Reimagine your CDMO partnership

Find your missing element at CPHI Barcelona

Drug development and manufacturing can be a difficult journey, and moving from molecule to medicine comes with challenges. That’s why you deserve a CDMO partner you can trust, every step of the way. Book a meeting with us at CPHI to learn how our key elements of partnership culminate to power success.

Schedule a meeting

October 24-26, 2023

In-person

Fira Barcelona, Spain

Booth 3K50

Event website

We look forward to meeting you in Spain

CPHI Barcelona is the biggest pharma event of the year, making it an ideal opportunity to discover innovation at the source, learn about emerging trends, and connect with experts from around the world.

The event is widely referred to being at the heart of pharma, and we believe that Thermo Fisher Scientific is at the heart of CPHI.

We invite you to schedule a private meeting with us to discover how we can support your drug development and manufacturing journey.

Schedule a meeting

Visit our Expert Café

Subject matter experts from across the Thermo Fisher Scientific global network will be available throughout the conference at our in-booth Expert Café to listen to your needs, answer questions, and help you find the right solutions for your business. Grab a coffee and join an informal discussion about the pressing challenges facing the pharmaceutical industry today or engage in a one-on-one session to get specific insight and guidance to accelerate your drug development journey.

	Tuesday, October 24	Wednesday, October 25	Thursday, October 26
10:00 – 11:00	Oral solid dosage development and manufacturing	CDMO/CRO integration and patient-centered clinical services	Open discussion pharma services (10:00 – 14:00)
11:00 – 12:00	Advanced therapy medicinal products	Oral solid dosage development and manufacturing
13:00 – 14:00	CDMO/CRO integration and patient-centered clinical services
14:00 – 15:00	Aseptic manufacturing and sterile fill-finish	Aseptic manufacturing and sterile fill-finish
15:00 – 16:00	Biologics manufacturing and development	Small molecule active pharmaceutical Ingredient development and manufacturing
16:00 – 17:00	Clinical trial services	Advanced therapy medicinal products

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

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

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

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

Blog

Enabling a digital culture through integrated business processes

In contrast to a physical work environment, where stability and experience are key, a digital business environment focuses on innovation and connectivity. Learn more.

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

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

Infographic

Preparing biologics for commercialization: Understanding Strategies to Reduce Risk and Optimize Outcomes in Drug Development

Within the drug development process, there are several steps that occur between the laboratory and final manufacture of the drug product. Different players step in during each point, so keeping a program with many moving parts on track requires planning and time-tested execution approaches.

View Infographic

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

Continuing education for the pharma industry

View insights and resources

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