Find your missing element at DCAT Week 2024

March 18-21, 2024 | New York City, New York

Strategically moving from molecule to medicine to market demands trust — trust in your expertise and innovation. Trust in your technology. And above all, trust in the partnership you have with your CDMO. Schedule a meeting with Thermo Fisher Scientific to explore our industry-leading services and solutions for biopharmaceutical companies and learn how we can support your next drug development and manufacturing project.

March 18-21, 2024

In-person

New York City, NY

About DCAT Week

We’re heading to New York City for another exciting DCAT Week, the premier global event for companies engaged in the biopharmaceutical manufacturing value chain. Now in its 96th year, DCAT Week is hosted by the Drug, Chemical & Associated Technologies Association (DCAT), and serves to connect industry professionals and provide them with an unparalleled platform to meet, network, ideate, and collaborate for the year ahead.

Like in years past, we’re honored to sponsor 2024’s DCAT Women's Networking Breakfast on Wednesday, March 20 from 6:45-9 a.m. EDT, one of the most highly anticipated events of the week. In addition to ample opportunity for networking, 2024’s DCAT Women's Networking Breakfast will also feature a keynote presentation from New York Times bestselling author and first team captain of the American Women’s Everest Expedition, Alison Levine.

If you’d like to schedule a private meeting with Thermo Fisher Scientific to explore how our industry-leading CDMO services and solutions can support your next drug development and manufacturing project, you may do so below.

Schedule a meeting

Meet our experts

Thermo Fisher Scientific’s industry-leading subject matter experts Anil Kane, Executive Director, Global Head of Technical and Scientific Affairs, and Christy Eatmon, Global SME, Sterile Drug Products, will both be available at DCAT Week to discuss how our comprehensive CDMO capabilities for small molecules, large molecules, advanced therapies, clinical trial services, and commercial services can help advance your unique drug development and manufacturing journey.

Schedule a meeting

Anil Kane

Christy Eatmon

Find your missing element with Thermo Fisher Scientific

Element

Trust is the foundation of a successful partnership. It allows partners to work as one team, guided by a shared vision, with the confidence that each partner reliably do what they say they will do.

Transparent and open communication is a key element to successful project management. It requires sharing relevant information, feedback, and expectations and it encourages dialogue to address concerns and issues promptly.

Element

An effective partnership is built on mutual respect, open communication, trust, collaboration, and shared objectives, instilling confidence in customers that they will be fully supported along the development journey.

Element

Enabled through tools, technologies, and industry and scientific expertise, foresight enables teams to anticipate and mitigate challenges before they arise.

Element

Navigating the complexities of drug development and manufacturing requires passion, persistence, and unwavering dedication to achieving the shared vision of transforming patients’ lives.

Element

Every project has unique requirements, objectives, and challenges. Close and continuous collaboration is vital for understanding these distinct considerations and tailoring solutions to meet them.

Element

Real-world experience borne from decades of partnering in all aspects of drug development adds critical value to every project above and beyond the advances in sciences and technology that have transformed the industry.

Element

Scientists and subject matter experts with deep understanding of the evolving pharmaceutical landscape provide the skills and perspective to set and keep projects on the path to success.

Element

Scientific, technical, and operational knowledge acquired through deep and wide industry experience is an inimitable competitive differentiator in today’s rapidly evolving industry landscape.

Element

Keeping pace with the rapidly changing pharmaceutical industry requires unprecedented operational agility and flexibility to consistently deliver high-quality, customized solutions.

Insights and resources

Drug development and manufacturing is an ever-changing industry. Stay connected to new discoveries, innovations, and expert scientific opinions.

Whitepaper

Transforming CDMO Partnerships Through Quality

Get an in-depth look into key indicators of CDMO quality, with tools and best practices to drive continuous improvement, strengthen collaboration, and ultimately cultivate trust.

View Infographic

Blog

What is a CDMO? Seven things to look for in a quality CDMO partner

Learn how CDMOs (contract development and manufacturing organizations) work with pharma companies, and the top considerations companies have when choosing a CDMO partner.

Read Blog

Whitepaper

Advancing drug development using in silico modeling

This report provides a framework for that understanding by outlining some of the processes that stand to gain the most from computational modeling and identifying the in silico capabilities that can be used to accelerate and de-risk each phase of development.

Read Whitepaper

Blog

CROs vs CMOs, and CDMOs: What’s the difference between the three?

CROs, CMOs, and CDMOs all help biotechnology and pharmaceutical companies with drug development and manufacturing, but what’s the difference between the three?

Read Blog

Whitepaper

The changing landscape of oncology drug development: Bringing novel lifesaving therapies to patients

Oncology is the fastest-growing, most active sector of drug development. Matching drug products to clinical and commercial needs requires scientific and technological innovation.

View Whitepaper

Blog

Exploring CRDMOs: Reshaping research, development, and manufacturing

CRDMOs, or integrated contract research, development, and manufacturing organizations, are a trend to watch. Discover five benefits of partnering with one.

Read Blog

eBook

Protecting tomorrow: Supporting sustainability in the pharmaceutical and biotech industries

Learn how Thermo Fisher is meeting its environmental sustainability goals, and how we work in partnership with the pharma and biotech communities on shared environmental sustainability goals.

View eBook

Blog

The 5 Drug Development Phases

To be deemed a “success,” a new drug must make it through five specific phases: 1) discovery and development, 2) preclinical research, 3) clinical research, 4) FDA review, and 5) safety monitoring.

Read Blog

Webinar

Optimizing the cell therapy patient journey through integrated CRO CDMO partnership

Watch this on-demand webinar for insights on how working with a single integrated CRO/CDMO partner can help ease industry challenges and provide an accelerated path from development to manufacturing, as well as the benefits that come from unified teams and infrastructure.

Watch Webinar

Infographic

CDMO Checklist to Launch Your Molecule Globally

Preparing to take your drug into the global market? You’ll need to make sure your CDMO has what it takes to successfully navigate the global regulatory space with speed, security, and supply safeguards. Use this quick list as a reference when evaluating your options.

View Infographic

Continuing education for the pharma industry

View insights and resources

Follow us on social media for the latest up-to-date event happenings

Twitter

We look forward to seeing you soon in New York City.

Find your missing element with Thermo Fisher Scientific

Ready to talk about your next project? Contact us now.