ACDM19 Exhibitor Details
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.
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.
Built by researchers, for researchers, 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 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 ISO 9001 and ISO 270001 certified IT company focused on Life Sciences industry.
Our solutions support multiple clinical trial processes enhancing efficiency and global alignment:
- Electronic Data Capture: Symphony EDC is an 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;
- Clinical Trial Management: SYNClevy is and Extended Project and Portfolio Management system developed to support clinical project managers in their daily activities’ planning and management, increasing collaboration among all company’s departments and enhancing Clinical Trial Oversight, as required by ICH GCP E6(R2);
- Pharmacovigilance: Argus Blueprint is a pre-configured, fully validated pharmacovigilance platform for the fast deployment of Argus Blueprint.
Viedoc by PCG Solutions is a global EDC and ePRO vendor with offices in Sweden (Uppsala), Japan (Tokyo) and China (Shanghai). Viedoc is a modern and future-proof EDC that allows clinical trial sponsors and study sites to easily and securely collect, validate, transmit and analyze clinical study data.
Viedoc is a proven software since 2003 which meets or surpasses all regulatory benchmarks. Designed to be as intuitive as possible, Viedoc saves time and frustration from users at every level, allowing clinical trial organizations to have more focus on their own innovation and leadership.