SpectrumX Medical, an exciting new pharmaceutical company are in the process of entering the UK and European Healthcare markets, with their associated proprietary formulations of HOCl (Hypochlorous Acid).

Integrated Life Science Group Ltd are delighted to have been selected as SpectrumX Medical’s exclusive Project Partner responsible for ensuring compliance and development through the various stages of entering the UK and EU markets. We will be developing strategies to ensure smooth transactions through a number of clinical trials, and the drug development of their products – we will also be supporting with fitout and qualification of a state-of-the-art fill finish facility in the UK.


Key Personnel

Derek Brown

A highly professional and entrepreneurial pharmaceutical consultant with over 30 years of UK and EU Pharmaceutical Market experience. Former Hospital Director at the UK’s largest Generics company with broad experience across Biosimilars, Proprietary and Generic products. Former Board member of the British Generics Manufacturers Association (BGMA), current member of the BGMA Secondary Care Group, and member of the NHS Partnership Group. Member of the British Biosimilars Association. Extensive knowledge of the pharmaceutical supply chain with focussed expertise in executing product launch strategies. A strategic thinker with excellent interpersonal skills who has managed several very successful Key Account Management teams. Specialist expertise in tendering/contracting with the NHS in all four home nations and was intrinsic in transforming his former company’s underperforming hospital business unit to be one of the top suppliers to the NHS.

Temi Giwa

Temi is an experienced clinical research professional consultant with over 20 years in operational trial management, working within diverse business models such as start-ups, academia, biotech, pharmaceuticals, and clinical research organisations. With an extensive experience of managing multi-therapeutic and multi-phase (first-in-man to post marketing) projects across multi-regions, speciality areas include clinical trial compliance leading on regulatory inspections (European EMEA and US FDA) and rescue project management.

Leah Heathman

A senior Regulatory Affairs professional with 15 years’ experience across a broad range of therapeutic areas within leading pharmaceutical companies. Extensive knowledge of regulatory procedures ensuring successful registration and maintenance within the EU and RoW. A strong leader competent in line-management, ensuring productive and happy teams and experienced in setting up Regulatory systems/processes, writing SOPs and training. An effective communicator delivering regulatory strategy and engaging with cross-functional teams and global Health Authorities. A Green Belt in Lean Six Sigma with proven project management skills and a drive for achieving project objectives with a clear focus on compliance and commercial timelines.