custom_1659420885437{margin-bottom: 0px !important;}”]\nFree Registration: Click to reserve your seat! ( https://teams.microsoft.com/registration/msa5dXf0nE-_1MZZVZuSpg,nKi4zA18QE651jXOhZJY0w,OmNDhLOim0eN-suZlWV9PQ,aQluLP-UcEySEon_yMczWA,WPjxFDlExUmkBEhrbW6E3A,xZ650xlzYU-ztDZPX2CRoQ?mode=read&tenantId=75b9c69a-f477-4f9c-bfd4-c659559b92a6 )\nAfter registering, you will receive a confirmation email containing information about joining the webinar.\nKey Takeaways[/vc_column_text][mk_custom_list]\n\nStreamlining Change Control Management\nDo & Don’ts to take control of Product Life Cycle\nIdentifying & Overcoming Data gaps across the Product Life Cycle​\nReducing risks, errors, implementation time, and improving profitability.\nMaintaining an effective Quality Management System and Product Quality System\nQMS Regulation and Guidelines – ICH Q8, Q9, Q10, Q11 and Q14\nEngaging with Industry peers and sharing Common Learnings\n\n[/mk_custom_list][/vc_column_inner][/vc_row_inner][vc_column_text css=”.vc_custom_1659420954973{margin-bottom: 0px !important;}”]Who Should benefit?\nFrom C-level executives through Quality VPs, Directors, from managers to the knowledgeable professionals in the lab;\nA shared vision with a milestone on the horizon, visible to all stakeholders, is the recipe for success.\nSession Learnings\nIn this webinar, the attendees learn how to take a holistic view across the value chain and the transition from Regulatory Challenges to Product Life Cycle 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URL:https://global-value-web.com/events/webinar-regulatory-quality-expectations-after-health-authority-approval/
CATEGORIES:Past Events
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