CDMO Companies

RWE Vendor Landscape · CDMO

CDMO Companies in Real-World Evidence

14 to 15 October 2026Hampton Inn by Hilton, Boston Seaport, USA

Contract development and manufacturing organizations (CDMOs) build and make the therapies that real-world evidence ultimately measures, across small molecule, biologics and advanced modalities.

The development and manufacturing partners in the RWE ecosystem meet their buyers at RWE Connect 2026 in Boston.

Put Your Company in Front of 150+ RWE Buyers
Request the sponsorship prospectus. We reply within one business day.

    No public pricing. Enquiry-led, no obligation.

    150+Attendees
    60%Director / VP and Above
    40+Speakers
    200+Meetings Facilitated

    By modality

    What CDMOs Develop and Manufacture

    Contract partners specialise across therapeutic modalities, each with its own science, facilities and quality demands. The strongest cover several.

    Small MoleculeChemically synthesized drugs, the backbone of most portfolios, in oral and sterile forms.Oral & Sterile
    BiologicsAntibodies, proteins and recombinant products made in living cell systems.Large Molecule
    Cell & Gene TherapyAutologous and allogeneic advanced therapies (ATMPs) with complex logistics.Advanced Therapy
    Antibody-Drug ConjugatesTargeted payloads combining biologic and small-molecule chemistry.Complex / ADC
    Sterile Fill-FinishAseptic filling, lyophilization and final packaging of injectables.Injectables
    Vaccines & PlasmaProphylactic and plasma-derived biologics manufactured at scale.Biologics

    Evaluation

    What Makes a Strong CDMO Partner

    Sponsors weigh development and manufacturing partners against a demanding bar. These are the criteria that decide who wins the contract.

    Quality & Compliance RecordA clean FDA and EMA inspection history and a mature quality system.
    Capacity & ScalabilityRoom to scale from clinical batches to commercial supply without a tech transfer.
    Modality ExpertiseProven depth in the specific modality, from small molecule to cell and gene.
    Regulatory & CMC SupportCMC, filing and regulatory support that de-risks the submission.
    Supply Reliability & ResilienceRedundancy, second-source options and a resilient supply chain.
    Technology & Continuous ImprovementModern platforms, continuous manufacturing and data-driven quality.

    Industry trends

    What’s Reshaping the CDMO Landscape in 2026

    The development and manufacturing market is shifting fast, and it shapes which partners biopharma chooses. These are the forces in play, several of them on the agenda at RWE Connect 2026.

    Advanced-Modality Capacity
    Cell, gene and ADC demand outpacing available manufacturing capacity.
    Biologics & Peptide Surge
    GLP-1 and biologics demand driving major capacity investment.
    Supply Resilience & Onshoring
    Reshoring and dual-sourcing to de-risk fragile supply chains.
    Continuous & Digital Manufacturing
    Continuous processing and digital batch records improving quality and speed.
    AI in Process & Quality
    Machine learning optimizing process development and predictive quality.
    Evidence-Informed Lifecycle
    Real-world safety and demand data feeding manufacturing and lifecycle decisions.

    Across the lifecycle

    From Preclinical to Commercial Supply

    CDMOs support a therapy at every stage, and real-world evidence increasingly informs the decisions made along the way.

    1
    Preclinical & FormulationMolecule characterization and early formulation.
    2
    Process DevelopmentScalable, reproducible manufacturing processes.
    3
    Clinical SupplyGMP material for Phase 1 to 3 trials.
    4
    Commercial ManufacturingValidated, at-scale production and release.
    5
    Lifecycle & Post-MarketTech transfer, second-source and ongoing supply.

    The connection

    Why CDMOs Engage with Real-World Evidence

    CDMOs sit upstream of real-world evidence, yet the two are increasingly connected. Here is where the worlds meet, honestly framed.

    01
    Post-Market Safety SignalsReal-world safety and quality data inform manufacturing and corrective-action decisions.
    02
    Demand ForecastingReal-world uptake and adherence data sharpen capacity and supply planning.
    03
    Supporting Sponsor EvidenceSponsors increasingly expect partners fluent in the evidence their products need.
    04
    Outcomes ContextReal-world outcomes shape which modalities and formulations attract investment.
    05
    Regulatory LifecycleRWE now supports label expansions and post-approval commitments partners help fulfil.
    06
    Partnering & GrowthMeeting the RWE, HEOR and biopharma buyers who choose development partners.

    The programme

    What’s on the Agenda

    Two days built around the themes that move real-world evidence forward: the data, the methods, the economics and the decisions it supports. 40+ speakers across keynotes, panels, workshops and the Partnering Lounge.

    Real-World Data & Sources
    EHR, claims, registry, tokenized and genomic data: quality, linkage and access.
    Methods & Study Design
    Study design, causal inference, external controls and regulatory-grade evidence.
    HEOR & Market Access
    Economic models, payer and HTA evidence, and demonstrating value.
    AI & Advanced Analytics
    Machine learning, NLP and generative AI applied to real-world data.
    Regulatory & Policy
    The FDA RWE framework, global reception and evolving evidence standards.
    Partnering & 1:1 Meetings
    The Partnering Lounge: buyers and providers meet by pre-scheduled appointment.

    Formats include keynotes, expert panels, case studies, workshops, the Partnering Lounge and the exhibition. The full session-by-session agenda and speaker line-up are confirmed closer to the event.

    Who is in the room

    Attendee Breakdown

    A senior, focused audience of the buyers who shape development, evidence and partner decisions.

    60%Director / VP and Above
    Director / VP and AboveOther senior roles
    RWE & Real-World Data24%
    HEOR & Market Access20%
    Clinical, Medical & Regulatory18%
    Data Science & Analytics16%
    Development & Manufacturing14%
    Research, Academia & Startups8%

    Seniority is confirmed: 150+ attendees, around 60% at Director or VP level and above. The functional mix shown is indicative; confirmed registration splits are shared with sponsors from the live delegate list.

    Already on board

    Data and Analytics Leaders at RWE Connect 2026

    Truveta
    Magnolia
    Forian
    Arcadia

    Why RWE Connect

    A Generic Pharma Expo vs RWE Connect

    CDMOs spend heavily at vast manufacturing and pharma expos. RWE Connect offers something different: direct access to the RWE, HEOR and biopharma decision-makers who influence partner selection and the evidence behind it.

    A Generic Pharma Expo

    • Enormous halls across every pharma service
    • Evidence and RWE buyers barely present
    • Booths judged on footfall, not conversations
    • Networking left to chance encounters and business cards
    • Limited access to senior decision-makers
    • No view of who is actually attending

    RWE Connect 2026

    • 150+ senior RWE, HEOR and biopharma buyers
    • Around 60% at Director or VP level and above
    • A Partnering Lounge built for pre-scheduled 1:1 meetings
    • Meetings booked with the accounts you name
    • Access to the people who influence partner selection
    • A shared delegate list for warm, targeted follow-up

    Why sponsor

    Meet the Teams Shaping Development and Evidence

    Reach the BuyersRWE, HEOR and biopharma leaders who influence development-partner and evidence decisions, around 60% at Director level and above.
    Pre-Scheduled 1:1 MeetingsName the buyers you want; the Partnering Lounge books the meetings before the doors open.
    Demos and SpeakingPosition your capabilities in front of the sponsors who select development partners.

    What sponsoring looks like

    How a CDMO Wins Business at RWE Connect

    Sponsorship here is built around qualified meetings, not just a stand. This is the typical path from sign-up to signed opportunity.

    Step 1
    Name Your TargetsTell us the sponsors, functions and titles you want to meet.
    Step 2
    Pre-Scheduled 1:1sThe Partnering Lounge books qualified meetings before the doors open.
    Step 3
    Showcase CapabilitiesPresent your modalities, capacity and quality record to decision-makers.
    Step 4
    Speak & LeadKeynote, panel or workshop slots that build credibility.
    Step 5
    Warm Follow-UpLeave with the delegate list and a pipeline of qualified conversations.

    RWE Connect 2026

    Put Your Company in Front of the Room

    150+ real-world evidence buyers, around 60% at Director or VP level and above, over two days in Boston. Request the prospectus and the team replies within one business day.

    • Exhibition space and capability showcases
    • Speaking and panel opportunities
    • Pre-scheduled 1:1 meetings with the buyers you name
    Request the Sponsorship Prospectus
    Three fields. We reply within one business day.

      No public pricing. Enquiry-led, no obligation.

      CDMO Companies: Common Questions

      What are CDMO companies?

      Contract development and manufacturing organizations that develop and manufacture drugs and biologics on behalf of pharmaceutical and biotech companies, across small molecule, biologics and advanced modalities.

      How do CDMOs relate to real-world evidence?

      CDMOs sit upstream of real-world evidence, but increasingly use real-world safety, quality and demand data to inform manufacturing, forecasting and lifecycle decisions, and to support the sponsors whose products generate that evidence.

      What modalities do CDMOs cover?

      Small molecule, biologics, cell and gene therapy, antibody-drug conjugates, sterile fill-finish, and vaccines and plasma products, across every stage from preclinical to commercial supply.

      Which companies are confirmed at RWE Connect 2026?

      Confirmed sponsors to date span data and analytics providers including Truveta, Magnolia, Forian and Arcadia. The programme covers the development, manufacturing and lifecycle themes relevant to CDMOs, with 40+ speakers.

      Why should a CDMO exhibit or sponsor?

      To meet the RWE, HEOR and biopharma decision-makers who influence development-partner selection, and to position alongside the evidence their clients increasingly require. Request the prospectus to discuss options.

      Can my company exhibit or sponsor?

      Yes. Request the prospectus for exhibition, speaking and pre-scheduled 1:1 meeting options; pricing is shared on enquiry.

      When and where is RWE Connect 2026?

      14 to 15 October 2026 at the Hampton Inn by Hilton, Boston Seaport District, Boston, MA.

      What should sponsors look for in a CDMO?

      A clean quality and compliance record, capacity and scalability, proven modality expertise, regulatory and CMC support, supply resilience, and modern manufacturing technology.

      What is the difference between a CDMO and a CRO?

      A CDMO develops and manufactures the product, while a CRO runs the research and clinical trials. Some organizations offer both under one roof.

      How is real-world evidence changing manufacturing decisions?

      Real-world safety, demand and outcomes data increasingly inform capacity planning, demand forecasting, and lifecycle and post-market decisions that manufacturing partners help fulfil.

      How is RWE Connect different from a generic pharma expo?

      RWE Connect gives direct access to senior RWE, HEOR and biopharma buyers through a Partnering Lounge built for pre-scheduled 1:1 meetings, with sponsorship measured in qualified pipeline rather than booth footfall.

      What do CDMO sponsors get at RWE Connect 2026?

      Exhibition space and a capability showcase, speaking and panel opportunities, pre-scheduled 1:1 meetings with the accounts you name, the delegate list for follow-up, and brand exposure to 150+ real-world evidence buyers.

      Join the Movement. Shape the Future.

      Be part of a community that’s redefining how the world measures healthcare impact.

      Join us at RWE Connect 2026
      where data meets decisions.

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