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BEGIN:VEVENT
DTSTART;TZID=Europe/Zurich:20221201T170000
DTEND;TZID=Europe/Zurich:20221201T200000
DTSTAMP:20260403T162015
CREATED:20221005T175157Z
LAST-MODIFIED:20221103T173736Z
UID:1277-1669914000-1669924800@goodlifesci.sidley.com
SUMMARY:Women’s Life Sciences Network Event – Zürich
DESCRIPTION:Digital Health and Artificial Intelligence: Drivers in Transforming the Life Sciences Industry \nJoin us in Zürich for our next Women’s Life Sciences Network event\, which will feature a panel discussion with leading life sciences industry women about the use of artificial intelligence and digital health. \n \nModerated panel discussion: \n\nData augmenting in healthcare\n\n\nChallenges and opportunities in digital health\n\n\nArtificial intelligence in drug development and beyond\n\nSPEAKERS \nFleur Herrenschmidt\nHead Legal Region Europe Pharma\nNovartis \nLisa Kinsella\nVice President and General Counsel\nModerna \nAfua van Haasteren\nManager\, Health Policy and External Affairs\nRoche Diagnostics \nRSVP HERE \n5:00 – 8:00 p.m. CET\nThe panel discussion will be followed by a networking reception and walking dinner. \nFor more information\, please contact Cristina Menendez Ruiz at +32 2 504 6453 or at cmenendezruiz@sidley.com. \nClick here to join the Women’s Life Sciences Network LinkedIn Group. \nJosefine Sommer\nSenior Managing Associate\, Sidley Austin LLP\nWLSN Co-Founder\njosefine.sommer@sidley.com \nTatjana Sachse\nCounsel\, Sidley Austin LLP\nWLSN Lead\ntsachse@sidley.com \nAnna Pavlou\nHead of Legal\, Global R&D and Regulatory at Galderma\nWLSN Co-Founder\nAnna.Pavlou@galderma.com \n\nIn light of the COVID-19 pandemic\, Sidley is taking precautions to safeguard the well-being of our clients\, colleagues\, and guests. We encourage you to practice social distancing and follow local guidelines. If you are experiencing cold- or flu-like symptoms or if you have been in contact with anyone who has been exposed to or infected with COVID-19 within the past 14 days\, please refrain from attending this event. We appreciate your cooperation and concern for the health and safety of our guests.
URL:https://goodlifesci.sidley.com/event/womens-life-sciences-network-event-zurich/
LOCATION:Kraftwerk\, Selnaustrasse 25\, Zürich\, 8001\, Switzerland
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Los_Angeles:20221025T133000
DTEND;TZID=America/Los_Angeles:20221025T183000
DTSTAMP:20260403T162015
CREATED:20220922T163821Z
LAST-MODIFIED:20220922T224245Z
UID:1262-1666704600-1666722600@goodlifesci.sidley.com
SUMMARY:Life Sciences Regulatory Bootcamp
DESCRIPTION:Building a foundation for success in the medical products industry\n\nJoin us for an afternoon of discussions designed to provide a foundation in FDA\, healthcare\, and securities issues arising in the development of medical products. Whether you are relatively new to counseling and risk mitigation in these areas or more experienced counsel looking for an efficient way to focus on their application in pre-commercial contexts\, this event is for you. Learn from Sidley’s experienced regulatory and disclosure lawyers and get answers to your most pressing questions. \n \nWho Should Attend: Lawyers needing a practical introduction to legal and regulatory issues arising in the development of medical products. \nFEATURED PANELS \nEssential FDA Concepts and Strategic Considerations for Drug Development \n\nFDA’s expectations of drug developers\nFDA programs to expedite development and regulatory review\nNon-patent exclusivities administered by FDA: considerations for lifecycle management and mitigating litigation risks\nDisputing FDA Actions\n\nProcedural options and definition of success\nKey factors predicting outcomes\nAppropriate means of influencing FDA\n\n\n\nEngagement with Patients and HCPs\, Including Compliance Considerations for Pre-Commercial Products \n\nObtaining coding\, coverage\, and reimbursement\nPricing considerations\nMarket access strategies\, including expanded/post-trial access\nArrangements with HCPs and patients\nRight-sized compliance infrastructure\n\nPractical Approaches to SEC\, Shareholder Litigation\, and FDA Risks in Pre-Approval Communications \n\nSEC and FDA requirements/coordination with respect to pre-approval communications and disclosures for public life science companies\nIssues and trends in shareholder litigation\nPractical approaches to mitigating regulatory\, enforcement\, and litigation risks\n\nRSVP HERE \n1:30 p.m. – 5:30 p.m. PT | Cocktail Reception: 5:30 p.m. – 6:30 p.m. PT \n\nCLE credit for this program is pending. \nFor more information\, contact Sidley Global Life Sciences.
URL:https://goodlifesci.sidley.com/event/life-sciences-regulatory-bootcamp/
LOCATION:Sharon Heights Country Club\, 2900 Sand Hill Rd\, Menlo Park\, CA\, United States
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20220922T160000
DTEND;TZID=America/New_York:20220922T180000
DTSTAMP:20260403T162015
CREATED:20220825T230546Z
LAST-MODIFIED:20220826T185216Z
UID:1219-1663862400-1663869600@goodlifesci.sidley.com
SUMMARY:Women’s Life Sciences Network Event – Boston
DESCRIPTION:Join us for our first U.S.-based Women’s Life Sciences Network event in Cambridge\, a center of life sciences and technology. Keynote speaker Lara Sullivan\, President and CEO of Pyxis Oncology\, will share and discuss hot topics in the industry – followed by a networking reception with cocktails and hors d’oeuvres. \n \nClick here to join the Women’s Life Sciences Network LinkedIn Group. \nFor more information\, please contact Sidley Global Life Sciences. \nDonielle McCutcheon\nPartner\, Healthcare\nWLSN Boston Co-Leader\ndmccutcheon@sidley.com \nAdriana V. Tibbitts\nPartner\, Technology and Life Sciences Transactions\nWLSN Boston Co-Leader\natibbitts@sidley.com \nJosefine Sommer\nSenior Managing Associate\, Food\, Drug and Medical Device Regulatory\nWLSN Co-Founder\njosefine.sommer@sidley.com \n\nIn light of the COVID-19 pandemic\, Sidley is taking precautions to safeguard the well-being of our clients\, colleagues\, and guests. If you are experiencing cold or flu-like symptoms or if you have been in contact with anyone who has been exposed to or infected with COVID-19 within the past 14 days\, please refrain from attending this event.
URL:https://goodlifesci.sidley.com/event/womens-life-sciences-network-event-boston/
LOCATION:The Royal Sonesta | Studio Patio\, 40 Edwin H Land Blvd\, Cambridge\, MA\, 02142\, United States
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Zurich:20220906T133000
DTEND;TZID=Europe/Zurich:20220906T170000
DTSTAMP:20260403T162015
CREATED:20220627T182830Z
LAST-MODIFIED:20220629T160431Z
UID:1111-1662471000-1662483600@goodlifesci.sidley.com
SUMMARY:Swiss MedTech 2022 and Beyond: Mitigating Risks
DESCRIPTION:Please join Sidley and ISS AG in Bern for an afternoon of practical tips and interactive discussions on current issues\, including: \n\nBridging regulatory gaps across the EU\, UK\, and Switzerland\nManaging risks associated with new developments\n\n \nIndustry speakers\, regulators\, scientific experts\, and counsel will share tips and best practices for the challenges and opportunities that lie ahead for Swiss MedTech enterprises. \nLocation \n\nHotel Schweizerhof | Bahnhofplatz 11 | 3001 Bern \nRegister here \n1:30 p.m. – 5:00 p.m. CET\nCocktail reception to follow \nView agenda here \n\nTopics include: \n\nSustainability\nDigital Health\nCybersecurity\n\nWho should attend? \nExecutives\, investors\, in-house counsel\, and regulatory managers interested and/or facing regulatory issues in Switzerland. \n\nFor more information or questions\, please contact gvaevents@sidley.com. \nIn light of the COVID-19 pandemic\, Sidley is taking precautions to safeguard the well-being of our clients\, colleagues\, and guests. If you are experiencing cold- or flu-like symptoms or if you have been in contact with anyone who has been exposed to or infected with COVID-19\, please refrain from attending this event. \nSidley Austin LLP and ISS AG will process delegate contact details for the purposes of organizing and administering this event and for contacting you about future events. Please note that delegate contact details may be passed between Sidley Austin LLP and ISS AG for the above purposes.
URL:https://goodlifesci.sidley.com/event/medtech-2022-and-beyond-mitigating-risks/
LOCATION:Hotel Schweizerhof\, Bahnhofplatz 11\, Bern\, Switzerland
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20220712T133000
DTEND;TZID=America/New_York:20220712T163000
DTSTAMP:20260403T162015
CREATED:20220614T190519Z
LAST-MODIFIED:20241115T214007Z
UID:1082-1657632600-1657643400@goodlifesci.sidley.com
SUMMARY:Boston Life Sciences Roundtable
DESCRIPTION:Please join us for Sidley’s first in-person Boston Life Sciences Roundtable program\, an afternoon of provocative discussions addressing cutting-edge trends and topics. \nTuesday\, July 12\, 2022 \n1:30 p.m. – 4:30 p.m.\nCocktail reception to follow \nFeatured Panels \nLeading Life Sciences Companies: A Conversation with Boston Area General Counsel \nGina Mazzariello\, Chief Legal Officer & General Counsel\, Amylyx Pharmaceuticals\, Inc.\nKaren Tepichin\, General Counsel\, Ginkgo Bioworks\nJoe Vittiglio\, Chief Business and Legal Officer\, Finch Therapeutics\, Inc.\nScott Kaplan\, Partner\, Food\, Drug and Medical Device Regulatory and former FDA Associate Chief Counsel\, Enforcement\nBecky Wood\, Partner\, Food\, Drug and Medical Device Regulatory and former FDA Chief Counsel \nLessons from the Trenches – Navigating FDA\, SEC\, and Strategic Issues in Product Development and Commercialization Messaging \nPamela Connealy\, Chief Financial Officer\, Pyxis Oncology\nHeather Turner\, former Chief Legal Officer\, Lyell Immunopharma\, Inc.\nStephen Cohen\, Partner\, Securities Enforcement and Regulatory\nTorrey Cope\, Partner\, Food\, Drug and Medical Device Regulatory\nFrank Rahmani\, Partner\, Capital Markets \nDown\, But Not Out – Dealing With a Challenging Capital Environment \nChristian Schade\, Chairman and Chief Executive Officer\, Aprea Therapeutics\nGeoff Levin\, Partner\, Private Equity\nAsher Rubin\, Partner\, Technology and Life Sciences Transactions \nKeynote Presentation \nNatalie Silverstein\, M.P.H. \nNatalie Silverstein is an author\, speaker\, consultant and passionate advocate for family and youth service. She is the author of two books about giving back and kindness\, including Simple Acts: The Busy Family’s Guide to Giving Back\, and most recently Simple Acts: The Busy Teen’s Guide to Making A Difference. \nAdditional panelists to be announced. \n\nWHO MAY BE INTERESTED IN ATTENDING \nExecutives\, Investors\, General Counsel\, and Company Counsel \nABOUT THE PROGRAM \nThe Boston Life Sciences Roundtable is an annual event designed to address cutting-edge trends and hot topics in the life sciences sector. Sidley hosts an annual Life Sciences Roundtable in San Francisco and now in Boston. \nFor more information\, contact globallifesci@sidley.com. \nCOVID-19 PROTOCOL \nIn light of the COVID-19 pandemic\, Sidley continues to take precautions to safeguard the health and well-being of our clients\, colleagues\, and guests. Proof of vaccination is required to attend. If you are experiencing cold- or flu-like symptoms or if you have been in contact with anyone who has been exposed to or infected with COVID-19 within the past 14 days\, we ask that you not attend the event. We appreciate your cooperation and concern for the health and safety of our guests. \nAdditional guidance will be provided prior to the event and in accordance with CDC and local guidelines.
URL:https://goodlifesci.sidley.com/event/boston-life-sciences-roundtable/
LOCATION:MassBio\, 700 Technology Square 5th floor\, Cambridge\, MA\, 02139\, United States
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Los_Angeles:20220622T133000
DTEND;TZID=America/Los_Angeles:20220622T163000
DTSTAMP:20260403T162015
CREATED:20220517T154519Z
LAST-MODIFIED:20220621T181704Z
UID:1031-1655904600-1655915400@goodlifesci.sidley.com
SUMMARY:Bay Area Life Sciences Roundtable
DESCRIPTION:Please join Sidley at SFMOMA for the 7th Annual Bay Area Lifesciences Roundtable\, an afternoon of provocative discussions addressing cutting-edge trends and hot topics. \nWe are thrilled to be back together in-person for this year’s event which will be held at a beautiful outdoor space—SFMOMA’s Sculpture Garden. \n \nRSVP \nWednesday\, June 22\, 2022\n1:30 p.m. – 4:30 p.m.\nCocktail reception to follow \nPrivate access to the Fisher Collection and the Contemporary Optics Exhibit will be available during the cocktail reception. \n\nFEATURED PANELS \nAdditional panelists to be announced. \nHot Topics in Managing Global Supply Chain Issues: Before\, During\, and After Launch\nGain valuable insights from in-house and former agency counsel who have been in the trenches. \nTopics will include: \n\nCommon global supply chain patterns for pre-commercial and commercial companies\nHow to manage FDA compliance and quality risks associated with global supply chain\nEvaluating key international reference pricing considerations and trends\nAnalyzing key case study examples\n\nFeatured Panelists \nAngie Lewis-White\, VP Commercial Supply Chain & Contract Manufacturing\, Myovant Sciences \nRaj Pai\, Partner\, Food\, Drug and Medical Device Compliance and Enforcement; formerly with the FDA’s Office of Chief Counsel and former Special Assistant United States Attorney \nCatherine Starks\, Partner\, Healthcare \nAdriana Tibbitts\, Partner\, Technology and Life Sciences Transactions \n  \nOperationalizing Diversity for Positive Business and Clinical Results\nDiversity is a laudable goal\, sufficient in its own right. However\, this panel will take the topic a step further\, exploring concrete ways that diversity can be used to make and run a better life sciences company. \nTopics will include: \n\nExamining diversity in clinical trial design and recruitment to lead to better medicines\nSteps to ensure that market access strategies deliver innovative products to appropriate\, but often underserved\, groups who would benefit\nThe myriad ways that diversity touches how companies operate\, from the board room to the lunch room\n\nFeatured Panelists \nStanley Lewis\, MD\, Founder and CEO of A28 Therapeutics \nBrandon Allgood\, Ph.D.\, Chief Artificial Intelligence Officer\, Valo Health \nR’Kes Starling\, Chief Executive Officer/President\, Reveles Clinical Services \nDeeona Gaskin\, Partner\, Food\, Drug and Medical Device Compliance and Enforcement \nModerators \nStephen Abreu\, Partner\, Technology and Life Sciences Transactions \nMustafa Abdul-Jabbar\, Managing Associate\, Commercial Litigation and Disputes \n  \nManaging Your Message and Positioning: Navigating Strategic and Disclosure Considerations in Product Development and Launch\nDeciding when and how to share non-public information about key events in your company’s life cycle in general and in transactional settings—such as clinical trial results\, regulatory meetings\, and product launch—raises complex questions at the intersection of SEC\, FDA and First Amendment law. Our panel will help you: \n\nUnderstand expectations from key federal regulators\, with insights from seasoned practitioners\, including former FDA Chief Counsel\nTrack evolving First Amendment protections for truthful and non-misleading commercial and scientific speech\nExplore real-world scenarios\, including: preparing for data release from clinical trials\, charting next steps and regulatory pathways\, and evaluating public statements about comparative and competitive positioning\, regulatory meetings\, and feedback\nUnderstand the perspectives of seasoned practitioners and in-house counsel about managing disclosures in transactional settings\, IPOs\, and M&A\n\nFeatured Panelists \nHeather Turner\, former Chief Legal Officer\, Lyell Immunopharma\, Inc. \nFrank Rahmani\, Partner\, Global Life Sciences and Capital Markets \nBecky Wood\, Partner\, Food\, Drug and Medical Device Regulatory and former Chief Counsel\, FDA \n\nCOVID-19 PROTOCOL \nIn light of the COVID-19 pandemic\, Sidley continues to take precautions to safeguard the health and well-being of our clients\, colleagues\, and guests. Proof of vaccination is required to attend. Please follow all CDC and local California guidelines. If you are experiencing cold- or flu-like symptoms or if you have been in contact with anyone who has been exposed to or infected with COVID-19 within the past 14 days\, we ask that you not attend the event. We appreciate your cooperation and concern for the health and safety of our guests. \nAdditional guidance will be provided prior to the event and in accordance with CDC and local guidelines. \n\nWho may be interested in attending \nExecutives\, Investors\, and Company Counsel \nCLE credit for this program is pending. \nFor more information\, contact GlobalLifeSci@sidley.com.
URL:https://goodlifesci.sidley.com/event/bay-area-life-sciences-roundtable/
LOCATION:SFMOMA\, 147 Minna St. Floor 5\, San Francisco\, CA\, 94103\, United States
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END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20220622
DTEND;VALUE=DATE:20220624
DTSTAMP:20260403T162015
CREATED:20220608T201642Z
LAST-MODIFIED:20220608T203139Z
UID:1063-1655856000-1656028799@goodlifesci.sidley.com
SUMMARY:Digital Health App'ero and Life Sciences College
DESCRIPTION:Digital Health App’ero \nOn the eve of the Life Sciences College 2022\, we welcome you to our first Digital Health App’ero\, which will feature a panel discussion with key industry representatives on the use of digital health tools by pharma and medtech companies. The panel will be followed by a networking forum for professionals in this space. \nStaying Ahead of the Curve – Issues on the Radar for Pharma and Medical Devices Companies \nPlease join us for our annual life sciences legal conference\, bringing together senior members of the European Commission and industry thought leaders. This edition will focus on a variety of topics\, including the latest regulatory developments in the EU and the outlook for the life sciences industry as a whole. This year’s keynote address will be presented by Andrezj Rys\, Director responsible for Health Systems\, Medical Products and Innovation\, Directorate General for Health and Food Safety (DG Sante)\, European Commission. \nAgenda \nLocation \n\nDigital Health App’ero\nTHE HOTEL – Bd. de Waterloo 38\, 1000 Bruxelles\n6:00 p.m. – 7:30 p.m.\nFollowed by networking drinks \nStaying Ahead of the Curve – Issues on the Radar for Pharma and Medical Devices Companies\nTHE HOTEL – Bd. de Waterloo 38\, 1000 Bruxelles\n8:30 a.m. – 5:10 p.m. followed by networking drinks\nBreakfast will be served from 8:30 a.m. \nRegister here for both events. \n\n\nThe event is open to in-house counsel\, regulators\, and regulatory personnel at pharmaceutical and medical devices companies. There is no registration fee to attend this event. For more information\, please contact Cristina Menéndez Ruiz at +32 2 504 6453 or cmenendezruiz@sidley.com. \nIn light of the COVID-19 pandemic\, Sidley is taking precautions to safeguard the well-being of our clients\, colleagues\, and guests. If you are experiencing cold or flu-like symptoms or if you have been in contact with anyone who has been exposed to or infected with COVID-19\, please refrain from attending this event. \n\nKey takeaways from Life Science College 2021 are available here. \nTrendspotting 2022: On the Pulse of Life Sciences
URL:https://goodlifesci.sidley.com/event/digital-health-appero-and-life-sciences-college/
LOCATION:THE HOTEL\, Bd. de Waterloo 38\, 1000 Bruxelles\, Brussels
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20220518T080000
DTEND;TZID=America/New_York:20220519T160000
DTSTAMP:20260403T162015
CREATED:20220428T171425Z
LAST-MODIFIED:20220506T200842Z
UID:845-1652860800-1652976000@goodlifesci.sidley.com
SUMMARY:Regulatory Reboot: What You Need to Know About Biopharma Regulation in 2022 and Beyond
DESCRIPTION:Join Sidley for a two-day program designed to provide a sophisticated\, comprehensive foundation in regulatory law for in-house lawyers involved in biopharma development\, manufacturing\, and marketing. Whether you are relatively new to regulatory counseling and risk mitigation or more experienced counsel looking for an efficient way to catch up on developments in the law from the past two years\, this event is for you. By the end of the second day\, you’ll have the information and insights you need to tackle any biopharma regulatory issue and know when to worry\, whom to call\, and how and when to scale up. \n \n\nLearn from Sidley’s most experienced biopharmaceutical regulatory lawyers and head back to work with high-quality substantive materials to make your job easier.\nGet to know your instructors and peers during breaks and over dinner — networking is risk management.\nCome as you are — we will provide the conditions you need for a comfortable\, productive learning experience\, from an on-demand barista to comfortable seating\, great tech\, and high-end supplies.\nIf need be\, catch up on work in our newly refurbished\, sunny\, spacious break-out rooms.\n\nClick here to view the full agenda. \nWednesday\, May 18\, 2022 \nFEATURED SESSIONS \n\nDrug Development — Clinical Trials\, Biostatistics\, Real-World Evidence\, and Disputes\nEthics — Ethics Issues Arising in FDA Regulatory Contexts\nStatutory Exclusivities\nAKS/Fraud & Abuse\n\nThursday\, May 19\, 2022 \nFEATURED SESSIONS \n\nSupply Chain Essentials — DSCSA\, PDMA\, GMP\nPublic Company Disclosure Issues — Regulatory and Enforcement (FDA and SEC)\, Class Actions\nEthics Issues Arising in FDA Regulatory Contexts\n\nWHO SHOULD ATTEND \nIn-house counsel with responsibility for regulatory compliance\, analysis\, engagement\, and risk mitigation. \n\nRegister here \nWednesday\, May 18\n8:00 a.m. – 4:30 p.m.\nReception follows: 4:30 p.m. – 6:30 p.m. \nThursday\, May 19\n8:00 a.m. – 4:00 p.m. \n\nCLE credit for this program is pending. \nFor more information\, contact globallifesci@sidley.com.
URL:https://goodlifesci.sidley.com/event/regulatory-reboot-what-you-need-to-know-about-biopharma-regulation-in-2022-and-beyond/
LOCATION:Sidley’s New York Offices\, 787 Seventh Avenue\, New York\, NY\, 10019\, United States
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20220517T180000
DTEND;TZID=Europe/Brussels:20220517T180000
DTSTAMP:20260403T162015
CREATED:20220428T174524Z
LAST-MODIFIED:20241202T200128Z
UID:851-1652810400-1652810400@goodlifesci.sidley.com
SUMMARY:Women’s Life Sciences Network Event: Global Review of Pharmaceutical Regulations
DESCRIPTION:Join us in Brussels for our next Women’s Life Sciences Network event on the occasion of the EU Pharmaceutical Law Forum. A panel from the International and European pharmaceutical industry associations will share and discuss hot topics in the industry. The panel discussion will include: \n\nGlobal trends on the review of pharmaceutical legislation\nIP rights for innovation and incentives\nMarket access and reimbursement\nRecent antitrust trends\n\nKristine Peers\nGeneral Counsel\nEFPIA \nMelinda Friend\nGeneral Counsel\nIFPMA \n\n\n\n6:00 p.m. CET \nThe panel discussion will be followed by a networking reception and canapés \nSidley Lawyers\nTatjana Sachse | Josefine Sommer \n\nFor more information\, please contact Cristina Menendez Ruiz at +32 2 504 6453 or at cmenendezruiz@sidley.com. \nClick here to join the Women’s Life Sciences Network LinkedIn Group. \nIn light of the COVID-19 pandemic\, Sidley is taking precautions to safeguard the well-being of our clients\, colleagues\, and guests. If you are experiencing cold or flu-like symptoms or if you have been in contact with anyone who has been exposed to or infected with COVID-19 within the past 14 days\, please refrain from attending this event.
URL:https://goodlifesci.sidley.com/event/womens-life-sciences-network-event-global-review-of-pharmaceutical-regulations/
LOCATION:Comet\, Place Stephanie 50\, Brussels\, 1050\, Belgium
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