Member Company Listing

4Pharma is a Scandinavian contract research organization (CRO) providing medical research services to pharmaceutical, biotechnology, medical device and food companies.

Focused on biostatistics, data management and medical writing, 4Pharma employees offer you a unique blend of industry experience, service provider flexibility and the academic excellence of truly data driven mindsets.

Our core focus lies on customer satisfaction and quality of work.

With the experience of several successful global regulatory submissions, hundreds of studies we conducted for our clients (or accompanied with scientific advice) and finally our open minded dedication to science – we, the people at 4Pharma are dedicated to take you beyond your data.

Web: https://4pharma.com/

Services: Data Management, Statistics, Medical Writing

Setting a new standard in biosimilars

Alvotech is a fully integrated specialty biopharmaceutical company focused exclusively on development and manufacturing of high-quality biosimilar medicines.

Who we are

We are specialists in biopharmaceutical product creation, all along the value chain from cell line development to commercial manufacturing. Our common goal is to be a global leader in the biosimilar space and to deliver high quality cost competitive products to patients worldwide. We come from all around the world, bringing literally thousands of years of combined knowledge and expertise to our mission.

Fully in-house R&D and manufacturing provide:

Cutting-edge in-house R&D capabilities, from cell line, process and product development through process scale-up and manufacturing are completed by a fully integrated clinical and regulatory function, allowing a smooth transition from development through global launch and commercial manufacturing.

State-of-the-art facility for drug substance and drug product manufacturing of biologics, complimented by QC laboratories.

Robust manufacturing processes such as single use-technology, reducing the need to clean and sterilize equipment and allowing flexibility and multiproduct manufacturing.

What we do

Our vision as a company is to build a leading global biopharmaceutical company, while focusing on the development and commercialization of biosimilar medicines for the treatment of severe and chronic conditions, that improves the quality of life for patients around the world.

Web: http://www.alvotech.com

Amgen has more than 500 staff in the UK and Ireland, working in both the commercial and research & development organisations. The UK and Ireland commercial team operates out of our Cambridge and Dublin offices.

Amgen is one of the world’s leading biotechnology companies. Amgen is a values-based company, deeply rooted in science and innovation to transform new ideas and discoveries into medicines for patients with serious illnesses. At Amgen, we believe in a “biology first” approach. We use cutting-edge science and technology to study the subtlest biological mechanisms in search of therapies that will improve the lives of those who suffer from serious diseases. Amgen believes the cure for disease can be found inside each and every one of us.

Web: http://www.amgen.co.uk

ancillarie is a support service company established in 2012. Company provides support services in clinical research for Pharmaceutical, Biotechnology and Contract Research Organizations and helps them to accomplish their goal.

Web: www.ancillarie.com

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Contract Staffing

Anju Software makes advanced solutions for the life sciences industry from clinical operations to medical affairs that is adaptive, non-disruptive, and will enable and enhance your existing environment. The strength of Anju’s offering focuses on delivering YOUR PLATFORM, YOUR WAY. Anju will incorporate complementary solutions to YOUR environment, leveraging Anju’s integration technology, creating a tailor-made PLATFORM perfectly suited to meet YOUR needs.

Web: https://www.anjusoftware.com/

Services: Data Management, Software (EDC), Software (other)

We are not a fruit shop, but we do help our clients sort out their apples from their oranges! Established in 2018, A&O was set up as a niche Contract Service Organisation, offering custom-built reporting tools for clinical operations, data management and medical departments.

We provide off-the-shelf solutions that harness existing standard MS Office installations, requiring no additional software, that can be utilised in any clinical data environment. This approach is born out of years of knowing the ‘customer’; DMs, CTMs, Operations, CRAs, study physicians who do not want to work with heavy data listings or overly complex systems. They want a no nonsense, interactive solution in an MS Office environment that they understand. As our solutions reside outside of clinical management systems such as EDC, CTMS or external lab data, A&O can typically bridge the gap between these systems and their differing data formats (e.g. “I can see in the EDC that this patient had samples taken at visit 4, but have no idea where these samples are now”). From customised tooling to help with clinical study oversight, visit forecasting, data reconciliation (e.g. IWRS vs EDC, lab data…), medical review reports to data metrics/KPIs, A&O can assist in creating an effective solution.

If you are drowning in data and require a tailored tool to help you manage or review it, please get in touch: www.apples-and-oranges.co.uk

Web: http://www.apples-and-oranges.co.uk

Services: Data Management, Monitoring, Software (other)

At Arithmos, our mission is to support our clients in embracing digital transformation that allows them to develop therapeutics for patients in a smart, innovative, and cost-efficient manner.
Since Arithmos was founded, we helped numerous pharmaceutical, biotechnology, medical device, universities, and non-profit organisations to carry out their work in an easier and more efficient way thanks to the technology.

Web: https://arithmostech.com/

Services: Project Management, Software (EDC), Software (other), Data Collection Devices

At AstraZeneca we have transformed our pipeline and returned to growth and, as a result of continued pipeline delivery and commercial execution, we are now entering a new stage of our journey. This is focused on enhanced innovation and the delivery of life-changing medicines that that contribute value to patients and society.
The fundamentals of our strategy are clear. We focus on innovative science and leadership in our three main therapy areas: Oncology; Cardiovascular, Renal and Metabolism; and Respiratory diseases. Backed by a global presence, with strength in Emerging Markets, particularly China, we have a portfolio of specialty and primary care medicines.
At the same time, the world around us is changing and the burden of disease is increasing. We are responding by increasing our focus on growth through innovation – being more patient-centric, doing more with technology, digital and data, and advancing more cutting-edge science.

Web: https://www.astrazeneca.com/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory

Bioforum is a data-focused contract research organization (CRO), serving clients worldwide in optimizing the collection, standardization, and reporting of clinical research data. We strive to consistently improve and innovate data processes, enabling the most efficient data submissions for our clients across the life sciences industry worldwide. From our offices in Israel, the U.S., Australia, and South Africa, our multidisciplinary team provides in-depth expertise and delivers high-quality solutions, including medical writing, data management, statistical programming and biostatistics.

Web: https://bioforumgroup.com/

Services: Data Management, Statistics, Medical Writing, Software (EDC), Contract Staffing

Bionical Emas is the only CRO to combine Clinical Development, Early Access Programs and Clinical Trial Supply, to deliver a unique, seamless approach supporting our clients to bring new medicines to patients faster.

Web: https://bionicalemas.com/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory

We want survival in the UK to be among the best in the world. We’re focusing our efforts in four key areas – working to help prevent cancer, diagnose it earlier, develop new treatments and optimise current treatments by personalising them and making them even more effective.

We’ll continue to support research into all types of cancer and across all age groups. And we’re keeping our focus on understanding the biology of cancer so we can use this vital knowledge to save more lives.

We’re increasing our research in key areas such as early diagnosis, and hard-to-treat cancers including lung, pancreatic, oesophageal cancers and brain tumours.

We’re developing new tests, surgery and radiotherapy techniques, and cancer drugs. We want to personalise prevention, screening and treatment and bring benefits to patients sooner.

To help accelerate progress, we’ll be investing an additional £50 million a year into new funding schemes for our researchers. These will encourage collaboration and innovation, and support research tackling some of the biggest scientific challenges in cancer research.

Smoking is the biggest preventable cause of cancer and we’ll work towards the day when no one in the UK smokes – in particular by protecting children and helping people to quit.

We’ll campaign for the best cancer services in all parts of the UK, and give more people the chance to join the fight against cancer.

But we can’t achieve our mission alone. We rely on our dedicated scientists, doctors and nurses, and the generosity of our supporters across the UK. With your help, we can beat cancer sooner.

Web: https://www.cancerresearchuk.org/#/

Web: http://www.clinfidence.com

Services: Data Management

The Clinical Informatics Research Unit (CIRU) operates as an applied research and enterprise unit within the Faculty of Medicine at the University of Southampton. We provide clinical research solutions and services across the globe which advance data excellence, quality, management and improve research methods. Just some of the countries we work with include the United Kingdom, New Zealand, Canada, Belgium, South Africa and more.

Web: https://www.the-ciru.com/

Services: Data Management, Statistics, Project Management, Software (EDC), Software (other)

Cmed is an innovative, full-service, technology-led CRO, established in 2000 by a team of experts passionate about helping customers deliver highly successful clinical trials. We bring together an experienced team and our own innovative technology to inspire and drive real progress throughout the clinical trial process – for every step, every solution, every study. encapsia®, our new generation Clinical Data Suite is just one example of our realization of this ambition, devising new ways to drive complex clinical trials and achieve greater, speedier and more accurate results. Our vision is to conduct clinical trials better than any other CRO to help patients and ultimately save lives.

We have earned a strong reputation for successfully delivering complex, demanding and innovative clinical trials in various therapeutic areas, with considerable therapeutic expertise in both oncology and rare disease

Web: https://www.cmedresearch.com

DataClin was established in 2010 as the first Contract Research Organization (CRO) in the MENA region specialized in clinical data management, biostatistics and medical writing.

DataClin grew to be one of the top leading CROs in the MENA region working according to a full set of standards covering our scope of work, with an ongoing process of updates with regulatory requirements, and compliance to the international standards, guidelines and customer specific standards.

Web: http://www.dataclin.com

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Software (EDC), Software (other), Data Collection Devices, Freelance Data Management, Contract Staffing

DSG, Inc. is a leading global eClinical provider with a fully unified suite of innovative technology solutions and data management services for the global clinical research community. DSG’s eClinical software platform provides competitive advantage that is cost-effective with on-time project delivery. DSG solutions have been used in thousands of clinical trials around the globe with our award-winning eCaseLink™ platform and eCaseLink Designer for enterprise licensing. Founded in 1992, the company is proud to be recognized as the first provider of a fully integrated EDC and IRT Randomization and Trial Supply Management system with the SCDM Data Driven Innovation Award.

Web: http://dsg-us.com

Services: Data Management, Project Management, Software (EDC)

eClinical Solutions seamlessly orchestrates clinical technology and expertise to help accelerate the clinical development process. We provide a spectrum of customized data management services and solutions including EDC, Data Management, Clinical Reporting, and Data Standardization, as well as an innovative Clinical Data Hub platform, elluminate®, which brings advanced visualization and analytical capabilities. Through experience and innovation we empower life science organizations to manage and proactively make decisions regarding clinical trials and programs.

Formed in 2006, the eClinical Solutions team has many years of experience working in the life sciences industry dedicated to clinical data management and programming. The organization was formed to address specific needs that our Leadership team identified through their firsthand experiences, specifically to provide unique and high quality solutions for efficient collection, standardization, reporting and role based utilization of clinical research data. Through a consultative approach and the mindset realizing that each individual organization has a unique set of goals and objectives, we have been partnering with our customers to maximize the use of one of their most valuable assets, their clinical data.

Web: http://eclinicalsol.com

Services: Data Management, Software (EDC)

Eisai is one of the world’s leading research-based pharmaceutical companies. We define our corporate mission as “giving first thought to patients and their families, and to increasing the benefits health care provides,” which we call human health care (hhc). With operations in the U.S., Asia, Europe and it’s domestic home market of Japan, Eisai employs more than 11,000 people worldwide

Web: http://www.eisai.co.uk

About Excelya
Excelya is the highest quality contract research organization with the most comprehensive service coverage throughout Europe. Its 800+ employees cover 24 countries. Excelya offers all cooperation models, from consulting to functional service providing to full-service. It provides these research services across multiple industries, including pharmaceutical, biotech, medical devices, cosmetics and nutrition. As a fully integrated CRO, Excelya undertakes the design and execution of Phase I clinical trials to post-marketing studies, safety, biometrics and market access projects. Excelya is committed to providing preeminent experts who work hand-in-hand with its clients to accelerate end-to-end drug development, leverage data science and reimagine patient care.

Web: http://www.excelya.com

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Software (EDC)

Want to design and build clinical trials faster with less effort? Now you can, with our new clinical metadata repository (CMDR) and automation cloud platform, ryze. We’ve automated manual, labor-intensive processes, and given you the tools to standardize study build and integrate 3rd party platforms.
Simply house your standards and study library in the central MDR, then easily find, manage, and reuse content. Even import content from EDCs and e-clinical systems into ryze. You can design studies for leading EDCs – and see exactly how forms look in ryze without having to build your study.
Instantly convert datasets to SDTM, and make submission deliverables with the click of a button. And all effortlessly in line with CDISC standards. ryze is built on CDISC compliant templates, so compliance is enforced throughout study build. Plus, ryze is a cloud-based off-the-shelf suite, so there’s zero install and it’s ready to go when you are!

Web: https://www.formedix.com/

Services: Software (other)

Web: https://www.freeline.life/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory

Galapagos is a clinical-stage biotechnology company, specialized in the discovery and development of small molecule medicines with novel modes of action. Our ambition is to become a leading global biotechnology company, focused on the development and commercialization of novel medicines that will improve people’s lives.

Web: http://www.glpg.com

Gilead Sciences, Inc. is a research-based biopharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. We strive to transform and simplify care for people with life-threatening illnesses around the world. Gilead’s portfolio of products and pipeline of investigational drugs includes treatments for HIV/AIDS, liver diseases, cancer, inflammatory and respiratory diseases, and cardiovascular conditions.

Web: http://www.gilead.com

Our Pharmaceutical business has a broad portfolio of innovative and established medicines. We currently focus on developing new medicines in respiratory and HIV/infectious diseases, oncology and immuno-inflammation; with discovery research exploring these and other areas

Web: http://www.gsk.com

We are strategic clinical innovation experts working with biotech, academic start-ups, pharmaceutical and device companies.
Gouya Insights will translate your innovation into a clinical roadmap and design the most efficient clinical development plan.
Our experienced team provides innovative strategies to meet your goals.

Web: https://gouya-insights.com/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory

At Helsinn, we’ve made it our mission to improve the everyday lives of patients. We’ve been a family-run pharmaceutical company since we were founded over 40 years ago, guided by our values of integrity, respect and with a 360-degree approach to quality that runs through everything we do. Today, we’re leading the way in cancer care and rare diseases, and are committed to building better todays for more patients worldwide.

Web: https://helsinn.com/

We are a global healthcare intelligence partner, consistently ranked among the top CROs and best employers worldwide.

We help develop life-saving and life-improving drugs with our comprehensive clinical development services, including data management, statistical analysis, clinical trial management, medical writing, and regulatory and drug development consulting.

Web: www.prahs.com/careers

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Software (EDC), Software (other), Data Collection Devices, Freelance Data Management, Contract Staffing

The Imperial Clinical Trials Unit (ICTU) sits within Imperial College London as a department within the School of Public Health in the Faculty of Medicine and brings together academic, clinical and trial management expertise from across the Imperial College Academic Health Science Centre. ICTU also collaborates with members of the designated Academic Health Science Network for North West London – Imperial College Healthcare Partners, other national key clinical and scientific opinion leaders, other CTUs and with industry.

ICTU is a UKCRC registered Clinical Trials Unit recognised for its experience and expertise in the development and delivery of clinical trials and associated high quality clinical research projects across a range of therapeutic areas. The unit leads primarily on the design, conduct and analysis of national and international multi-centre trials and the staff, with specialist disease and methodological knowledge, have input at all stages of the trial lifecycle; thus ensuring all activities are conducted according to the principles of ICH GCP and in compliance with the appropriate regulatory and ethical requirements.

Web: https://www.imperial.ac.uk

Services: Data Management, Statistics, Monitoring, Project Management, Software (EDC)

The ICR Clinical Trials and Statistics Unit (ICR-CTSU) is a research-led, academic clinical trials unit (CTU) within the Division of Clinical Studies at the ICR.

ICR-CTSU leads the design, conduct and analysis of phase II and III national and international cancer clinical trials. Our expertise spans the whole clinical trial life cycle and our findings directly influence clinical practice within the NHS and worldwide.

ICR-CTSU clinical trials focus on breast, urological and head and neck cancers, but we also run trials in other rarer cancer types including melanoma, sarcoma and ovarian cancer. We specialise in phase II exploratory and phase III randomised trials of new treatments and technologies (including radiotherapy), and understanding cancer biology and treatment response using biomarker-driven trial designs is fundamental to our research.

We receive core funding from Cancer Research UK, are a UK Clinical Research Collaborative (UKCRC) registered CTU and one of 15 CTUs recognised by the National Cancer Research Institute (NCRI) for professional specialism in the development and delivery of cancer trials.

Web: https://www.icr.ac.uk/our-research/centres-and-collaborations/centres-at-the-icr/clinical-trials-and-statistics-unit

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management

IQVIA is a world leader in using data, technology, advanced analytics and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.

Web: https://www.iqvia.com/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Software (other), Data Collection Devices, Contract Staffing

At Julius Clinical, science is the foundation. Combined with flexibility, creativity, and innovation, our scientific approach enables fast, efficient, and high quality execution of complex clinical development programs. Our skilled and loyal networks of investigators all around the world allow us to offer superior recruitment in therapeutic area’s such as cardiology, diabetes, CNS and infectious diseases.

Our partners include leading pharmaceutical, biotech, medical device, and food companies, as well as academic investigators. We focus on clinical trials that are likely to have a major impact on medicine and on people’s lives. This type of demanding research requires more than a ‘one-size-fits-all’ approach, and our fusion of scientific and operational expertise enables to deliver results efficiently, on time and budget.

Julius Clinical has on its staff internationally recognised academic leaders who are actively involved in the design, conduct, and interpretation of clinical trials. This scientific expertise and credibility, combined with personal links with peers around the world, means that the company has a truly global reach and reputation. Through our global networks we can quickly select the most appropriate and high-performing sites to take part in a trial, and ensure that investigators are inspired and motivated.

Web: https://www.juliusclinical.com/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Software (EDC), Software (other)

The Liverpool Clinical Trials Centre is a leading UK clinical trials unit and methodological research group. We bring together a wealth of expertise built on the experience of the Liverpool Trials Collaborative which has held full registration status with the UK Clinical Research Collaboration CTU network since its establishment in 2007. We are based in the Faculty of Health and Life Sciences at the University of Liverpool, a member of the Liverpool Health Partners.

We work with the NHS and commercial partners, patients and the public to contribute to the identification and evaluation of new and innovative treatments and devices.

We have particular expertise in personalised medicine, surgical interventions, and re-purposing of and establishing evidence for existing treatments used within the NHS.

In partnership with other trials methodologists we contribute to the advancement of methods to improve the design and delivery of clinical trials.

We support the development of increased capacity for conducting clinical trials locally and nationally by encouraging the development of clinicians, healthcare professionals, and trials methodologists as leaders in clinical trial research.

What we do:

•Study Design & Grant Application
•Manage studies, including but not limited to:
◦Obtain study approvals
◦Write protocols
◦Design consent and recruitment processes
◦Develop and manage data capture and management systems
◦Develop and manage randomisation systems
◦Undertake statistical analysis
◦Data Sharing

Web: https://lctc.org.uk

Services: Data Management, Statistics, Monitoring, Project Management, Regulatory, Software (EDC), Software (other), Data Collection Devices

In an increasingly complex environment for the development and delivery of clinical trials, the Manchester Clinical Trials Unit (Manchester CTU) is here to provide the expertise you require.

Our expertise
We aim to collaborate and conduct high-quality clinical research that leads to individual and societal benefit.

Our team of over 50 staff have expertise in the design, management, analysis and delivery of multi-centre trials. These studies influence positive developments in clinical practice.

Manchester CTU (formerly MAHSC-CTU) is registered by the UK Clinical Research Collaboration (UKCRC) and receives funding from NIHR, CRUK, The University of Manchester and Health Innovation Manchester.

What is a CTU?
Clinical trials units (CTU) are specialised biomedical research units which design, centrally coordinate and analyse clinical trials and other studies.

Web: https://www.bmh.manchester.ac.uk/manchester-ctu/

Services: Data Management, Statistics, Monitoring, Project Management, Software (EDC), Software (other)

Medical Agency for Research and Statistics is a clinical research consultancy and training corporate. #MARS provides several services for clients in the Clinical, bioequivelance, biotechnology and medical device sectors، both academic and regulatory:

Medical writing
Clinical data management
Biostatistics
Training courses

Web: http://www.marsresearchhub.com

Services: Data Management, Statistics, Medical Writing, Project Management, Freelance Data Management

The Medicines Evaluation Unit (MEU) Ltd is one of the UK’s leading contract research organisations, and a facility where commitment to excellence is paramount. Possessing extensive pharmaceutical, scientific and clinical expertise, allied with fast volunteer recruitment, both healthy and patient, within a state-of-the-art hospital based research facility, enables the MEU to offer clients positive clinical trial solutions.

The MEU’s bespoke database and trial management system I.C.A.R.U.S. assists recruitment of the right patient to the right study, facilitating rapid enrolment, allowing us to meet our clients’ timelines.

The MEU holds MHRA Phase I Accreditation, together with an MHRA Manufacturing Assembly Licence, enabling the company to perform assembly activities. We can also offer a full CRO service with our well-established partners.

Web: http://www.meu.org.uk

Our Data Centre Hub is based at the Micron UK office, and from here we can meet all of your data delivery and statistics needs, from initial study design through to statistical analysis and reporting

Web: http://www.micron-group.com

NICTU is a UK Clinical Research Collaboration (UKCRC) fully registered clinical trials unit. It has a specific remit to provide support for the design, conduct, analysis and publication of clinical trials and other well designed studies.

The aim of the NICTU is to support partnerships between academic clinicians and health service researchers by providing the infrastructure to facilitate the delivery of high quality clinical research funded by the National Institute of Health Research (NIHR), UK Research Councils and charities.

The NICTU are keen to collaborate with colleagues on clinical trials and other well designed studies, to provide a range of services including planning the outline proposal, through the successful running of the project to the dissemination of the results.The NICTU will generally collaborate on projects in any area of health or social care and these studies are typically funded from external sources.

The NICTU team has a broad range of research expertise across clinical research in clinical, community and general practice settings.

Web: http://www.nictu.hscni.net

The Norwich Clinical Trials Unit (NCTU) works with sites and institutes across the UK to deliver high quality studies.

We received full registration status from the UKCRC in 2013, and have been successfully re-registered in 2017 (UKCRC press release).

We are based within the awarding–winning Norwich Medical School at the University of East Anglia, and we work closely with the Research Design Service East of England and the Norfolk and Norwich University Hospital.

We have a large and established portfolio of studies within core areas of strength which reflect the interests of our world-class researchers

Web: http://www.uea.ac.uk/norwichctu

At Nutricia Research we believe that every consumer and patient deserves optimal nutritional support. We use life science, food science and technology, together with the passion, drive and expertise of over 900 employees, to pioneer nutritional solutions for those with special nutritional needs

Web: https://www.nutriciaresearch.com

W h a t m a k e s u s d i f f e r e n t ?

Apart from all the standard features you would find in a typical off-the-shelf EDC & eSource platform (which we have), we also offer the following:

– Integrated IRT within the EDC
– ePRO using device agnostic technologies
– Integrated Medical Coding (MedDRA) + WHO-DD in Development
– Standalone or Integrated Pharmacovigilance Platform
– Centralized Library of re-usable forms & edit checks

+ Fully Integrated eSource & eCRF option, reducing the need for transcription and reducing the needed for SDV

Web: https://nuvoteQ.io

Services: Software (EDC), Software (other), Data Collection Devices, Freelance Data Management

We provide the pharmaceutical industry with an alternative approach to clinical trial design and management. We help you safely accelerate drug development programs, thereby enabling critical new drugs to reach patients faster. We are the leading experts in the field of electronic health records (EHRs) enabled randomised clinical trials (RCTs). We provided the technology that enabled the success of the Salford Lung study and are the only organisation in the world to have evaluated the safety and effectiveness of a pre-license medicine in a real-world setting

Web: https://nweh.co.uk

Services: Software (other)

The Peninsula Clinical Trials Unit (PenCTU) is a leading academic clinical trials unit, with expertise in designing, developing, supporting and co-ordinating high quality, multi-centre clinical trials and other well-designed studies that will directly influence clinical and healthcare practice.

PenCTU is a fully registered clinical trials unit in the UK Clinical Research Collaboration (UKCRC) and currently receives National Institute for Health Research (NIHR) CTU support funding. This funding has been awarded to support the Unit in developing and supporting NIHR research.

The PenCTU works in partnership with clinicians, researchers, the NIHR Research Design Service South West, the Clinical Research Network and other partners from across the South West Peninsula and beyond, starting with the funding application, to deliver the full spectrum of clinical trial expertise to applicable standards and regulations.

Web: https://www.plymouth.ac.uk/penctu

Services: Data Management, Statistics, Monitoring, Project Management, Regulatory, Software (EDC), Software (other), Data Collection Devices

PharMarketing GDPR Life Sciences is an operational consulting company based in France and acting in Europe. We help companies to become compliant with Data Privacy European Law EU GDPR (eugdpr.org), with US Privacy Shield, GCP and IT Good Practices (ISO 27001). We also provide Legal Representation in the EU for Clinical Research, for GDPR and deliver Audits Services of IT systems, of business processes, of quality compliance, etc. We are dedicated to organisations in Life Sciences sector manipulating Patients’ Data.

Web: https://www.pharmarketing.net/

Services: Data Management, Regulatory

PHASTAR is a specialist CRO offering statistical consulting and clinical trial reporting services to the pharmaceutical industry. Our number one priority is to ensure the work we produce is of the highest quality: every project PHASTAR undertakes is supervised on methodology and utilises unique internal processes designed to ensure the best quality.

Our aim is to provide a service that is ahead of our competitors: in the last 2 years, we have been involved in the design and reporting of over 200 studies, and each has delivered on-time and with no quality issues.

We can provide data collection as a MEDRIO partner. Talk to us about using MEDRIO for your study – MEDRIO is fully functional, easy to use, and sensibly priced.

Web: http://www.phastar.com

PPD is a Leading Global Contract Research Organization Focused on Delivering Life-Changing Therapies

As a global provider of clinical development and laboratory services, focused on operational excellence, we improve health by helping customers deliver life-changing medicines. Patients are always at the heart of our work. This is what drives us to continually reimagine – and reformulate – the future of pharmaceutical product development. We deploy our passion, innovative spirit and an exceptional span and quality of solutions to demonstrate the effectiveness, safety and value of new therapies.

Web: https://www.ppd.com/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory

Our Approach
Continually optimizing our processes to deliver the right mix of agility and knowledge to support our most innovative biotech and specialty pharma sponsors.

What we do
Your compound shows spectacular promise, but it seems there’s an obstacle at every turn – finding hard-to-reach patients, defining relevant endpoints, navigating the regulatory maze, and ultimately obtaining clean, conclusive data.
Our Built for Biotech model is a compilation of the most successful techniques and capabilities observed across our experience, applied to provide a specialized customer experience.

Our approach in action
Therapeutically focused teams of clinical professionals have the knowledge and experience necessary to effectively manage any situation that may arise in your trial. Our approach is firmly grounded in comprehensive project management principles and well-defined processes.

Web: https://premier-research.com/

Services: Data Management, Statistics, Medical Writing, Monitoring, Project Management, Regulatory, Data Collection Devices, Contract Staffing

Our mission is to be the greatest CRO in the world as measured by our employees, clients, and sites. We meet deadlines and enrollment milestones, time and time and time again. We listen and anticipate our sponsors’ needs before they even know them. We dedicate ourselves to success on every level of our company.

Simply put, working with us gets you more: More passion. More results. More success.

Web: https://www.psi-cro.com

Globally, Roche is the world’s largest biotech company, with truly differentiated medicines in oncology, immunology, infectious diseases and neuroscience. Roche is also the world leader in in vitro diagnostics and tissue-based cancer diagnostics, and a frontrunner in diabetes management. Roche’s personalised healthcare strategy aims at providing medicines and diagnostics that enable tangible improvements in the health, quality of life, safety and survival of patients. Twenty-eight medicines developed by Roche are included in the WHO Model Lists of Essential Medicines, among them life-saving antibiotics, antimalarials and chemotherapy. Roche in the UK employs over 2,000 people in pharmaceuticals and diagnostics

Web: https://www.roche.co.uk

In July 2015, bioCSL and the influenza vaccines of Novartis joined forces to create Seqirus, now the second largest influenza vaccine company in the world. Cutting-edge facilities, technologies and technical expertise, Seqirus will be a reliable supplier of seasonal influenza vaccine with the ability to rapidly respond to pandemic threats

Web: http://www.seqirus.com

TFS was founded in 1996 and has grown to become the leading global mid-size clinical CRO focusing on small and mid-size life science customers. TFS employs more than 700 professionals throughout 21 countries and currently delivers clinical research services in more than 40 countries. We can provide end-to-end solutions or flexible single services. Our partnering approach with customers is based on our four business principles – commitment, flexibility, value creation and global reach. Our core therapeutic specialties are Dermatology, Oncology, Ophthalmology, Immunology, CNS, Cardiovascular and Endocrinology.

Web: https://www.tfscro.com

Web: https://www.gla.ac.uk/researchinstitutes/healthwellbeing/research/robertsoncentreforbiostatistics/

Services: Data Management, Statistics, Monitoring, Project Management

For over 20 years, Vitaflo® has been at the forefront of developing innovative specialized clinical nutrition products for Inborn Errors of Metabolism (IEM), nutrition support and disease specific conditions such as renal disease.
Working in partnership with world key opinion leaders and patients, Vitaflo’s research and development team conducts clinical trials on all our products with leading centers around the world.
Vitaflo’s aim is to create products that combine the best of cutting edge research with the lifestyle demands of modern living, ensuring the most acceptable products are available for the patient.

Web: https://www.nestlehealthscience.co.uk/vitaflo

Worldwide Clinical Trials employs more than 1,400 professionals around the world, with offices in North and South America, Eastern and Western Europe, Russia and Asia. One of the world’s leading, full-service contract research organizations (CROs), we partner with sponsors in the pharmaceutical and biotechnology industries to deliver fully integrated clinical development and bioanalytical services, extending from first-in-human through phase IV studies

Web: https://www.worldwide.com

WriteSource Medical Pty Ltd is an Australian based medical writing and biostatistics consultancy with a global client base. We combine the power of statistics with the ability to communicate them.
At WriteSource Medical, we pride ourselves on providing accurate, ethical and balanced services to the pharmaceutical and academic sectors. We also offer training in biostatistics and medical writing. WriteSource Medical Pty Ltd works closely with you to understand and meet your needs. We comply with relevant industry standards for data management, medical writing and biostatistics.

Our highly qualified team includes biostatisticians, data scientists and medical writers.

Web: http://writesourcemedical.com.au

Services: Data Management, Statistics, Medical Writing, Project Management

The York Trials Unit provides a number of services including study design, randomisation, trial coordination, data management, statistics, economic evaluation and outcomes. We also run a number of courses about clinical trials. More information on both historical and currently active trials can be found in the relevant project microsites

Web: https://www.york.ac.uk