We are a life science consultancy helping biotech, pharma, and medtech teams navigate global regulations and deliver evidence-led documentation that gets innovations to patients.
Whether you are preparing an IND, aligning to EMA expectations, planning your HEOR toolkit, or raising a Series A – we bring the experience, speed, and strategy to get you there.
We support clients with:
Senior experts lead and deliver our work, no bloated teams and no junior handoffs.
Just fast, credible, compliant deliverables, designed to land first time.
We combine deep regulatory expertise, medical clarity, strategic storytelling, and real-world patient insight to support the full journey – from preclinical development to market access, fundraising, and global launch.
We bring big pharma quality with specialist speed – helping biotech, pharma, and medtech teams move faster, without compromising compliance or credibility.
As a specialist life science consultancy, our team combines senior regulatory writers, scientific strategists, medical experts, and investor-ready storytellers. Every deliverable is grounded in evidence, shaped by experience, and focused on outcomes that matter.
We don’t just understand your science. We know how to position it – to regulators, payers, clinicians, and capital partners alike.
We are not a legacy medcomms agency or generalist shop. We are lean, senior, and focused on outcomes that move your business forward.