Oncimmune

Oncimmune, a global leader in immunodiagnostics and (auto) antibody biomarker profiling & discovery in immuno-oncology, autoimmune and infectious diseases. Through its ImmunoINSIGHTS™ technology platform, the company provides insights to discover and validate novel biomarkers, improve treatment responses and adverse event (irAE) prediction, patient screening and diagnostic accuracy.

Oncimmune is headquartered in the UK with operations in Germany and USA.

Company type
Keywords
oncology
Dr Mike Fisher
LinkedIn logo Vice President, Head of Business Development 

PharmaVentures

Company type
Jessie You
Director 
Dr Kate Moore
Vice President 
Ralph Hughes
Vice President 

PrecisionLife

PrecisionLife is an innovative techbio changing the way the world looks at predicting, preventing, and treating chronic diseases - extending the reach of precision medicine beyond cancer and rare disease for conditions that account for over 80% of healthcare spending. We stratify patient populations at an unprecedented level of resolution to reveal the deepest disease insights in complex, chronic conditions. Our scalable platform is generating a growing IP portfolio of novel drug targets, drug response biomarkers, and precision repositioning assets for over 45 indications. All our assets are protected by our unique and highly specific patient stratification biomarkers, with an understanding of disease prevalence, efficacy and secondary indication potential to maximize their probability of success in clinical development. Our unparalleled understanding of disease biology and patient stratification informs and derisks every stage of drug discovery and development, giving major competitive advantages and creating additional revenue opportunities for our biopharma partners. Recent deals offer significant commercial validation to our approach:
  • Multi-target R&D Partnership: Strategic R&D partnership with Ono Pharmaceutical to discover and validate multiple novel therapeutic targets in CNS, signed in Dec'22
  • Precision Neuroscience Partnership: Collaboration with Sosei Heptares for deeper evaluation of one of their GPCR targets, signed in Nov'22
At Bio-Europe, we are prioritizing meetings with companies interested in partnering around a range of complex chronic disorders, including CNS, respiratory, immunological and cardiometabolic indications, and those seeking partnerships around novel targets, precision drug repositioning, clinical trial analysis and patient stratification biomarkers in complex chronic disorders.
Company type
Dr Georgia Gliki
LinkedIn logo Vice President Business Development 
Gianluca Valenza
LinkedIn logo Business Development Director 

Present Value

Company type
Andrew Dean
Director 
James MacDonald
Associate Director 

ProImmune

Website:
proimmune.com
Company type
Charlotte Thompson
Immunology Sales Specialist 

Research Donors

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. 

Research Donors only provides samples that have been collected under the most stringent levels of ethics and consent. All our samples are:
Collected from donors with full genetic & commercial research consent
Collected & processed in a UK ISO accredited facility
Samples anonymised but traceable to origin Research Donors is:
A Human Tissue Authority (HTA) licensed establishment: License Number 12693
A Health Research Authority (HRA) ethically approved research tissue bank
Company type
Keywords
biospecimens, tissue
Dr Vashu Pamnani
LinkedIn logo Senior Business manager 

Rosemont Pharmaceuticals

Rosemont Pharmaceuticals is a UK-based pharmaceutical company that has been manufacturing and commercialising a range of prescription based liquid medicines for more than 50 years, all of which are designed for use by patients that experience swallowing difficulties / dysphagia (ie paediatric and/or geriatric patients).  

Partnering with Rosemont gives you access to our unique expertise in liquid medicines, a continuously growing portfolio of innovative medicines and the latest technology in both R&D and manufacturing. 

At our state-of-the-art manufacturing site in Leeds, United Kingdom, we produce over 4 million bottles of liquid medicine every year. Our focus on research and development is the key to growth in our portfolio and we continuously invest in our facilities to ensure we have the latest technologies to enhance our capabilities and capacity.

We have a portfolio of over 130 oral liquid medicines across a range of therapeutic areas including 70 licensed products.

All of our products, both licensed and ‘specials’ are made to the same exacting standards under GMP. Our UK range also includes 9 products licensed for use with PEG/NG tubes. We are always seeking to expand our range of medicines and covert our ‘specials’ to licensed product wherever possible.

Company type
Laszlo Kodaj
LinkedIn logo International Sales Manager Rx 

S. M. Discovery Group (SMDG)

SMDG is a biotechnology company dedicated to delivering efficacious, safe and disease modifying therapies to save lives and improve health.

Through our R&D, we are addressing the lack of safe and effective gene therapies for some of the most debilitating diseases, particularly neurological and rare diseases.  We have developed a patent protected biotechnology platform for targeted delivery of nucleic acid medicines across biological barriers, such as the blood-brain barrier and have an expanding intellectual property portfolio including granted and pending patents. 

 • Some key Highlights and Merits:  * Nature Communications (2019), 10: 4635: Crossing the blood-brain-barrier with nanoligand drug carriers self-assembled from a phage display peptide  * Nature Bioengineering Community (2019): Drug Delivery to the brain: self-assembled phage  mimetics for crossing the blood-brain-barrier

* SMDG has been recognised as a Life Science Innovator 2023 (one of UK most innovative companies) 

* SMDG’s NLC technology platform was recognized as one of the break-through and  significant/notable (findings and technologies reported) papers of 2019 by the Fluids and Barriers  of the CNS (2020 publication). * SMDG was a finalist in 2021 in the UK Bionow awards.

* SMDG’s disruptive technology has been profiled in over 160 global media outlets, journals,  biotechnology and medical news. 

* SMDG has received funding from the European Commission, UK Department of Trade, UK.  Innovation SuperNetwork, European Union Regional Development Fund, UK North East Local  Enterprise Partnership. 
Company type
Dr Z. Shadi Farhangrazi
LinkedIn logo Chief Executive Officer 
S. Moein Moghimi
LinkedIn logo Chair, Science Advisory Board and Co Founder 

Sachs Associates

Leonard Sachs
Managing Director 

Scendea

Scendea is a leading product development and regulatory consulting practice serving the pharmaceutical and biotechnology industry. We are adept at solving complex issues associated with medicinal product development and offer strategic and operational support in the fields of quality/CMC, non-clinical/toxicology, clinical/medical and regulatory. Our industry experience is demonstrable, having been involved in over 1,000 development programmes in the US and Europe over the last twenty years. As is our scientific excellence, with a team that includes ex-regulators, high-calibre academics and clinician scientists. Our technical regulatory expertise spans the entire product development spectrum from pre-clinical to marketing authorisation.
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.
Company type
Keywords
consultancy,regulatory,product development
Claire Martin
LinkedIn logo CBO 
Stuart Hunter
LinkedIn logo Senior Business Development Manager