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Life Sciences Marketing Agency: B2B Marketing for Companies That Sell to Pharma, Biotech, Medical Device and CDMO Teams

Updated September 2026 · Written and maintained by the Progression Agency strategy team

Progression Agency is a life sciences marketing agency for companies whose customers work in pharmaceutical, biotech, medical device, diagnostics and contract manufacturing organizations: tools and reagent suppliers, instrument makers, contract research and manufacturing organizations, lab and quality software vendors, and the equipment and facility contractors that build GMP plants. We market to the whole buying group (scientists, process and validation engineers, quality, procurement and executives) from New York City, for clients across the United States and worldwide. Brand and product marketing for drug makers themselves, with medical, legal and regulatory review, is covered on our pharmaceutical marketing page.

On this page · 19 sections
  1. What a life sciences marketing agency does
  2. The life sciences market, segment by segment
  3. The buying group: who decides, and what each person needs
  4. Marketing to R&D labs vs marketing to GMP manufacturing
  5. Claims, labeling and the regulatory lines to respect
  6. How claims review works with our team
  7. Life sciences SEO
  8. Life sciences digital marketing channels
  9. AI search for life sciences suppliers
  10. Content that persuades scientific buyers
  11. Life sciences websites that convert scientific traffic
  12. Life sciences marketing strategy: the first twelve months
  13. Programs by company stage: startups to established suppliers
  14. How to choose a life sciences marketing agency
  15. What life sciences marketing costs
  16. Life science marketing services we provide
  17. Measuring results across a long buying cycle
  18. Why Progression Agency
  19. Related life sciences and healthcare services

The short answerLife sciences marketing works when it respects how scientific and regulated buyers decide: slowly, as a group, and on evidence. The programs that produce qualified demand publish the application data, validation documents and specifications each member of the buying group needs, make them findable in search engines and AI assistants, and keep every claim inside what the labeling and the evidence support. As planning figures from our published pricing guide, a content-led search program runs $2,000–$6,000 a month and LinkedIn Ads management $1,500–$5,000 a month at small-agency rates, with technical or regulated content priced per piece.

Search volumes and costs per click are Ubersuggest data for the United States, pulled 29-30 September 2026. Regulatory references link to the eCFR and FDA. Paul Industries citation data comes from Bing Webmaster Tools for paulindustriesllc.org, a site Progression Agency builds and manages. Price ranges are the small-agency planning ranges published in our marketing agency pricing guide.

How US buyers search for life sciences marketingHow US buyers search for life sciences marketing
Both spellings carry demand; the plural “agencies” searches are shortlists being built.

What a life sciences marketing agency does

Life sciences marketing is B2B marketing to people who work in science and in regulated manufacturing. The products are reagents, instruments, software, services, equipment and outsourced capacity; the customers are research labs, biotech startups, pharmaceutical manufacturers, device makers and the contract organizations that serve them. A life sciences marketing agency turns what the product or service does, and the evidence behind it, into the pages, campaigns and sales material each person in the buying group needs, and measures the result in qualified conversations rather than impressions.

What it is not: advertising prescription drugs to physicians and patients. That work runs under FDA’s prescription drug advertising regulations (21 CFR Part 202) and belongs with a pharma advertising agency. Many life science companies are suppliers to the firms that do it, and their marketing answers to a different audience: the scientist at the bench and the quality lead who must qualify the supplier.

Tools — Reagents and consumables. Search by target and catalog number.
Instruments — Lab automation. Demos and total cost.
CRO — Contract research. Study types and sites.
CDMO — Contract manufacturing. Modalities, scale, inspections.
Device — Medical device. ISO 13485 and QMSR.
GMP build — Equipment and facilities. Process systems, water, cleanrooms.

The life sciences market, segment by segment

The industry writes it both ways, life science and life sciences, and so do buyers: “life science marketing agencies” and “life sciences marketing agency” each draw about 390 US searches a month, and “life sciences marketing agencies” another 320 (Ubersuggest, September 2026). The market behind both spellings is the same, and it splits into segments that sell very differently.

Research tools, reagents and consumables

Catalogs with thousands of SKUs, bought by scientists who search by target, application and catalog number. Product pages need validation data (the application, species and conditions tested), papers that used the product, and a price or a fast quote. Many of these products carry Research Use Only labeling, which shapes what can be claimed.

Lab instruments and automation

Capital purchases with a long evaluation: demos, application notes, total cost of ownership and service coverage. Marketing arms the specialist sales rep with comparison pages, ROI material and webinars run by application scientists.

Contract research organizations

Sponsors choose a CRO on therapeutic experience, study types, sites, timelines and regulatory record. Pages by study type and therapeutic area, with experience figures the CRO is allowed to publish, carry more weight than one general capabilities page.

CDMOs and CMOs

Contract development and manufacturing buyers compare modalities, scales, equipment trains, inspection history and open capacity. A CDMO site that lists its suites, reactor volumes, fill-finish formats and FDA inspection record in text gives sourcing teams the facts that put it on a shortlist.

Bioprocess equipment and GMP facility contractors

Suppliers of process systems, high-purity water, clean utilities, cleanrooms, validation and installation sell to engineering, quality and project teams. This is Paul Industries’ market (see the Paul Industries case study). The search side of that work is on our industrial SEO page.

Medical device OEMs and their suppliers

Device makers buy components, contract manufacturing, sterilization, testing and software under FDA’s Quality Management System Regulation, which since 2 February 2026 incorporates ISO 13485:2016 by reference. Supplier marketing leads with quality system certification, cleanroom classes and design-control support.

Diagnostics

In vitro diagnostic companies sell to clinical labs and health systems, with claims tied to each product’s cleared or approved intended use. Research-only products sold alongside cleared assays need clear separation on the site and in campaigns.

Lab informatics and quality software

LIMS, ELN, QMS and MES vendors sell to IT, quality and operations at the same time. Validation support for electronic records and signatures under 21 CFR Part 11 is often the content that decides the deal.

Biotech platforms and partnering

Early-stage biotechs market to partners, investors and future hires more than to buyers: platform explainers, publications, pipeline pages and a presence at partnering meetings such as the BIO International Convention.

Scientist — Will it work?. Application data.
MSAT — Will it scale?. Scale-up evidence.
QA — Can we qualify it?. Documents and audits.
Procurement — Can we approve it?. Supply and terms.
Regulatory — Will it support a filing?. Master file references.
Finance — Is it worth it?. Total cost.

The buying group: who decides, and what each person needs

A purchase in life sciences usually needs agreement from people who do not share a vocabulary. The scientist cares whether it works in the application; quality cares whether it can be qualified; procurement cares about supply and terms; finance cares about total cost. Content that serves only one of them stalls the deal with the others.

Life sciences buying group: questions, and the content that answers them
RoleTheir questionContent that answers it
Scientist or principal investigatorWill it work in my application?Application notes, validation data, protocols, citing papers
Process development or MSATWill it scale and transfer?Scale-up data, equipment specifications, tech-transfer examples
Quality assurance and validationCan we qualify it and defend it in an audit?Certificates, change-control policy, validation packages, audit history
Procurement and supplier qualityIs the supplier reliable and approvable?Supply continuity, second sources, questionnaires, terms
Regulatory affairsWill it support our filing?Master file references (DMF or device MAF) and regulatory support letters
Executives and financeIs it worth it?Total cost of ownership, risk reduced, time saved

Map content to each role before choosing channels

We list the questions each role asks at each stage, check which ones the current site answers, and fill the gaps in that order. Channels come after, because a campaign that sends a quality lead to a page written for scientists wastes the click.

Give sales the material the buyer’s colleagues need

Much of the buying group never visits the website. Short, shareable documents (a qualification summary for quality, a total-cost sheet for finance) let your champion carry the case inside their company.

Marketing to R&D labs vs marketing to GMP manufacturing

The same company often sells into both worlds, and they behave differently. Research buyers move quickly, value novelty and publications, and often buy on a purchasing card; GMP buyers move slowly, value sameness and documentation, and buy through supplier qualification. Mixing the two messages on one page confuses both.

R&D versus GMP buyers
R&D and discoveryGMP manufacturing
What they valueNew capability, publications, speedConsistency, documentation, security of supply
Evidence that persuadesData in their application, papers citing the productValidation packages, certificates of analysis, audit history
Attitude to changeWelcomeControlled: a change triggers notification and re-qualification
Buying pathThe scientist chooses, often on a purchasing cardSupplier qualification, quality agreement, purchase order
How they searchTargets, methods, catalog numbersStandards, grades (GMP, USP, EP), supplier names
Content that failsGlossy brochures without dataPromises of innovation with no change-control policy
What R&D and GMP buyers weigh (1-5, editorial)What R&D and GMP buyers weigh (1-5, editorial)
The two buyers reward almost opposite things, which is why they need separate pages and calls to action.

When one product serves both

Separate the paths: research-grade and GMP-grade pages, different calls to action (buy or quote, versus request qualification documents), and a plain statement of what changes between grades.

Claims, labeling and the regulatory lines to respect

Life sciences marketing sits closer to regulation than most B2B work. Three sets of rules shape almost every program.

Research Use Only products

In vitro diagnostic products in the research phase must carry the statement “For Research Use Only. Not for use in diagnostic procedures.” under 21 CFR 809.10(c), and FDA’s RUO and IUO guidance addresses products labeled that way but marketed for clinical use. Copy, case studies and ads for RUO products stay in research language.

Claims for cleared or approved products

For cleared or approved devices and diagnostics, marketing claims stay within the cleared or approved intended use. Suppliers that co-market with customers in these categories should expect the customer’s regulatory team to review the material.

Quality and compliance claims

Statements such as “GMP facility”, “ISO 13485 certified” or “ISO Class 7 cleanroom” need the certificate, inspection record or classification report behind them. Buyers ask for it, and a page that links the evidence answers before they do.

Common claims and what substantiates them
ClaimWhat a buyer will ask to see
FDA-registered or FDA-inspected facilityRegistration details, and inspection history from FDA’s Data Dashboard; registration alone does not mean FDA approval
ISO 13485 certifiedA certificate from an accredited certification body, with scope and expiry date
ISO Class 7 cleanroomA classification report to ISO 14644-1, with the test date
cGMP compliantThe regulation that applies (21 CFR 210 and 211, Part 820, or ICH Q7) and the last inspection outcome
USP-grade water or materialsThe monograph or general chapter, and a certificate of analysis
Validated method or systemThe validation report and the protocol it followed
GMP — Named regulation. And the inspection record.
ISO 13485 — Certificate. Scope and expiry.
Class 7 — Cleanroom report. ISO 14644-1.
USP — Monograph. And a CoA.
RUO — Label statement. 21 CFR 809.10(c).
Validated — Report. And its protocol.

Selling to pharma, biotech, device or CDMO teams?Tell us what you sell and who signs off the purchase; we reply with the first three things we would change.

Get a life sciences plan

How claims review works with our team

Every program we run for a life sciences client ships through the client’s own review. We set the workflow up in the first month so that it speeds work up rather than stalling it:

  1. A claims register: every product claim the marketing will make, with the evidence behind it and the reviewer who approved it.
  2. Evidence linked, not described: the certificate, report or paper sits next to the claim on the page where buyers can open it.
  3. Routing by risk: technical copy to your scientist, quality claims to QA, anything touching intended use or labeling to regulatory.
  4. Version control, so a reviewer sees exactly what changed since the last approval.
  5. Re-review on change: a new certificate, a label update or a change notification triggers a check of every page that cites it.

Marketing for life science companies moves faster with this in place, because reviewers approve a known set of claims once instead of rereading every page.

Life sciences SEO

Life sciences SEO is search optimization for scientific and regulated buyers, and it runs on specificity: catalog numbers, targets, methods, standards, grades and regulatory terms. The volumes are small and the intent is high; “life sciences seo” itself draws about 90 US searches a month (Ubersuggest). Most of the traffic that matters arrives on long, precise queries no keyword tool reports. A life sciences SEO agency should be able to show catalog and application pages it has fixed, and the queries they now rank for.

Product and catalog pages

Each product needs a crawlable page with its specifications, applications and validation data in text, Product structured data, and canonical handling for sizes and pack variants. Catalogs generated from an ERP often need template work before content helps.

Application notes and protocols

Application notes and protocols published as HTML pages, with the PDF kept as a download, rank for method searches and get linked from lab wikis, forums and papers.

Publications and citations

Papers that cite a product are the strongest proof a research buyer sees. A citations database searchable by application turns them into pages that rank and persuade at once.

Standards and regulatory terms

Quality and engineering buyers search for the standards and regulations they work under. Pages that explain how a product or service meets them attract the late-stage buyer. Our technical SEO and content marketing teams handle both halves.

Life sciences digital marketing channels

Life sciences digital marketing combines slow organic assets with targeted paid reach, and a life science digital marketing agency earns its fee by knowing which one each segment needs. How the channels line up for a typical B2B life science company:

Life sciences digital marketing channels
ChannelBest forWatch out for
SEO and contentCatalog, method, standard and supplier searchesSlow to build; needs scientific review capacity
AI search optimizationSupplier and method questions put to assistantsMeasurement is young; check monthly
Google AdsHigh-intent product and service searchesSmall volumes; tight match types and negatives
LinkedIn AdsReaching QA, MSAT or procurement roles at named companiesHigh cost per click; needs a strong offer
Scientific publisher and newsletter adsAwareness among researchers in one fieldHard to attribute; negotiate reporting up front
Email nurtureLong cycles and stalled evaluationsList quality and consent
WebinarsApplication education led by scientistsRegistrations are not interest; follow up fast
Trade showsRelationships and demos: BIO, SLAS, INTERPHEX, CPHICostly; plan the pre-show and post-show digital work

Account-based programs for named accounts

Where the universe of buyers is a few hundred companies (a CDMO selling to clinical-stage biotechs, for example), account-based programs target named accounts across LinkedIn, email and display, with content for each account’s modality and stage.

Product and service searches in life sciences are often too small for broad campaigns. Exact terms, catalog numbers and competitor comparisons with strict negatives keep Google Ads spend on buyers.

How a life sciences purchase movesHow a life sciences purchase moves
Qualification is the step B2B marketing most often forgets to support.

AI search for life sciences suppliers

Scientists and engineers now ask assistants to shortlist suppliers and explain methods. Being cited depends on pages that answer those questions directly, and on the crawlers being allowed in. Our AEO for pharma and life sciences page covers that program in detail.

Data from one supplier in this market: Paul Industries, which provides process equipment and high-purity water systems to pharmaceutical and biotech plants, holds 43% of Copilot and Bing AI citations on one documentation question and 40% on one provider-selection question (Bing Webmaster Tools, September 2026), and ChatGPT names it in 8 of the 10 supplier-selection questions tracked for it (Ubersuggest, September 2026; see the Paul Industries case study). These are questions a buyer asks before choosing a supplier.

Answer-first pages

Open with the direct answer (what the method is, which grade meets which standard, what a qualification package contains), then give the detail and the evidence.

Consistent company facts

Company name, sites, certifications and product names should match across the website, directories and partner listings, so an assistant can connect them to one supplier.

Crawler access

Confirm that robots rules and bot protection allow the crawlers behind Copilot, ChatGPT, Perplexity and Google.

Content that persuades scientific buyers

Scientific buyers discount adjectives and reward data. Content by stage of the evaluation, with the person inside your company who owns the facts:

Life sciences content by funnel stage
StageContentWho owns the facts
Problem recognitionMethod explainers, standards guides, webinarsApplication scientists
Solution explorationApplication notes, comparison pages, calculatorsProduct management
EvaluationValidation data, protocols, demo or sample programsField application scientists
QualificationCertificates, quality agreements, change-control policy, audit supportQuality assurance
PurchasePricing or quote paths, supply terms, lead timesSales operations
Adoption and expansionTraining, protocols, user publications, new applicationsCustomer success

Case studies when clients cannot be named

Life sciences clients often cannot be named. Anonymized case studies that keep the modality, scale, problem and measured outcome still persuade; invented ones do lasting damage when a buyer checks.

Scientist-led webinars

A webinar presented by an application scientist, with a real data set, draws researchers. The recording becomes a page, a set of clips and an email sequence.

Calculators and tools

Tools engineers and scientists reuse (dilution and buffer preparation, flow velocity, dead-leg ratio, cleanroom air changes) earn repeat visits and links.

Explainers — Awareness. Methods and standards.
App notes — Exploration. Data in context.
Protocols — Evaluation. Reproducible steps.
Packages — Qualification. Certificates and policies.
Quotes — Purchase. Fast and complete.
Training — Adoption. And new applications.

Life sciences websites that convert scientific traffic

A life sciences website has to work for a scientist hunting a catalog number, a quality lead looking for a certificate and a sourcing manager checking capacity, often on the same afternoon.

Search and product finders

Site search that understands catalog numbers, targets and synonyms, and product finders filtered by application, species, format and grade.

Documents on demand

Certificate of analysis and safety data sheet lookup by lot number, and qualification packages behind a short request form rather than a sales call.

Quote and sample paths

Quote carts for configured products, sample and demo requests that route to the right field scientist, and distributor lookup by country for international buyers. Our web team builds these; see B2B website design for the wider approach.

Life sciences marketing strategy: the first twelve months

A life sciences marketing strategy starts from the buying group and the evidence you can publish, not from channels. The sequence we use for an established supplier:

The first twelve months of a life sciences marketing programThe first twelve months of a life sciences marketing program
Claims review is set up in month two so that every later page ships through it.

A life science marketing strategy for a platform biotech runs differently: partnering and investor audiences first, then the scientific community, with publications and conference presence as the main channels and the website as the reference point.

Programs by company stage: startups to established suppliers

Pre-revenue biotech platforms

Audience: partners, investors and future hires. Assets: a platform explainer, pipeline and publications pages, and the team. Channels: partnering meetings, LinkedIn and press.

Tools and reagent companies scaling up

Audience: researchers in defined applications. Assets: product pages with validation data, citations and protocols. Channels: SEO, Google Ads on catalog terms, email and webinars.

Established CDMOs and CROs

Audience: sourcing, program management and quality. Assets: capability pages by modality and scale, inspection history and capacity. Channels: account-based programs, LinkedIn, conferences and AI search.

International suppliers entering the US

Audience: US buyers who need to know about supply chain, local support and regulatory standing. Assets: US-facing pages with US units and standards (USP alongside EP) and distributor and service coverage. See international SEO.

How to choose a life sciences marketing agency

Lists of the best life science marketing agencies are a starting point. The answers to the questions below are what separate them, and the same questions apply to a life sciences marketing consultant, a small life science marketing consulting practice or a larger life science marketing firm: the difference between them is capacity, not standards.

Questions to ask a life science marketing firm
QuestionA strong answerA warning sign
Who writes our scientific content?Writers who can read the science, reviewed by your expertsGeneralist copywriters and no review step
How do you handle claims review?A documented workflow with your regulatory and quality teams“We keep it high level”
Which segments have you marketed to?Named modalities, instruments or services, with examples“All of healthcare”
How will you measure success?Qualified meetings, opportunities and pipeline by sourceImpressions and followers
What happens to our assets if we part ways?You own the site, content, data and ad accountsAssets held in the agency’s accounts
How do you use AI in content production?Drafting under expert review, with every fact checkedUnreviewed AI output

Life science marketing companies that answer those six well are rare enough that the shortlist usually writes itself. A life sciences marketing company that cannot answer them is not ready for your review process, however polished its portfolio.

Need content your scientists will approve?We write from interviews with your experts and route every claim through your review before it goes live.

Talk to us

What life sciences marketing costs

Our published planning ranges apply to life sciences work (small-agency column of the marketing agency pricing guide): a content-led search program at $2,000–$6,000 a month, LinkedIn Ads management at $1,500–$5,000 a month, email marketing management at $500–$4,000 a month and a marketing automation retainer at $1,500–$8,000 a month. Technical or regulated content runs $2,000–$8,000 a piece at agency rates, a white paper $5,000–$20,000 and an interview-based case study $1,200–$4,000. Trade show presence, including booth, staff, collateral and follow-up, runs $8,000–$120,000 a show.

Media spend sits on top of management fees. For a sense of what search traffic costs in this market, here is what advertisers bid for the phrases buyers use to find agencies like ours:

What advertisers bid for life sciences agency searchesWhat advertisers bid for life sciences agency searches
Device and life sciences agency phrases carry the highest bids in this set.

Life science marketing services we provide

Our life sciences marketing services, delivered by one team from the same buying-group map:

  • Positioning and messaging for each member of the buying group, reviewed by your scientists.
  • Life sciences SEO: product and catalog pages, application content and technical fixes.
  • AI search optimization for supplier and method questions.
  • Website design and development for catalogs, CDMO capability sites and instrument launches.
  • Google Ads and LinkedIn Ads programs with account-based targeting: the work of a life sciences advertising agency, planned from the same map.
  • Email nurture and marketing automation connected to your CRM.
  • Application notes, white papers and case studies written from interviews with your experts.
  • Webinar programs and trade show campaigns, before and after the event.
  • A claims review workflow built with your regulatory and quality teams.
  • Reporting in qualified meetings, opportunities and pipeline by source.

Measuring results across a long buying cycle

Long cycles make last-click reporting misleading. We track the leading signals that each stage of the buying group produces, and reconcile them against opportunities in the CRM every month.

Leading indicators

Sample and demo requests, certificate and data sheet downloads, application-note reads and webinar attendance, segmented by account where the CRM allows.

Pipeline indicators

Qualified meetings, opportunities created and opportunities advanced, by source and by segment.

Visibility indicators

Rankings for product and method terms, and citations in AI answers checked on a fixed monthly schedule.

Meetings — Qualified. The first outcome.
Samples — Requested. By product.
Downloads — CoA and SDS. Intent signals.
Pipeline — By source. From the CRM.
Citations — In AI answers. Checked monthly.
Cycle — Length. Tracked by segment.

Why Progression Agency

We are a full-service search, content and paid media agency based in New York City. Working as a life science marketing agency inside that structure means one team for the website, search, AI answers and paid campaigns, working from evidence your scientists and quality team can stand behind. Our work in the regulated supply chain includes Paul Industries, which provides process equipment and high-purity water systems to pharmaceutical and biotech plants and whose site Copilot now cites around 200 times a day; the Paul Industries case study has the detail.

Planning life sciences marketing?

Tell us what you sell, to which segment and who signs off the purchase; we reply with a written plan and a fixed scope.

Get a life sciences marketing proposal

By industry and by situation

Frequently asked questions

What is life sciences marketing, and what does an agency do?
Life sciences marketing is B2B marketing to scientific and regulated buyers. An agency markets products and services to scientific and regulated buyers: researchers, process and validation engineers, quality, procurement and executives in pharma, biotech, device, diagnostics and contract organizations. The work spans positioning, website, search, AI answers, paid media, content and events, measured in qualified pipeline.
Is it life science marketing or life sciences marketing?
Both are used for the same market. Buyers search both ways in roughly equal numbers: “life science marketing agencies” and “life sciences marketing agency” each draw about 390 US searches a month (Ubersuggest, September 2026).
How is life sciences marketing different from pharmaceutical advertising?
Pharmaceutical advertising promotes prescription drugs to clinicians and patients under FDA’s advertising rules. Life sciences marketing is mostly B2B: selling tools, services, equipment and capacity to the companies and labs that research, develop and make those products.
Which life sciences companies do you work with?
Suppliers across the value chain: research tools and reagents, instruments, CROs and CDMOs, lab and quality software, device suppliers, and the equipment and facility suppliers that build GMP plants, such as Paul Industries.
How do you market Research Use Only products without making clinical claims?
By keeping all copy, case studies and ads in research language, carrying the RUO statement required by 21 CFR 809.10(c), avoiding diagnostic performance claims, and routing borderline material through your regulatory team before it runs.
Can you write content our scientists will sign off?
Yes. We interview your scientists and engineers, write from their words and data, and send every page through their review. Nothing technical publishes without an expert’s approval.
Why do life sciences sales cycles run so long, and what can marketing do about it?
Several people must agree, and GMP buyers must qualify a supplier before buying. Marketing shortens the wait by publishing what each member of the buying group needs to say yes, from validation data to qualification packages, so fewer questions wait for a meeting.
What does life sciences SEO involve?
Crawlable product and catalog pages with specifications and validation data, application notes and protocols in HTML, citation pages, standards explainers, structured data and technical fixes, all aimed at the precise queries scientists and quality buyers use.
Do life sciences companies need AI search optimization?
Increasingly, yes. Engineers and scientists ask assistants to shortlist suppliers and explain methods. Paul Industries, a supplier to pharma and biotech plants, holds 43% of Copilot and Bing AI citations on one documentation question (Bing Webmaster Tools), and ChatGPT names it in 8 of the 10 supplier-selection questions tracked for it (Ubersuggest).
What does a life sciences marketing program cost?
From our published small-agency ranges: $2,000–$6,000 a month for a content-led search program, $1,500–$5,000 a month for LinkedIn Ads management, and $2,000–$8,000 per piece for technical or regulated content. Media spend and trade shows are extra.
Should a CDMO publish its FDA inspection history?
The history is already public on FDA’s Data Dashboard, so buyers can find it anyway. Publishing it with context, including what changed after any observations, answers the sourcing team’s question and shows confidence.
What makes a good life sciences case study when clients cannot be named?
Keep the modality, scale, problem, approach and measured result, remove the identifiers, and get the client’s approval for the anonymized version. Never invent or composite a case.
Do you run LinkedIn Ads for life sciences companies?
Yes, targeting by job function, seniority and named accounts, with offers matched to each role: data for scientists, qualification material for quality, cost models for finance.
Which trade shows matter for life sciences marketing?
It depends on the segment: BIO International Convention for partnering, SLAS for lab automation, INTERPHEX for pharmaceutical manufacturing technology, CPHI for pharmaceutical ingredients and services. We plan the digital work before and after each show.
Can you market medical device components and services?
Yes. Supplier marketing to device makers leads with quality system certification, cleanroom and process capabilities and design-control support, and follows FDA’s Quality Management System Regulation, in force since February 2026.
Which features does a life sciences website need that an ordinary B2B site does not?
Search that understands catalog numbers and targets, product pages with validation data, application notes, certificate and data sheet lookup, qualification packages on request, quote and sample paths, and facts a supplier-qualification form asks for.
Which numbers show whether life sciences marketing is working?
Leading indicators (sample requests, document downloads, webinar attendance), pipeline indicators (qualified meetings and opportunities by source) and visibility indicators (rankings and AI citations), reconciled against the CRM monthly.
Can you market a European or Asian life sciences supplier to US buyers?
Yes. We work worldwide and help international suppliers enter the US market with US-facing pages, US units and standards alongside EP or JP references, and distributor and service coverage.
Can you work alongside our in-house marketing and scientific teams?
Yes, and most of our life sciences work runs that way. Your team keeps ownership of positioning and approvals; we add the writing, web, search and paid media capacity, and plug into your existing review workflow rather than inventing a parallel one.
What should we prepare before a life sciences kickoff?
A short list of products or services and segments, access to analytics and the CRM, two or three hours with a scientist and a quality lead for interviews, and your claims review contacts.

Selling to pharma, biotech, device or CDMO teams?Tell us what you sell and who signs off the purchase; we reply with the first three things we would change.

Get a life sciences plan

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