Uncover the golden rules for drug development

Put your business on the right track with our seven golden rules to help take your drug product quickly and safely to proof of concept.

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Harness our expertise and capabilities to take your drug development project from the early stages through to clinical manufacturing and beyond

At Recipharm, we’ve been supporting our customers with challenging drug development projects for over 20 years, delivering a wide range of GMP-compliant services from our global facilities.

We understand the complexities of drug development, and our team of highly skilled formulation scientists have the ability to manage your pharmaceutical product development project from preclinical stages up to full-scale commercial manufacturing.

Clinical trial material

Across our clinical trial services, we start with the end in mind to formulate a clear path to getting your drug product to First-In-Human (FIH) studies, later clinical stages, and advancing it to market.

We understand the importance of speed when it comes to reaching important clinical milestones so use our knowledge and problem-solving abilities to overcome hurdles and advance your product to clinic at pace.

Manufactured in accordance with cGMP and in compliance with the US FDA and EU EMA regulations, our services are underpinned by uncompromised high quality standards.

Why choose Recipharm?

Comprised of analytical chemists, organic chemists, formulation scientists, process engineers, manufacturing experts, quality control (QC) and quality assurance (QA) specialists, our experienced team supports you across every stage of the drug development and manufacture process.

With extensive experience in applying GMP across different stages of development and dedicated facilities, we’ll help you overcome your drug development challenges and accelerate the journey to market.