ACDM19 Sponsor Details
Sponsoring: Premier and Networking
PHASTAR is a specialist CRO offering statistical consulting and clinical trial reporting services to the pharmaceutical, biotech and medical device industries. 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.
PHASTAR is known as a CRO of quality: over the last decade, we have been involved in the design and reporting of hundreds of studies, and each has been delivered on-time and with no issues. Talk to us about using MEDRIO for your study – MEDRIO is fully functional, easy to use, and sensibly priced and PHASTAR can provide data collection as a MEDRIO partner.
uMotif is the modern data capture platform that patients love to use. uMotif’s patient-centred approach and innovative motif interface has led to the capture of over 65 million data points from more than 20,000 patients across 21 clinical conditions. Offering symptom tracking, wearable device integration, eCOA, ePRO data capture on any device. The scalable cloud-based platform is being used by top Pharma and top CROs globally.
Sponsoring: Premier Sponsor
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
Cmed is an innovative, full service technology-led CRO specializing in oncology, immuno-oncology and cell and gene therapy. Cmed brings together experienced people and technology, providing customers with a friendly, proactive service, and delivers this service using advanced clinical data capture, management and reporting software and processes. Cmed’s new generation clinical data suite, encapsia®, streamlines the capture, management and reporting of data, thus saving customers time and money.
Clinical data can be captured flexibly by eSource, multi-media and web eDC, in a single repository while being displayed in live visual insights, providing live analytics, and allowing within suite audit trailed actions. It is fully compliant with regulatory guidelines, and allows integration with existing systems. To learn more visit www.cmedresearch.com andwww.encapsia.com.
Sponsoring: Communications & Premier
Castor EDC is a user-friendly cloud solution for capturing medical research data in clinical trials. Features include self-service eCRF creation (form building), randomization, ePro (patient surveys), monitoring, easy import and export of data, EHR data importer (HL7 FHIR based), audit trails, user management, and much more. Castor EDC is currently being used by 28,000+ users across 3,600+ studies in over 50 countries.
Castor is ISO 27001 certified, GCP, 21 CFR & GDPR compliant and provides servers in the US (HIPAA compliant), the Netherlands and the United Kingdom.
Quanticate is a leading global Data-focused Clinical Research Organization (CRO) primarily focused on the management, analysis and reporting of data from clinical trials and post-marketing surveillance. As Experts in Clinical Data, Quanticate provides high quality teams that offer efficient outsourcing solutions for clinical data management, biostatistics, SAS programming, statistical monitoring medical writing and pharmacovigilance. Quanticate can offer study level support, functional service provision (FSP), strategic full data-services solutions or technical consultancy to meet the needs of pharmaceutical, biotechnology and device companies across the globe. By offering high quality, value-add client specific solutions to meet current and future development needs, Quanticate has become the supplier of choice for many companies from Top tier pharmaceutical giants through to niche biotechnology and device companies.
SGS is a leading life sciences CRO providing clinical research and bioanalytical testing, with a specific focus on early-stage development and biometrics. Delivering solutions in Europe and in the Americas, our SGS biometrics group of 300 employees offers clinical trial (Phase I to IV) services encompassing project management and monitoring, medical writing, data management, biostatistics, secure data office, PK/PD modeling & simulation, pharmacovigilance and regulatory consultancy. An early adopter of integrated IT solutions, and pioneer in full EDC application with multi-EDC systems, SGS is a CDISC-registered solution provider, with successful experience of full electronic FDA submissions for several candidate drugs.
Keyrus Biopharma is an international Consulting, Contract Research Organisation and Functional Services provider with a reputation for transparency and integrity, highly focused on being able to deliver with excellence. Our ‘human’ approach to service provision is what differentiates us from our competitors. Combined with our high caliber staff, this approach has allowed us to become a key player in clinical research.
At Keyrus Biopharma we’re proud of our commitment to delivering services of the highest quality, not only skillfully, efficiently and reliably, but also with sincerity and genuine care for our clients’ projects, priorities and reputation. Thus we maintain and advance our vision and our standards, all the while ensuring that we serve your interests better
From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical Information, Real World evidence services.
PRA Health Sciences
Arithmos is an innovative IT company with a specific focus on the Life Sciences value chain aiming to increase efficiency in different business areas: Clinical Trials conduct, Pharmacovigilance and Project Management. It is ISO 9001:2015 certified concerning Quality Management System and ISO 27001:2014 certified ensuring the compliance of Information Security Management System.
The main proprietary platforms Arithmos has developed are:
- Argus Blueprint: pre-configured, fully validated pharmacovigilance platform for the fast deployment of Argus Blueprint;
- Symphony EDC: intuitive SaaS EDC solution designed by investigators and developed by Arithmos to allow a quick and autonomous study set up and management, fully in compliance with international standards;
Arithmos also collaborates to develop solutions in the eHealth sector using big data, IoT and AI.
Enjoy your trial™ with the world’s most intuitive EDC & ePRO system
We understand the value of time and efficiency. That’s why we’ve built Viedoc using the technology of tomorrow, making electronic data capture smarter, faster and easier than ever before. We can provide you with modern tools that will revolutionise the way you conduct your clinical trials.
Less effort. More fun. Experience the power of Viedoc.
Uppsala Monitoring Centre
Inspire. Engage. Transform.
Uppsala Monitoring Centre (UMC) advances the science of pharmacovigilance and inspires patient safety initiatives all over the world. As an independent, non-profit foundation, we engage stakeholders who share our vision and collaborate to build a global patient safety culture. As a leader in the research and development of new scientific methods, we explore the benefits and risks of medicines to help minimise harm to patients, and offer products and services used by health authorities and life-science companies worldwide. Our unique expertise makes us an organisation with the capacity to transform patient safety from an ambition into a reality. For 40 years, we have provided scientific leadership and operational support to the WHO Programme for International Drug Monitoring, expanding the global pharmacovigilance network to reach more than 95% of the world’s population.
Perficient has supported hundreds of clients over more than 20 years. Our data management, medical coding and EDC services span to include amongst other:
- Medical Coding systems and support
- Advise data management teams on business optimization, digital engagement, regulatory compliance, etc.
- Full System Design, Development, Implementation and Configuration
- System Optimization and Enhancements
- Data Migration and Study Migrations
- Study Set Up and Pilots
- Custom development (reports, etc.)
- Dictionary loading / versioning
- Artificial Intelligence and machine learning
Our services are aimed to simplify and support complex business and technical challenges.
4Clinics provides clinical data management, biostatistics, SAS programming and medical writing services. 4Clinics has a global coverage and offices in Belgium, France, US, Canada and Morocco to support pharmaceutical companies, biotechnology companies and medical devices companies in their clinical development and post-marketed studies.
4Clinics provides outsourcing solutions from protocol development to study report as well as dedicated functional platforms of data managers, biostatisticians, SAS Programmers and medical writers. 4Clinics staff managed activities of more than 500 trials, performed more than 300 data analysis and wrote more than 750 clinical and regulatory documents for more than 300 clients since 2005.
We specialize in Clinical Data Management, Data Standardization and Biostatistics services. With our global experience across therapeutic areas, various EDC platforms and CDISC standards; we can definitely help you to achieve reduced timelines and improved data quality by taking a lean, proven and efficient approach. We use various EDC platforms and technologies for e-CRF, e-PRO and Quality of Life Questionnaire on mobile Application.
CRF design, CRF built and e-CRF set-up are all made by our data managers and data analysts that master all the EDC parameters to offer the maximum responsiveness and flexibility to our clients and partners.
4Clinics provides customized support for CDISC-related projects and prepare the submission package for you. The 4Clinics Data Management and SAS Programming team can guide you through the implementation of the CDISC-SDTM global standards to ensure consistency across different projects and perform the check and the conversion of legacy data to CDISC-ADaM and CDISC-SDTM standards.
Bioforum is a data focused CRO with over 10 years of clinical research experience.
We offer a wide range of clinical data services to include medical writing, data management, biostatistics and pharmacovigilance.
Our goal is to consistently improve and innovate data processes to support our clients in the utilization of their clinical data and guarantee its integrity and accuracy for the most efficient data submissions.
With a multi-disciplinary team of experts, we provide a unique and high-quality solutions for efficient collection, standardization and reporting of clinical research data. Our professional teams enable clients to manage and analyze their data through integrated visualization and analytical capabilities.
We are multinational company with offices in Israel, the US, Australia and South Africa.
OmniComm Systems, Inc. is a leading strategic software solutions provider to the life sciences industry. OmniComm is dedicated to helping the world’s pharmaceutical, biotechnology, contract research organizations, diagnostic and device firms, and academic medical centers maximize the value of their clinical research investments. Through the use of innovative and progressive technologies, these organizations drive efficiency in clinical development, better manage their risks, ensure regulatory compliance and manage their clinical operations performance. With an extensive global experience from more than 6,000 clinical trials, OmniComm provides comprehensive solutions for clinical research.
Kelly Outsourcing and Consulting, Belgium
Kelly Services has been around over 70 years as an industry leader, which initially started up as a staffing company. We are a global company with multiple service lines, meeting customers’ needs in all areas of business. With world wide strength of 8000 employees, Kelly operates in 30 countries around the globe.
KellyOCG is a global provider of workforce strategy, solutions, and operations with expertise in every aspect of the talent supply chain. Kelly provides access to some of the world’s highest-regarded scientific organizations providing you with opportunities to work on today’s most challenging, research-intensive, and relevant projects. Our organizational structure and geographic coverage has grown steadily over the years to anticipate and meet the needs of customers.
KellyOCG provides Functional Service Provider (FSP), Recruitment Process Outsourcing (RPO), Managed Service Provider (MSP) programs, Business & Professional Services, Talent Advisory Services, Career Transition & Organizational Effectiveness, and KellyConnect Managed Contact Centers, among others.
Our connections can lead you to innovative scientific pursuits you’ll be proud to help advance. We work with 99 of the Fortune 100™ companies, and found opportunities for more than 11,000 scientific professionals last year.
KellyOCG’s Functional Service Provider (FSP) program provides centrally managed solutions to Clinical Data Management, Biostatistics & Statistical Programming, Regulatory, Medical Writing and Clinical Affairs teams servicing a vast range of clients across the globe.
Medable is the first and only end-to-end (E2E) cloud platform for clinical trials, with a fully integrated, flexible suite of tools enabling patients, providers, CROs and sponsors to operate as a fully optimized clinical trial team – drastically reducing inefficiencies in bringing new therapeutics to market. Medable’s Protocol-Fit technology is configurable to the needs of each study, enabling enhanced participant enrollment, higher quality data capture, and more actionable, real-world insights. Our GCP and 21 CFR Part 11 compliant platform aggregates insights seamlessly across multiple studies, utilizing machine learning and advanced analytics to bring next generation intelligence to data collected from smart phones, connected devices, and integrated systems such as EMRs, labs, and third party APIs. We are removing silos and breaking down traditional barriers such as poor study access, ineffective screening, limited participation, and site inefficiency. Free yourself from the legacy world of ePRO, eCOA, eSource, and EDC with Medable’s E2E platform, and transform the way you work, treat, cure, and dream.