We are regulatory affairs and market access consultants

We are based in London UK, and help small, and medium-sized healthcare businesses with innovative solutions reach patients in overseas markets through a guided and facilitated process.

What we do

We provide bespoke guidance and consultancy services on regulatory affairs and market access which enables a fast and cost-effective entry of your therapy to an overseas market. We guide you walk through a local regulatory environment without letting you alone
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How we do

Providing information on a different regulatory environment should be informative enough until the launch of your business; therefore we work closely with you from the start until the end providing all necessary and complementary services, so you launch your business as quick as possible.
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The Result

A complete regulatory and market access toolkit that includes guidance, strategy, intelligence, documentation, submission and follow up to launch your business and therapies successfully helping other patients. We can show all stakeholders the value of your product as you define it.
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What we do

Regulatory Affairs & Market Access

We specialise in marketing authorisation approval of pharmaceuticals and a variety of health care products including cosmetics and medical devices. Tailored to market access of your products starting from regulatory planning.

What we offer and excel at providing

• Delivering a bespoke regulatory and solutions tailored to your products
• Consultants with many years’ experience in regulatory affairs and market access
• Open communication throughout the process and timely feedback
• Focused on achieving the results you need to grow or launch your business
• Compiling documentation in eCTD format and adaptation to local requirements
• Local adaptation of your global pharmacoeconomics model for local HTA requirements

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What Our Clients Say

Let’s Work Together

Like what our clients say, and interested in working together? Get in touch so we can discuss your requirements.