Member Company Profile

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.

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.

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.

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.

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

Aptus Clinical is a specialist UK-based Clinical Contract Research Organisation (CRO) with particular expertise in oncology, rare diseases and advanced, cell and gene therapies. We have decades of experience in delivering complex and innovative trials, transforming potential into value.

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

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.

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.

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.

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

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.

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, data quality, data 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.

Our Lead products are EDGE, our Research Management Programme and CORE for Clinical On-demand Research.

EDGE is a global clinical research management system which is embedded into the clinical research infrastructure across 80% of England’s NHS regions, as well as prominently across Scotland and Northern Ireland. Overseas, EDGE is utilised in Canada, New Zealand, Belgium, South Africa, and India. The EDGE Programme offers a unique approach to the management and conduct of research through purpose-built software and provides research professionals with fast access to real-time data. EDGE enables users to track and manage studies from start to finish as well as providing complete control and oversight of patient and participant recruitment. EDGE promotes collaboration throughout its software and improves methods of working, ultimately resulting in better patient care and treatments.

CORE covers a range of expert services which include the design, build and running of electronic forms used in clinical trials across the UK and overseas, including countries such as New Zealand, Brazil, Switzerland and Turkey. Not only does CORE create the forms you need, it also offers randomisation, data management and provides you with those all-important study statistics. CORE captures vital data for researchers working both in the academic world and commercial setting.

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

Clinion is a global clinical technology company that offers AI-enabled eClinical solutions. ClinionAI consists of EDC, RTSM, CTMS, eCOA and Document Automation that cover the entire clinical trial lifecycle. Clinion is committed to innovating the future of clinical trials through ClinionAI and empowering its partners to manage trials more efficiently at lesser costs.

Services: Software (EDC), Software (other)

ClinoSol Provides Trainings and Resource consulting in the field of Clinical Research and Clinical Data Management.
Training and development play a pivotal role in the performance of organizations as well as the self-fulfilment of their employees. In the recent years, skilled and job-ready workforce for the corporate organizations, especially in a patient-centric world has become the need of the hour. ClinoSol, established in 2019, with its personalized gap-filling training structure sculptures the academic knowledge to the real-world skills in various most popular Clinical Research domains and connects these talents through our channelized resource consulting services across the nation and overseas.

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

Datacapt provides an easy-to-use, flexible, and powerful electronic data capture platform (EDC) for on-site, hybrid, or decentralized Clinical Trials. We allow Sponsors, CROs, Sites, and Patients to work together. Our Platform brings simplicity, efficiency, and quality to the collection of clinical data.

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

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.

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

Debiopharm is an independent biopharmaceutical company based in Switzerland with an ongoing commitment to improve patient outcomes and quality of life in oncology and bacterial infections. Our main activities include drug development, drug manufacturing and digital health investment.

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.

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

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!

Services: Software (other)

We are a fully integrated biotechnology company focused on discovering, developing, and commercializing innovative medicines. We are committed to improving patients’ lives worldwide by targeting diseases with high unmet needs. Our R&D capabilities cover multiple drug modalities, including small molecules and cell therapies. Our portfolio comprises discovery through to Phase 4 programs in immunology, oncology, and other indications. Our first medicine for rheumatoid arthritis and ulcerative colitis is available in Europe and Japan.

George Clinical is a leading global clinical research organization founded in Asia-Pacific headquartered in Sydney, Australia, driven by scientific expertise and operational excellence. With over 20 years of experience and more than 400 people managing 39 geographical locations throughout the Asia-Pacific region, USA, and Europe, George Clinical provides the full range of clinical trial services to biopharmaceutical, medical device, and diagnostic customers, for all trial phases, registration and post-marketing trials. George Clinical combines scientific and clinical leadership with expert trial delivery to create distinctive world-class solutions.

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

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.

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

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.

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.

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.

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.

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

Insights Research Organization & Solutions (IROS) is the first UAE-based Contract Research Organization (CRO) specializing in healthcare research. From clinical trials across all therapeutic areas to integration of real-world data, we provide the highest international ethical and scientific standards in clinical trial management, as well as key insights that lead to innovative, life-changing treatments.

While the drug discovery process is complex and critical, the clinical testing and validation phase is equally crucial, requiring procurement of proper resources and efficiency for optimal outcomes. IROS, with its expertise in data research, project management, testing, and trials, enables pharmaceutical companies to develop new medicines and drugs in a cost-effective manner, which will allow them to enter new products to market more efficiently. Our facilities meet the highest standards and optimize results through professional, productive teams and groundbreaking technologies that support and add value to research from conception to commercialization at national and international levels.

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

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

KCR is a clinical development solutions provider creating value for biotechnology and pharmaceutical organizations.

Founded in 1997, our expert teams support clients with full-service clinical development capabilities across four main areas: Trial Execution, Consulting, and Placement .

KCR operates across North America, Europe, and Australia, with main office locations in Boston, US; Berlin, Germany; and Warsaw, Poland. Our geographical coverage across 25+ countries, cutting-edge technical capabilities and tailored offerings allow for the optimized delivery of solutions to develop life-changing therapies.

KCR offers access to an estimated population of 1.1 billion people.

For more information visit www.kcrcro.com

We see the human behind every number.

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

Lokavant is a clinical intelligence platform that improves the time, cost, and quality of trial planning and execution through data-driven analytics applications. Lokavant’s platform aggregates and integrates real-time data from disparate trial data sources, and powers advanced analytics enabled by its compendium of proprietary trial data. The suite of applications built on the platform allows study teams to proactively plan and manage their studies and surface insights, driving efficiencies in all scientific and operational use cases. To learn more visit www.lokavant.com.

Services: Data Management, Monitoring, Software (other)

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.

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

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

Mednet is a healthcare technology company specializing in eClinical solutions designed for the global life sciences community. Mednet’s comprehensive, EDC-centric eClinical platform improves the efficiency of clinical studies of all types and sizes. Beyond electronic data capture (EDC), Mednet’s solution set provides the tools required to build and manage all types of clinical research, while enabling organizations to adapt to evolving demands and requirements. Pharmaceutical, medical device, biotechnology and Contract Research Organizations (CROs) around the world have trusted Mednet for nearly 20 years to deliver the technology innovation, experience and reliability they need for success.

Our platform, iMednet, is a comprehensive, cloud-based, clinical data management system, centered around a robust EDC and built from the ground up with key native modules, including: Randomization, Trial Supply Management, Adjudication, ePRO, Payments, and DICOM Imaging.

Designed to also allow easy integrations, the platform enables research teams to meet the rapidly evolving requirements of clinical research, while supporting a wide range of study types and designs. iMednet is highly flexible and intuitive, enabling users to get studies up and running quickly, while ensuring easy onboarding of the entire research team and clinical trials sites.

Services: Software (EDC), Software (other)

At Medrio, we believe that clinical trial technology shouldn’t be difficult to use. That’s why our full-service eClinical Data Management suite helps streamline your research and unify your solutions so you have more time to focus on your patients, rather than multiple vendors. Since 2005, our flexible technology has evolved alongside our customers to include an integrated suite of EDC, DDC, eConsent, RTSM and ePRO/eCOA solutions that support your teams and sites, while reducing patient burden.

Let our solutions put you back in the driver’s seat with adaptive technology that easily powers mid-study changes and accelerates your trials, without compromising data quality. Or lean on our global team of experts who are available 24/7 to support you where you need it most. We’ve worked alongside Sponsors, CROs, and sites—spanning all therapeutic areas and trial phases—to secure over 770 approvals, because we know it takes a village to achieve a healthier world. Discover the Medrio difference today by visiting us at medrio.com.

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

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.

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

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

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.

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

Pharma14 is a leading global medicine database platform used by a wide spectrum of life science companies. Our monthly updated platform is used by governmental agencies, pharmaceutical companies, consultants, CMO’s, API manufacturers, wholesalers and pharmacy retail chains. Pharma14’s robust and accurate medicine data, as well as its industry leading drug pricing reimbursement information give its members the tools required to compete in today’s market. Key pricing drivers such as generics, parallel trade, biosimillars, niche markets and more provide unique industry insight.

Pharma14 can help you.
Track and analyze pricing and reimbursement environments.
Find and create your optimal product launch pricing.
Track historical price movement.
Live track first generics entering the market and create future strategy for loss of exclusivity.
Navigate dossier submission landscape.
Enter price negotiations with full information.
Create and track your own IRP (International Reference Price) data.
Seek out niche markets and products.
Track consumption and sale trends.

Pharma14 full highlights:
• 68 full country medicine database. https://www.pharma14.com/StaticPages/Features
• 2,500,000 medicines (Rx and OTC) – full information about each drug including – Ex-factory, Wholesale and retail prices + reimbursed information.
• Active ingredients, ATC code classification, administration routes, strength, trade names, MA holder information, leaflets in PDF format and much more.
• Niche market product locator.
• Market Opportunity Locator business tool. Live track the molecules with the least competition per country.
• Consumption and sales data for USA, EU5, Scandinavia, Baltics, Canada and more.
• Full European parallel import information. EMA and National levels.
• National medicine shortages tracker.
• First approval date and marketing authorizations for all molecules from USA, Europe.
• Standard monthly updates.
• Real manufacturer information.
• Most competitive and affordable

Services: Software (other)

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.

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.

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.

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.

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.

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

Science4Tech’s mission is to facilitate access to multiple innovations enabled by technology to improve the quality, rigour and a reliable clinical research based on the scientific method, supporting pharmaceutical and biotech companies in the acceleration of drug development to bring much-needed therapies to patients sooner.

Our data-driven solutions aim to improve all stages of clinical trials, under strict scientific rigour and in compliance with the regulatory framework.

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

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

Services: Data Management, Statistics, Monitoring, Project Management

Proven global expertise in rare/ultra-rare disease therapeutic development, with bold scientific strategies and a team unafraid of the big thinking required to get your novel therapy to patients everywhere – quickly, safely, and cost-effectively. ​

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

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.

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.

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