Everything we do starts with our Mission: to enable our customers to make the world healthier, cleaner, and safer.
Read MoreEverything we do starts with our Mission: to enable our customers to make the world healthier, cleaner, and safer.
Read MoreEverything we do starts with our Mission: to enable our customers to make the world healthier, cleaner, and safer.
Read MoreMaximizing efficiency and reducing bottlenecks across the drug development continuum is critical to delivering life-changing therapies to patients. This is why flexibility – in strategy and solutions – and the power of collaboration are foundational to accelerating drug development, from research through commercialization.
This year at BIO International Convention, we’re showcasing how, through Accelerator™ Drug Development, we tailor our solutions to support our biotech and biopharma customers’ unique needs. We integrate our proven expertise, global reach and broad capabilities – from bioprocessing to clinical supply and clinical research services and manufacturing – to drive the innovation, productivity and scalability that empower the future of drug development.
Watch here for highlights from Thermo Fisher’s BIO International panel discussions on topics ranging from industry trends and sustainability to the power of partnerships and how to break into biotech.
"As a company, we realize that investing in fossil fuel infrastructure now could lock us into a future of high emissions that is incompatible with our climate goals. Acting with urgency is not just a moral imperative—it’s also smart business," says Matthew Yamatin in his interview about his passion for sustainability and how transitioning to a low-carbon economy will create both challenges and opportunities for innovation and growth at Thermo Fisher.
New life-changing medicines could be developed for patients up to 34 months faster, and drug developers could reap the benefits of getting to market quicker, if biotech and biopharmaceutical companies work with a single, integrated service provider instead of the multiple suppliers they now outsource to, according to a new study by the Tufts Center for the Study of Drug Development (CSDD) at Tufts University.
Thermo Fisher plays a pivotal role in bringing new life-changing therapies to patients by supporting our customers with the technologies and expertise that help them push the boundaries of what’s possible. From contract development and manufacturing, to bioprocessing technologies, to clinical research and management of clinical trials, to navigating regulatory approvals and commercial production – our capabilities help customers bring new therapies to market, more swiftly and efficiently than ever.
Cell and gene therapies hold immense promise, but the journey from research to patient care is fraught with challenges, including complex manufacturing, regulatory hurdles, and significant investments.
Navigating these complexities reveals a fundamental truth: no single entity can succeed alone, writes Betty Woo, vice president of cell, gene and advanced therapies at Thermo Fisher.
As part of the BioLabs b.empowered podcast series, Jakob Gudbrand, President, Customer and Commercial Excellence, sat down with Susan Chase, Senior Vice President, Business Development, BioLabs at BIO 2025.
During their brief conversation, Jakob and Susan discussed how Thermo Fisher is accelerating and supporting global life science innovations through R&D, AI, and automation, while highlighting the importance of partnerships and community collaboration to gain speed and momentum in achieving these advancements.
Thermo Fisher Scientific hosted a webinar June 10 to debut an innovative, templated-based process designed to accelerate development of a biologic drug substance – from DNA to Investigational New Drug (IND) / Investigational Medicinal Product Dossier (IMPD) submission and first-in-human clinical trials – in as few as nine months.
Held ahead of BIO International 2025 in Boston, the “Path to IND for Biologics: From DNA to First-in-Human in 9 Months” webinar featured Elena Gontarz, Ph.D., senior manager of R&D projects, drug substance, for Thermo Fisher’s pharma services business. Bernard V. Fallon, vice president of industry programs for BIO, served as the session’s moderator.
WHAT THEY SAID:
Gontarz emphasized that the platformed approach is heavily based on Thermo Fisher’s 30+ years' experience in the biologics space and a multi-year effort to build templates for labs based on real-life data and customer input.
“Regardless of how good we get, we always want to improve – and we want to improve with you [our partners and customers].” - Elena Gontarz
“We’re doing all this to deliver medicines to patients that are really needed and can affect lifespan and life quality.” - Elena Gontarz
KEY TAKEAWAYS:
Feedback from customers and partners has significantly shaped how Thermo Fisher has approached and refined its processes to accelerate the path to IND.
The "Path to IND for Biologics" method gets to the heart of what today’s biotechs need: a robust, fast and high-quality journey to move their molecule from DNA to the clinic.
Investing in powerful technology reduces complexity when developing biologic molecules. For example, this innovative process leverages Artificial Intelligence (AI) and Machine Learning (ML), transposase technology and integrated solutions.
Novel strategies can streamline early development steps of complex biologics, such as Fc-fusion proteins and bispecific antibodies, without sacrificing later development downstream or any key considerations for patients, such as shelf life and potency.
The resulting path to IND the team has developed leverages the breadth and depth of Thermo Fisher’s expertise and capabilities, directly addressing customer asks to:
Provide a broader range of size and scale options
Platform as much as possible
Template documentation processes
Facilitate a seamless transition from drug substance to drug product, packaging, labeling and so on.
When standard solutions aren’t enough, biotech and biopharma companies need a collaborative partner who can design and implement tailored approaches that meet the unique requirements to move their program forward.
Thermo Fisher Scientific participated in a panel discussion today alongside leaders from the pharmaceutical industry to share their experiences in developing sustainability strategies that help them navigate the ever-evolving regulatory landscape.
Held during BIO International and titled “Shaping Strategies for Impact, Resilience and Lasting Value,” the event featured panel participants Michael Cohen, senior director, environmental sustainability for the PPD™ clinical research business of Thermo Fisher Scientific; Andrew Kaplan, senior vice president of U.S. Public Affairs at Takeda Pharmaceuticals; Carol Richardson, ESG and Health Equity Lead at Teva Pharmaceuticals; and Marc Siegel, co-founder of Metrix Advisory.
WHAT THEY SAID:
KEY TAKEAWAYS
Biopharma Leaders of Color (BLOC) attracted a standing-room only crowd during BIO International yesterday with a discussion focused on leadership, innovation and community across the life sciences.
Titled “Innovation in a Changing Environment: Adaptive Strategies,” the panel sponsored by Thermo Fisher Scientific featured Karen Nelson, Ph.D., chief scientific officer, Thermo Fisher; Abbas Kazimi, CEO, Nimbus Therapeutics; Pam Randhawa, founder and CEO, Empiriko; and Dodzie Sogah, Ph.D., chief operating officer, Merida Bioscience. The discussion was moderated by Stephen Abreu, partner, Sidley Austin LLP, and executive director, BLOC.
WHAT THEY SAID:
KEY TAKEAWAYS:
Long-term life science collaborations require cultural alignment, good communication, transparency and more to drive innovation, efficiencies and increase success in bringing new therapies to patients, according to veteran life science executives participating in a fireside chat titled “The Power of Partnerships: Why Long-Term Strategic Collaborations Matter,” at Bio International today.
The panel included Betty Woo, vice president of the cell, gene and advancement therapies business at Thermo Fisher, and Anne Stone, life sciences investor at J.P. Morgan. The conversation was moderated by Monique Knighten, executive director of Portal Houston, a Texas-based network of life science incubators that hosted the discussion at its Boston location.
WHAT THEY SAID:
KEY TAKEAWAYS:
Thermo Fisher Scientific Chairman, President & CEO Marc Casper joined MassBio CEO Kendalle Burlin O’Connell and Mass. Governor Maura Healey for a fireside chat today at BIO International where they highlighted the Commonwealth’s deep industry roots, dynamic innovation ecosystem and unmatched talent pipeline as reasons why the state remains the world’s largest hub for the life sciences.
Titled “Massachusetts. This is the Place,” the discussion offered the perspectives of leaders helping to shape the future of the industry, as well as Casper’s insights on why Thermo Fisher continues to invest in the region, infrastructure and capabilities. Mass. Lt. Governor Kim Driscoll, State Representative and Speaker Pro Tempore Kate Hogan, and several state legislators were also in attendance.
WHAT THEY SAID:
KEY TAKEAWAYS:
Fragmenting regulatory environments, continued risk-aversion in funding, expectations for sustainability and the strategic integration of AI and machine learning in the biotech industry were hot topics Tuesday during “Discussing the Future of Biotech: Innovation, Sustainability, and Growth in a Dynamic Landscape,” a panel at Bio International sponsored and hosted by Thermo Fisher Scientific.
Disruptive innovations expected to improve patients’ lives and a new generation of tech-savvy workers were positive changes expected in the coming years by the panelists, who included Stephen Grant, chief operating officer, Fractional; Parika “Pinky” Petaipimol, vice president of technical operations, Upstream Bio; and Brian Tham, principal consultant, Peregrine Bio. The panel was moderated by Ben Castro, vice president and general manager, large molecule, pharma services, Thermo Fisher Scientific.
WHAT THEY SAID:
The panel highlighted a few disruptive innovations and trends they see in the biotech industry.
KEY TAKEAWAYS:
Panelists shared these recommendations for biotech and pharma companies as the industry looks to the future:
The expert panel shared their optimism for the future, specifically when discussing the younger generation entering the workforce and offered the following career advice for newcomers:
At the heart of many conversations happening throughout BIO International is the biopharma industry’s ever-present need to deliver new therapies to patients faster. In a panel discussion today. titled “Unlocking better outcomes: Where diagnostics meet therapeutics,” collaborators Daniella Cramp, senior vice president and president of Bioproduction at Thermo Fisher, and Joannah Kim, scientific advisor at TrilliumBiO, explained how companion diagnostics, technology and using AI and metadata to add perspective to clinical results, address the need for speed. The discussion was moderated by Betty Woo, vice president, cell, gene, and advanced therapies at Thermo Fisher.
WHAT THEY SAID:
KEY TAKEAWAYS
Thermo Fisher Scientific participated in an interactive discussion Wednesday alongside biotech industry leaders – including educators, physicians and entrepreneurs – to provide students with guidance and connections to help them navigate entry into the biotech industry.
Held during BIO International and titled “Breaking into Biotech,” the event featured speakers Rose Blackburne, vice president, global head of population science strategies and women’s health, Thermo Fisher Scientific; Stacey Hawkins, founder and CEO, Biotech Primer, Inc.; Jeffrey Herrera, associate director, Employee Experience and DEI, Vir Biotechnology, Inc.; Natalie Kuldell, executive director, BioBuilder Educational Foundation; Wyatt McDonnell, Ph.D., CEO and co-founder, Infinimmune; and moderator Leah Lindsey, lead, research and development science philanthropy and community engagement, Takeda Pharmaceuticals.
The leaders shared their personal career journeys and insights, highlighting the tips that aided their own success. After the discussion, students had the opportunity to engage with the panelists through a question-and-answer session.
WHAT THEY SAID:
KEY TAKEAWAYS: