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We are a leading provider of outsourced commercial, medical and recruitment services to pharmaceutical, biotech and healthcare companies. Working exclusively in the United Kingdom, we have brand strategy, implementation, and recruitment experience from numerous launches across prescription medicines, medical devices, and medical software. We provide a UK launch solution for pharmaceutical, biotech and medtech companies, that is an alternative to out-licensing and traditional distribution arrangements.

Pebmond Associates – whether you consider your project or company a Pebble or a Diamond – Our strategic advice and business services for life-science and healthcare organisations adds “Multifaceted Value®”

Strategy, Business Development and Licensing is our focus – whether it is support to acquire, divest or license a product or project -  independent eyes and ears on your company strategy, direction, future plans, project prioritisation or even just general brainstorming – or building your team’s skills in these areas by coaching, face-to-face training, lectures, webinars or e-learning. We do all that - and more importantly, smile at the same time.

Research Donors collects, processes and delivers human blood biospecimens that meet the most demanding research requirements. With a diverse community of  over 2500 donors, we can meet any donor specification as required by your project. Fresh HLA typed human leukopaks, PBMCs, whole blood and blood derivatives, all consented for commercial and genetic research, can be delivered within 24 hours of collection across Europe.

Scendea is a leading product development and regulatory consulting practice serving the pharmaceutical and biotechnology industry. We are committed problem solvers, redefining the meaning of customer service, with a focus on reducing time-to-market and minimising development costs.

Scendea was founded as a result of a management buyout of the product development and regulatory consulting function of a clinical research organisation. Our origin dates back over 20 years, with involvement in over 1,000 development programmes.

Our international team offers strategic and operational support in the fields of quality/CMC, non-clinical/toxicology, clinical/medical and regulatory, which guide products efficiently from early development to marketing approval.

Our scientific excellence, industry experience, commercial awareness and a collaborative approach allow our expert team to solve complex issues associated with medicinal product development.  Scendea has team members based in the UK, Ireland, the Netherlands and the US, who deliver innovative and high-quality solutions aligned to jurisdiction-specific regulatory requirements.

At Scendea we collaborate, innovate, and together with our clients, we succeed.