Connect with innovators, investors, and companies advancing cancer breakthroughs, in person or virtually, during Chicago’s biggest oncology event through the BIO Partnering™ system.
35 events found.
Events
Calendar of Events
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2 events,Why Attend The 2026 SNMMI Annual Meeting will feature: Revolutionary research shaping the future of nuclear medicine and molecular imaging Advanced clinical applications transforming patient care Unparalleled networking opportunities with global thought leaders Who Should Attend? The 2026 SNMMI Annual Meeting will feature groundbreaking research and clinical innovation. This critical event unites physicians, technologists, pharmacists,... |
3 events,
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Taking a recombinant protein from milligrams to GMP-ready scale is where development programs truly succeed or fail. Join this expert-led webinar to explore the critical decision points that impact scalability, quality, CMC readiness, and time to clinic, with real-world insights you can apply immediately. Key learning objectives: - Navigate expression system selection (microbial, mammalian and...
Free
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10 events,
Featured
By invitation only. You must be pre-registered by your Jefferies representative in order to attend. The Jefferies Global Healthcare Conference in New York will take place on Tuesday, June 2 – Thursday June 4, 2026. This year’s conference will focus on life sciences companies in the biotechnology, life sciences tools and services, medical technology, and... Future BioTech Expo is a purpose built international exhibition and conference dedicated to red biotechnology and the science transforming how we prevent, diagnose, and treat disease. Held at the Hilton Houston North on June 2–3, 2026, #FBE26 unites pharma innovators, clinical researchers, biotech CEOs, investors, and policymakers under one roof in one of America's fastest growing...
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At Breakthroughs in Bioprocessing, you'll have the opportunity to: Translate expertise into impact Work alongside Cytiva specialists and industry peers to explore practical, scalable approaches across bioprocess development, manufacturing, and scale-up. Experience innovation beyond theory Engage with advanced technologies in a live, interactive environment designed to support hands-on learning and real-world application. Gain insight through...
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What You'll Learn: How does life sciences continue to be Boston’s and Cambridge's economic engine amid a softening market? With total VC investment at $6.85B across 197 rounds in 2025, is capital concentrating into fewer winners, and how is that changing tenant decision making? Where are AI enabled life sciences users, automation heavy labs, and data...
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This webinar shows how a system-based primary packaging approach—like the West Synchrony™ prefillable syringe system—can streamline tech transfer, simplify GMP qualification, and reduce complexity, cost, and timelines for injectable drug manufacturing. Key Learning Objectives: - How injectable technology transfer impacts project timelines, cost, and risk when working with a CDMO - Where primary packaging decisions...
Free
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8 events,Connecting Translational Science with the Right Partners to Advance Drug Development Join VCs, biopharma decision-makers and academic innovators in Seattle, June 2026, for the 3rd BioCentury Grand Rounds – U.S. This R&D conference brings together leaders at the forefront of translational science to explore the breakthroughs, bottlenecks and strategies shaping the future of drug development.... From data to decisions. From discovery to better patient outcomes. The Festival of Genomics, Biodata & AI returns to Boston at a critical moment for the US life sciences community. Funding pressures, rising development costs and intensifying competition are colliding with an unprecedented opportunity: the convergence of multi-omics, large-scale biodata and artificial intelligence. To stay ahead, organizations must do...
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Reimagine what's possible—together. Join BSI Consulting for an expert-led forum designed for pharma and biotech professionals who are shaping the next era of EHS. Connect with peers, challenge assumptions, and explore practical solutions to the industry's most pressing risks and opportunities. This event brings together leaders at the forefront of life sciences in EHS to...
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The webinar also highlights the growing role of AI within regulated manufacturing environments. Rather than treating AI as an add-on, the session outlines how to embed it into validated frameworks to support predictive maintenance, yield optimization, and faster product release cycles.
Free
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CHO expression continues to evolve, and recent advances are reshaping how quickly and efficiently high-performing cell lines are developed. In this webinar, experts explore the latest innovations in the GS® Expression System, highlighting how advanced vector design, stronger selection stringency, and enhanced promoter control are driving higher titers, more stable pools, and faster timelines from...
Free
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10 events,Dive into the future of aging with cutting-edge AI breakthroughs at this can’t-miss summit! June 4–5, 2026 | BioLabs@NYU Langone, Long Island City, Queens Longevity science is at an inflection point. Foundation models are learning the language of biology, aging clocks are quantifying human health with new precision, and a generation of therapeutics and clinical... Join us for our 33rd Annual MDC, which features engaging panel sessions and keynote addresses, a Partnering Hall connecting attendees with start-ups and investors from around the globe, the MedTech Innovator pitch event, and a lively wine tasting reception where venture capitalists serve as sommeliers.
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MassBioEd’s Annual Life Science Workforce Conference brings together representatives from the life sciences industry, academic institutions, training providers, government and community to explore key issues and strategies in building a strong life science workforce in Massachusetts. The 2026 Life Sciences Workforce Conference: Building Talent Pathways in a Dynamic Time: Massachusetts Prepares the Future Workforce will be held...
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Immune checkpoint inhibitors have transformed cancer treatment, but response rates remain limited, and immune-related toxicities continue to pose challenges. Gene editing of therapeutic T cells offers a promising path to help enhance specificity and safety by directly modulating checkpoint expression. In this webinar, we explore how gene-edited T cells targeting PD-1 and TIGIT can improve...
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Technology transfer to a CDMO is rarely as simple as handing over a data package. From documentation gaps and equipment differences to method variability and global standards, many programs encounter avoidable risks that can derail timelines and increase cost. In this Outsourced Pharma Live session, industry experts share practical strategies to help sponsors better prepare...
Free
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1 event,CYTO 2026, the 39th annual Congress of the International Society for the Advancement of Cytometry, is the premier, inclusive, and international conference on the many facets of cytometry science and engineering. Guided by this year's theme, Cytometry: The Next Wave, the meeting will showcase groundbreaking innovations and emerging directions shaping the field. Join us in West... |
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2 events,
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In this webinar, Lonza experts share insights from 70+ bispecific programs, revealing the most common early‑stage risks across analytical development, downstream purification, and drug product formulation. You’ll learn where challenges typically emerge before IND, how early decisions shape CMC readiness, and when to rely on platform approaches versus molecule‑specific strategies to avoid costly delays. Key...
Free
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2 events,
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This webinar breaks down how evolving expectations under ICH Q5A(R2) are reshaping viral detection strategies, shifting the industry from targeted testing toward broader, more sensitive approaches. Through real‑world examples, you’ll learn where current methods fall short, how newer technologies expand visibility, and how teams can strengthen viral safety programs without disrupting development timelines or regulatory...
Free
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2 events,
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IND submission is a critical milestone in mAb development — but analytical methods established at this stage must ultimately support validation, tech transfer, and evolving regulatory expectations. Among these, residual host cell DNA quantitation assays play a central role in monitoring residual impurity levels, supporting process performance, and may help reduce downstream risks. This webinar...
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We are very excited to invite you to our BVS, in collaboration with JLL Biotech Community Innovation Night at 115 Munson! Mark your calendars for a great opportunity to connect with industry leaders, explore innovative products, and mingle with fellow professionals in the biotech community. We are inviting all research scientists from the institutes, biotech... |
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1 event,The DIA Global Annual Meeting is where life sciences professionals from industry, regulatory agencies, patients, and academia come together to drive breakthroughs in healthcare — advancing science, policy, and patient outcomes worldwide. |
2 events,
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Explore how advanced nanoparticle engineering is transforming formulation across both small and large molecule modalities. Dr. Chris Worrall highlights how Nanoform’s technologies enable higher drug‑loading oral tablets, ultra‑high‑concentration biologic formulations for SubQ delivery, and new possibilities for pulmonary administration. Through real case studies, you’ll see how nanoforming can reduce pill burden, unlock patient‑friendly alternatives to...
Free
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4 events,
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Increasing titers isn’t the only way to maximize process efficiency. Whether you’re optimizing an existing process or developing the next generation of biologics, we can help you identify the levers that matter most. Join us for an interactive discussion on the process decisions, tradeoffs, and operational realities shaping modern biologics manufacturing. Bioprocess Online’s Tyler Menichiello...
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In this session, leading cell therapy CDMOs will break down how they support programs across development—from early process work through GMP manufacturing, scale-up, and commercial readiness—and where different approaches can reduce downstream risk or introduce it. This is a focused look at who does what, and where they fit—so you can evaluate partners with greater...
Free
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In this session, leading CDMO experts will break down the key decisions across host cell selection, vector design, and clone screening strategies, and explain how those choices impact expression, scalability, and long-term manufacturability. These presentations will highlight how different CDMO approaches can reduce downstream risk or introduce it, as programs move from early development into...
Free
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5 events,
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What You’ll Learn: Gain insights into how renewed leasing activity, selective capital and improving absorption are reshaping demand, investment, and development decisions across the Bay Area life sciences market. Learn how owners, developers, and operators are rethinking space utilization, right sizing portfolios, and repositioning existing assets to meet today’s tenant expectations. Examine why South San...
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Clinical trials sit at a unique intersection of science, patients, and clinical care, and for decades, the “gold standard” has prioritized the rigor of the data, often at the expense of the patients providing it. This gap between rigid protocol requirements and the realities of patients' lives is a primary driver of participant hesitancy and...
Free
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Join us for this digital event designed for pharmaceutical and biopharmaceutical companies seeking reliable CDMO partnerships to accelerate their microbial programs from development through commercial manufacturing. By attending this digital event, you will learn how these capabilities come together to support efficient development, smooth scale-up, and consistent production. The presentations will also provide insight into...
Free
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4 events,
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Featured
Difficult to purify small molecules pose a big challenge for drug developers. Working with a CDMO that has specialized expertise in chromatography ensures that no matter the purification challenges or scale, your program can be taken care of. Learn more...
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Given its inherent time and resource demands, variability in productivity, and the rising complexity of monoclonal antibody (mAb) modalities—including bispecific antibodies (bsAb) and fusion proteins—cell line development (CLD) has become a leading constraint on bioprocess development. Designed to address these constraints, the Gibo™ CHOvantage™ GS CLD kit is a transposon-based CHO-K1 CLD platform that offers...
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A summer outing that actually does something. Bases & Breakthroughs is built for teams. It’s an easy, high-energy way for life science companies and supporters to invest in Philadelphia while giving employees, clients, partners, and colleagues a memorable night out at the ballpark. Your ticket includes access to our pregame hospitality experience at Citizens Bank... |
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1 event,Celebrate 10 years of biotech innovation at UCLA. Explore the future of AI in medicine with VCs, founders, and industry leaders. For the past decade, SoCal TBA has connected the biotech communities of Southern California and Taiwan. This year’s theme, “From Foundations to Frontiers: AI, Innovation, and the Future of Biomedicine,” brings together leaders in... |
4 events,
Featured
The industry’s premier event hosts thousands from across the global biotech ecosystem. Four days of programming, networking, Company Presentations, and BIO Partnering™ focus on the future of our industry and make this a must-attend event. BIO 2026 is where we return to this essential "why." It is our opportunity to reconnect as a global community, to recharge...
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As biomanufacturers face increasing pressure to boost productivity, reduce costs, and accelerate timelines, traditional scale-up approaches can introduce variability and performance drift. Intensified upstream processing offers a more scalable, efficient path forward—helping maintain product quality, process stability, and regulatory compliance from development through GMP manufacturing. In this webinar, Thermo Fisher Scientific experts share best practices...
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Study build inefficiency is rarely caused by a single failure point. Instead, delays accumulate across fragmented protocol interpretation, manual configuration, iterative amendments, and validation cycles that often surface issues late—when they are more costly to resolve. For many sponsors and CROs, this has become the accepted baseline. The more important question is whether it needs...
Free
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Biocom is pleased to announce our upcoming Venture Hub Showcase—an international pitch event taking place during the 2026 BIO International Convention. This event offers a valuable opportunity to connect with potential strategic partners and investors, while exploring the latest life science innovations from fellow industry leaders. Light snacks and refreshments will be provided. |
5 events,
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Bioprocess Online's Bio-Expo Live is back with its series of live virtual events designed to empower biopharma professionals. Through these sessions, attendees will have the chance to explore the newest equipment and solutions offered by our presenters, aimed at addressing the current challenges within the drug development process. This interactive online platform ensures convenience and... 
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Featured
This webinar explores why inspection in HMLV environments is inherently challenging and identifies the most common pain points faced by operations, engineering, and quality teams.
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As cell therapy programs transition into clinical development, manufacturing teams face increasing pressure to automate workflows while preserving biological performance and hard-earned process knowledge. Many teams hesitate to introduce automation due to concerns around forced process redesign, loss of flexibility, or risks to clinical timelines. In this webinar, Cytiva specialists will demonstrate how the Sefia™... |
3 events,
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Bioprocess Online's Bio-Expo Live is back with its series of live virtual events designed to empower biopharma professionals. Through these sessions, attendees will have the chance to explore the newest equipment and solutions offered by our presenters, aimed at addressing the current challenges within the drug development process. This interactive online platform ensures convenience and...
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As sterile pharmaceutical manufacturing evolves, isolators and Restricted Access Barrier Systems (RABS) have become central to contamination control strategies across global markets. Yet regulatory expectations from the FDA, EU GMP Annex 1, PIC/S, and WHO differ in meaningful ways, from legal enforceability to technical prescriptiveness, creating compliance complexity for manufacturers supplying multiple markets. This webinar...
Free
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4 events,
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Bioprocess Online's Bio-Expo Live is back with its series of live virtual events designed to empower biopharma professionals. Through these sessions, attendees will have the chance to explore the newest equipment and solutions offered by our presenters, aimed at addressing the current challenges within the drug development process. This interactive online platform ensures convenience and...
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False rejects are more than a nuisance—they create unnecessary waste, disrupt production efficiency, and erode confidence in inspection systems. In this webinar, we will explore the top 10 causes of false rejects across system setup, environmental conditions, and product and operational variability. We will also demonstrate why false rejects are not inevitable, but instead indicators... 
Featured
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Featured
In this webinar, Revvity Signals will explore how Signals Clinical applies governed, fit-for-purpose AI within clinical data review workflows. The discussion will focus on practical ways to accelerate review while keeping clinical experts in control. |
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2 events,
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Once a fringe idea in chemical biology, targeted protein degradation (TPD) has become one of the most watched strategies in drug discovery. TPD has created new therapeutic opportunities for previously undruggable protein targets. Leading experts will discuss the design, challenges, and clinical promise of PROTACs in overcoming limitations of traditional small molecules. Ever wonder: How...
Free
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Residual host cell DNA (residual DNA) is a critical quality attribute across biologics, vaccines and advanced therapy modalities, requiring sensitive and reproducible quantification to support process development, in-process control and lot release. However, traditional workflows can introduce variability and delay release timelines due to reliance on standard curves, multiple manual steps and method complexity. In...
Free
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3 events,
Featured
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Featured
This virtual event will examine manufacturing pain points from process development through commercialization, showing how value driven single use consumable design from the outset helps prevent issues across each stage. 
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The discussion will examine key manufacturing challenges and highlight where consumables add value, where they introduce unnecessary complexity, and how early upstream and downstream decisions impact long-term cost, scalability, and risk. Attendees will leave with key points to consider on how to approach consumables as a strategic part of manufacturing, rather than a line-item cost.
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Rising regulatory expectations and increased scrutiny around particulate contamination are reshaping how risk is managed in bioprocessing. Particulate issues are often identified late in the process, leading to operational disruption, rework, and increased validation burden. This webinar explores how organizations can shift from reactive responses to proactive containment strategies. Using aggregated industry insights and representative... |
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