Pharmaceutical consultancy services for market access, medical writing and pharma workshops

Facilipharma provides specialist pharmaceutical consultancy services for pharma, biotech and healthcare organisations, including market access consultancy, early market insights, medical writing and facilitated pharma workshops.

Pharma Workshops

Facilipharma delivers specialist facilitation and workshop support services, specifically tailored to businesses and organisations within the pharmaceutical industry.

Medical Writing

Facilipharma offers premium medical writing services focused on Market Access and Regulatory needs. With personalised, high-quality design and innovative content, we deliver value.

Early Market Insights

Facilipharma empowers early-stage teams with strategic insight into commercial potential, pricing, and market access. Our early market insights help shape smarter trial designs, inform investor pitches, and accelerate product development.

Market Access Consultancy

Facilipharma supports pharmaceutical companies in bringing products to market with tailored strategies, payer-informed communication, and global value dossiers. Our consultancy combines evidence, insight, and creativity to unlock access.

Looking for something specific? Our experience in Pharma allows us to create bespoke services and packages for our clients. Get in touch to share your needs.

marie cut out 1

Meet The Founder

Meet Marie Chivers, the Founder of Facilipharma. With a wealth of experience in pharmaceuticals, holding both an MPharm and a PhD in Pharma, Marie is passionate about driving innovation and progress in the industry.

20+ Years

Pharmaceutical industry experience

MPharm

Master of Pharmacy

PhD Pharma

Doctorate in Pharmaceutical Sciences

IAF Member

International Association of Facilitators

Reviews

Partner
Global Pricing and Market Access Consultancy
Marie played a crucial role in supporting us through a fast-paced project with multiple workstreams, demonstrating exceptional organization and proactiveness. Thanks to her leadership, we successfully met the client’s tight deadlines, receiving high praise for both the quality of the final deliverable and the engagement throughout the project. I look forward to working with Marie again on future projects.
EU Market Access Lead
Global Pharmaceutical
It was a pleasure working with Facilipharma. Marie Chivers took the time to understand what we needed and how we could achieve this in a pragmatic way. The deliverable then followed easily and on time!

FAQs

Facilipharma offers an integrated range of pharmaceutical consulting and communication services that support your product from early development to market launch and beyond. We work with start-ups, biotechs, global pharma companies, and investment teams across all stages of the product lifecycle.

Our four core services include:

Explore our full services overview for more detail.

Market access can make or break a product. At Facilipharma, we help pharmaceutical teams prepare for successful reimbursement by combining strategy, evidence, and messaging.

Our Market Access Consultancy service includes:

Service AreaWhat We Deliver
Global & Local Value DossiersCustomised content for HTA submissions across the UK, EU, and US
AMCP & JCA DossiersTailored documents aligned to payer/regulatory body expectations
Objection Handling StrategyAnticipation and response to likely payer questions during review
Payer Testing & Insight GatheringDesk research and primary interviews to validate messaging
Stakeholder MappingIdentification of reimbursement decision-makers by market

We don’t just write submissions, we help you craft a compelling value story that connects the clinical and economic evidence to what really matters to decision-makers.

For a closer look, visit our Market Access page.

Our Medical Writing Services cover both technical regulatory content and high-impact value communications. We bring together clinical accuracy, visual clarity, and strategic storytelling.

Here’s a breakdown of what we support:

Regulatory Medical Writing

  • Clinical Study Reports (CSRs)
  • Investigator Brochures
  • JCA Dossiers
  • Regulatory Briefing Documents

Market Access Writing

  • HTA Submission Documents
  • AMCP Dossiers (for US Market)
  • Global/Core Value Dossiers
  • Payer Value Slide Decks

Scientific Communications

  • Journal Manuscripts
  • Posters and Presentations
  • White Papers and Expert Consensus
  • Plain Language Summaries

Digital & Visual Content

  • Scientific animations
  • Digital explainer slides
  • Payer-optimised infographics

We also ensure that all materials are designed with usability in mind, whether your reader is a regulator, payer, or physician. Learn more on our Medical Writing page.

Too often, commercial strategy is treated as a late-stage consideration. At Facilipharma, we believe it’s never too early to understand the market potential of your innovation.

Early Market Insights can:

  • Reveal pricing potential and likely reimbursement hurdles
  • Inform clinical trial endpoints and comparator choices
  • Identify payer concerns early — before protocol lock
  • Improve investor confidence and pitch alignment
  • Enable strategic pivots that maximise long-term value

We support early-stage innovators with desk research, HTA reviews, payer insights, and opportunity appraisals, so you’re not making decisions in the dark.

This type of support is especially valuable for:

  • Biotech spinouts
  • Seed/Series A fundraising
  • Preclinical and Phase I/II product planning

Visit our Early Market Insights page to see how we can help shape smarter development from day one.

Our Pharma Workshops are designed for real outcomes, not just discussions. We work with cross-functional teams across clinical, regulatory, manufacturing, commercial, and executive leadership to unlock decisions and solve challenges.

Popular workshop themes include:

Market Access Strategy

  • Value messaging development
  • Objection handling training
  • Payer alignment sessions

Manufacturing & Quality

  • FMEA Risk Assessments
  • Root Cause Analysis (RCA)
  • Deviation Investigations

Early Development

  • Target Product Profile (TPP) creation
  • Clinical trial design and endpoint selection
  • Early commercial planning

Communication & Collaboration

  • Group working methodology training
  • Presentation and meeting skills
  • Cross-functional leadership alignment

Facilipharma’s founder, Marie Chivers, is also a trained IAF facilitator, blending technical fluency with communication expertise to help teams move forward productively.

We’re small and that’s by design.

Working with Facilipharma means you get direct access to senior expertise, not junior teams hidden behind layers of account management. Here’s why our clients trust us:

  • Experience – 20+ years in pharma, including HTA, regulatory, and product development
  • Agility – Fast, flexible, and responsive to your timeline and team structure
  • Customisation – Every project is designed around your goals, not templates
  • Continuity – Work with the same core consultants throughout your project
  • Holistic Support – Strategy + Writing + Insight + Facilitation = one joined-up solution

We’re not here to take over, we’re here to amplify your team’s capabilities.

You can learn more about Marie’s background and ethos on our About page.

You can contact us directly via our contact page, or reach out by phone or email:

Whether you’re ready to begin a specific project or just want to explore how we can help, we’re always happy to book an introductory call and discuss your needs.

We also offer bespoke service packages depending on your product stage, team structure, and timeline.

Contact Us

Have you got a question or enquiry? Get in touch.

Get In Touch

To learn more about our pharmaceutical workshops, market opportunity analysis, medical writing or anything else, you can send us a message via the contact form.

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