For CDx developers, IVD makers, central labs and regulatory consultancies: pre-scheduled 1:1 meetings with the pharma teams choosing diagnostics partners, at the Boston launch edition in June 2027.
Sponsor Boston 2027
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Trusted by sponsors from our London 2026 launch edition




Our London 2026 sponsors came from five kinds of company, and the Biomarkers & CDx stream adds a sixth. If yours is on this list, the agenda is built around your buyers.
Biomarker testing, flow cytometry and assay services for clinical trials.
Who you meet: Translational medicine and clinical biomarker leads

In vivo models and antibody discovery for immuno-oncology pipelines.
Who you meet: Discovery, pharmacology and preclinical heads
Instruments, reagents and platforms for immune profiling and proteomics.
Who you meet: Immune monitoring and translational science teams

Functional and spatial readouts from patient tissue.
Who you meet: Pathology and biomarker discovery leads
Data, literature and analytics for R&D and competitive intelligence.
Who you meet: R&D strategy and data science teams
The Biomarkers & CDx stream covers CDx development, regulatory strategy and market access.
Who you meet: Pharma CDx, regulatory and medical diagnostics leads
Tell us which roles you need to meet and we will show you how the audience matches up.
Request the prospectusImmunoMark Boston is a companion diagnostics conference in Boston for the companies that pharma teams choose as diagnostics partners: CDx developers, IVD manufacturers, central labs, liquid biopsy companies and regulatory consultancies. The East Coast launch edition runs in June 2027, and its Stream 2 program on Biomarkers & Companion Diagnostics lists “CDx co-development, regulatory pathways, and commercialization” among its key themes.
A CDx sale is a partnering decision, made by several functions and made early. In the US, a companion diagnostic is generally expected to be approved alongside its therapy, so drug developers line up diagnostics partners well before pivotal data. A sponsor’s job is to be in the conversation while the shortlist is still open.
The lab landscape adds a second reason to be there. After a federal court vacated the FDA’s rule on laboratory-developed tests in March 2025, pharma teams are again weighing central-lab approaches against kit-based CDx strategies, program by program. Kit makers and lab service providers both have a case to make to the same buyers, and Boston puts those buyers in one place for two days.
The Boston speaker panel covers the regulatory, diagnostics, pathology and precision medicine functions that sit around a co-development decision. Each one asks a diagnostics partner something different.
| Function on the Boston faculty | What that function weighs in a CDx partner |
|---|---|
| Global Director of Regulatory Affairs (Precision Medicine), Gilead Sciences | Your FDA submission history, bridging study experience and readiness to file alongside the drug |
| Associate Director of Clinical Diagnostics, Regeneron | How your assay moves from clinical trial use to a commercial test, and on what timeline |
| Director, Global Regulatory Affairs, Oncology, AstraZeneca | Whether the diagnostic plan supports the oncology filing strategy in the US and other markets |
| Associate Principal Scientist/Associate Director (R4) – Molecular Pathology, Merck | Scoring reproducibility, tissue requirements and pathologist workflow |
| Scientific Director, Precision Medicine Oncology, AbbVie | Platform fit for the biomarker and the patient selection strategy |
Speakers show which functions are in the room; they are not guaranteed meetings. Your 1:1s come from the full delegate list, so you can reach regulatory, precision medicine and clinical diagnostics roles at every company present. The Boston agenda names companion diagnostics developers, regulatory affairs professionals, CROs and diagnostic labs among the audiences the program is built for.
Stream 2 runs from predictive biomarkers in trials to FDA approvals, value evidence and commercialization. These sessions put your buyers in a partnering frame of mind.
With ctDNA and MRD on both days, this doubles as a liquid biopsy conference in Boston for companies whose tests are moving from monitoring toward patient selection. And because the program spans biomarker evidence, regulation and reimbursement, it works as a precision medicine conference in Boston for teams that sell both assay development and clinical testing. For a current view of the tests your buyers will cite, see our list of FDA-approved companion diagnostics.
Pre-scheduled meetings are the center of a CDx sponsorship. Here is how to plan them for a partnering audience.
Estimate what a set of CDx partnering meetings is worth to your pipeline.
Run the ROI calculatorAt a partnering-led diagnostics conference, the right package is the one that books the most qualified meetings for where you are in the relationship.
Meetings without the overhead, for regulatory consultancies, central labs and CDx business development teams who win work across a table.
For CDx developers and IVD makers with a co-development story to tell on Day 1, ahead of the commercialization panel.
A Day 2 talk on the morning that opens with the FDA oncology approvals keynote and includes health economics.
Package details are on the Boston sponsorship opportunities page, and the exclusive two-stream position is on the Boston headline sponsor page. If your offer is closer to assays and platforms, see the Boston biomarker conference page; for IO services, the Boston immuno-oncology conference page. Comparing editions? The San Diego companion diagnostics conference page covers the February edition, and the London companion diagnostics conference page covers IVDR and MHRA conversations.
Tell us your target functions and we will suggest a meeting package.
Request the prospectusPick a package, add your own numbers and see the pipeline it creates. London 2026 sponsors averaged 15 to 25 meetings each, with 70% senior decision-makers in the room.
1. Choose a package
2. Your numbers
Year-one value of a new pharma or biotech customer
Booth visits, networking and questions after your talk
Share of conversations worth a proposal
Your typical close rate
Sponsorship plus travel and team costs
expected first-year revenue for every $1 of your event budget
Estimates only, based on the numbers you enter. Meetings and inclusions from the Boston 2027 sponsorship prospectus. 1:1 meetings are pre-scheduled with delegates you choose from the attendee list.
We will send your numbers to your inbox, ready to share with your team. Our sponsorship team gets a copy so they can answer questions.
The real London 2026 results, plus profiles of how different types of company use the 1:1 meetings, talks and stand to build pipeline.
What sponsors said
Here is what sponsors told us at our London 2026 launch edition.
We really liked the focus of the event, the topics, the talks, really good opportunity to engage with people, the support we get from you is really great and we appreciate that very much. Based on our experience we would be very interested in also sponsoring the next annual event.

We are always interested in sponsoring interesting conference, based on this years experience, I guess I will manage to get some budget for the next edition.

Conversations I have had are very high level, the footfalls been great and the kind of research going on around is really life changing. We will be very interested in sponsoring the second annual.

My experience here at Immunomark 2026 has been really great. We benefit from very good logistical organisation. Networking sessions were excellent and we consider Immunomark a strategic conference for the coming years.

We got the occasion to discuss customer projects and understand their needs better and how we can help them.

The conference has been great so far with strong interactions at the booth and excellent attendance at our talk. We will definitely think about the next edition.

Quality of the talks were really nice and the attendee list had experts from biotech pharma field. It was great meeting everyone and we look forward to positive outcomes.

The talks have been really interesting so far with a great combination of researchers and clinicians. Moderators encouraged excellent discussions.

Yes. The Boston agenda names CROs and diagnostic labs supporting biomarker assay development, patient stratification and regulatory submissions among its target audiences. Stream 2 covers the whole path from predictive biomarkers in trials to FDA approvals and commercialization, and 1:1 meetings let you reach the teams that decide how trial testing is run.
Day 2 of Stream 2 opens with Keynote: Biomarkers in FDA Oncology Approvals, and Day 1 of Stream 1 includes Translating Biomarker Data for Regulatory/FDA, Predictive and Prognostic Biomarkers in IO trials, and Neoadjuvant and Adjuvant Immunotherapy. The speaker faculty includes Gilead Sciences' Global Director of Regulatory Affairs (Precision Medicine).
Yes. Stream 2 includes Epigenetic Analysis in ctDNA on Day 1 and Biomarkers for Early Detection & MRD on Day 2, so liquid biopsy companies can use the event to reach precision medicine and clinical diagnostics teams.
Yes. The Exclusive 1:1 Meetings packages give 3, 5, 7 or 10 pre-arranged 20-minute meetings with delegate passes, drinks reception passes, the wishlist feature and the delegate list, with no booth or speaking commitment. Speaking slots come with Headline, Platinum, Gold and Silver, each of which includes exhibition space.
Boston (June 2027) is the US East Coast launch edition. San Diego (10–11 February 2027) is the West Coast launch edition. London (3–4 March 2027) is the 2nd annual edition, where European regulation such as IVDR and MHRA is part of the conversation. Packages and the meeting model are the same at every edition.
Tell us who you want to meet. We will send the prospectus and a package recommendation within one working day.