Pharma Marketing Agency
You’re not looking for a “partner.” You’re looking for someone who gets the job done—correctly, legally, and in ways you can measure.
We understand pharma. We know how hard it is to gain traction with prescribers, MSLs, procurement teams, and decision-makers when your message is tangled in regulatory red tape, your ad budgets are being scrutinized, and your competitors are throwing out feel-good brand campaigns without real value.
That’s why we built our pharma marketing service to do one thing better than anyone else: get qualified attention that turns into action.
Our Services
Each of these is created for one purpose: ensuring the right people hear your message—and care enough to respond.
Regulatory-Compliant Paid Search (PPC & Programmatic)
Your audience doesn’t click ads randomly. In pharma, they search for treatment alternatives, clinical guidance, peer-reviewed insights, and brand names. We build and manage media campaigns that follow FDA and MHRA rules while still attracting high-intent traffic.
How it solves your issue:
- Instant visibility to prescribers actively searching
- Custom-built negative keyword maps to reduce brand safety risks
- Retargeting segments based on behavior groups (HCP, academic, C-suite pharma buyers)
- Review pathways pre-approved with med-legal teams for efficient ad copy.
Expected outcome:
Reduce Cost per Acquisition by 18–22% through accurate bidding and intent filtering.
KOL and HCP Outreach Funnels
Pharma reps can’t get past the front desk. Emails get ignored. LinkedIn DMs disappear. We deploy compliance-safe outreach through automated workflows, segmented contact lists (NPI & DEA verified), and custom-built landing pages for HCP onboarding.
How it solves your issue:
- Increases open rates via large-scale personalization
- Ensures GxP, HIPAA-safe handling of sensitive interaction data
- Sequence timing aligns with the clinical trial phase and the drug lifecycle stage.
- Interaction is tracked using CRM-based lead scoring.
Outcome:
3X interaction increases within Tier 1 specialist groups in oncology, neurology, and rare disease.
Medical SEO – Intent-Mapped and Index-Rich
This isn’t generic blog content. We write search-focused medical material based on actual patient questions, peer-reviewed sources, and FDA terminology. Structured schema markup, page tagging, and topic clustering help us appear where decision-makers look.
How it solves your issue:
- Attracts prescribers researching clinical data or treatment comparisons
- Builds awareness in early phases via search result visibility
- Cuts down on ad reliance over time with lasting, high-authority content
Expected outcome:
53% increase in organic visibility within 4–6 months for branded and non-branded queries.
Pharma-Safe CRO (Conversion Rate Refinement)
Your landing pages are likely under-delivering. Why? Because pharma pages can’t use urgency tactics, pricing nudges, or aggressive prompts. We build conversion paths based on trust elements, compliance-safe UX, and data gatekeeping.
How it solves your issue:
- Improves HCP sign-up rates using NPI verification + token onboarding
- Applies signals of expertise, credibility, and reliability to reduce bounce
- A/B testing using industry-specific benchmarks in pharma and biotech
Expected outcome:
Average 29% increase in contact form completions across branded campaigns.
Compliance-Cleared Email Campaigns
Whether you’re handling MSL support, investigator outreach, or payer communications, pharma emails can’t look like sales copy. We develop segmented email flows that comply with legal teams while increasing engagement with relevant content.
How it solves your issue:
- Timing based on provider availability from open-source data
- Uses compendium data to build personalized logic
- Manages opt-outs under CAN-SPAM and GDPR guidelines
Expected outcome:
Consistent 15–21% open rates and 8–10% click-through rates for non-branded, HCP-directed emails.
Product Launch Positioning and Messaging
We don’t just bring brands to market—we guide your team through talking to different groups at every approval stage. Using category context, mechanism-informed messaging, and unbranded copy that meets access rules, we help pre- and post-launch messages hit with clarity.
How it solves your issue:
- Distinguishes your product in saturated categories
- Adjusts communication by stage: pre-approval, NDA submitted, market-ready
- Matches language with what med-legal teams will approve
Expected outcome:
Faster prescriber awareness and formulary discussion within 60–90 days post-launch.
Pharma-Focused Web Design and Development
Made for compliance, speed, and simplicity. Whether you need a branded content hub or a modular, unbranded resource, we build fast-loading, clean-code websites with schema markup ready for HCP, KOL, or patient targeting.
How it solves your issue:
- Stops bounce from poor mobile experience
- Fully meets ADA, WCAG, and FDA content rules.
- Easily adapted for region-specific regulatory requirements.
Expected outcome:
+34% increase in mobile session duration in APAC and North America.
Media Planning + Placement for Pharma
We don’t just “buy media.” We create integrated systems that match the long decision timelines of pharma. That includes medical journal placements, peer education spots, programmatic display, and healthcare podcast sponsorships.
How it solves your issue:
- Chooses channel and budget by audience behavior segments
- Ties each media type to both clinical and business outcomes
- No waste on unmeasured placements or vanity metrics
Expected outcome:
Lower cost-per-thousand impressions in niche pharma channels, and 2.4x increase in page time vs. general placements.
Why Choose Us?
We’re not generalists. We’re from pharma commercialization, clinical launch teams, and regulated medical messaging. We’ve created launch kits for EMA, dealt with med-legal conflicts, and written compliant copy that passed procurement and FDA review.
We’ve worked with brands that had one chance to enter a crowded field—and made that chance count.
Here’s the truth: Pharma isn’t just complex. It’s demanding. And we’re built to handle that pressure.
Technical FAQs
Yes. All paid and organic messaging follows OPDP guidance. We submit annotated review packets with supporting references and past approvals.
We use consent-first workflows with hashed IDs and verified contact methods, approved through DPO review.
Yes. Our frameworks adapt per phase (I–IV), shifting tone and claims as required by regulations.
We apply multi-touch tracking and CRM mapping, scoring HCP activity based on specific milestones (sample requests, formulary inclusion, etc.)
Yes. We focus on condition-based and educational campaigns that meet FDA and EMA unbranded standards.
Yes. Our data systems work with Salesforce, Veeva, HubSpot Health, and Medidata for smooth integration.
Usually 2–4 weeks, depending on internal med-legal processes and review steps.
Ready to See Real Outcomes?
Let’s stop draining your budget on vague impressions and start building marketing that shows up in the numbers. We know pharma, we write for pharma, and we help you grow without crossing any compliance lines.
Book Your Call – Let’s Talk Measurable Results
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