Scientific Writing

Our experienced team crafts clear, impactful medical and scientific content for:

Pharmaceutical and medical device companies
Regulatory authorities
Universities and research institutions
Educators and healthcare professionals
Patient and public audiences

With over 25 years of experience, there are few scientific outputs we haven’t worked on — from high-impact journal articles to patient education materials.

Medical Device Writing

“Devices are fun… but complex.”
Fifteen years ago, many medical devices could be brought to market with relatively few regulatory requirements. But safety scandals — from collapsing hip implants to leaking breast prostheses — have transformed the landscape.

Today, device documentation must meet rigorous regulatory standards, often approaching the requirements for pharmaceuticals. This includes:

Detailed technical documentation
Marketing materials with robust clinical evidence
Compliance with evolving international regulations

We also support:

In-vitro diagnostics
Hybrid products (device + medicine)
Health apps and digital tools

Our digital division can develop online patient and clinical management tools and guide you through reimbursement processes.

Regulatory Writing

Compliance. Accuracy. Safety.

Meeting regulations, guidelines, and standard operating procedures is essential — not only for regulatory approval, but also to protect patients and ensure product efficacy.

As industry standards tighten and regulatory expectations grow, so does the demand for specialist writers who can:

Produce complex, highly structured documentation
Interpret and analyse data for clarity
Address challenging questions from authorities

Many of our team members thrive on this work — enjoying the structured, detail-driven approach that regulatory writing demands.