Medidata is reinventing global drug development by creating the industry’s leading cloud-based solutions for clinical research. Through their advanced applications and intelligent data analytics, Medidata helps advance the scientific goals of life sciences customers worldwide. This includes nearly 800 global pharmaceutical companies, innovative biotech, diagnostic and device firms, leading academic medical centers, and contract research organizations.
The Medidata Clinical Cloud® brings a new level of quality and efficiency to clinical trials that empowers their customers to make informed decisions earlier and faster. Their visionary and unique clinical trial data assets provide deep insights that pave the way for future growth. The Medidata Clinical Cloud is the primary technology solution powering clinical trials for 17 of the world’s top 25 global pharmaceutical companies, from study design and planning through execution, management and reporting.
Veeva Systems Inc. is a leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, Veeva has more than 800 customers, ranging from the world’s largest pharmaceutical companies to emerging biotechs.
Veeva Vault Clinical Suite is a comprehensive suite of clinical applications, offering EDC, coding, data management, study start-up, eTMF, CTMS, and payments in a common cloud platform. Life sciences companies can increase visibility, streamline end-to-end processes, and improve how sponsors, CROs, and sites work together throughout the clinical trial process.
Viedoc by PCG Solutions is a global EDC system empowering organizations with a modern and future proof solution for Clinical Trials Data collection.
Viedoc allows clinical trial sponsors and study sites to easily and securely collect, validate, transmit and analyze clinical study data.
Viedoc meets all applicable regulatory standards, including ICH GCP, 21 CFR part 11, HIPAA.
It has been used in over 1200 trials in more than 70 countries in all therapeutic areas and clinical phases since 2003.
Mednet is a healthcare technology company specializing in eClinical solutions designed for the global life sciences community. Mednet’s all-in-one eClinical platform improves the efficiency of clinical studies of all types and sizes. Beyond electronic data capture (EDC), Mednet’s comprehensive 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.
Medrio is the first true Software as a Service technology created specifically for clinical study data management. Medrio merges the concept of cloud-based computing with a robust, secure, and regulatory compliant EDC software. The result is an EDC platform that empowers any study – faster, lower cost, and more control.
Medrio has been used to collect data in a vast array of therapeutic areas, all study phases, and in more than 40 countries around the world. The software is in compliance with regulations such as 21 CFR Part 11, Annex 11, European Privacy Shield/GDPR, Good Clinical Practice and HIPAA.
UMotif is the leading modern data capture platform for research, that patients love to use. With industry leading expertise in Real World and non-interventional studies, the engaging and clinically-proven platform captures e-consent, eCOA / ePRO, symptom and wearable device data. Working with top pharma, CROs and e-clinical platforms, uMotif can be deployed quickly across the world in any condition.
4G Clinical is a leader in randomization and trial supply management (RTSM) for the global life sciences industry, offering the only fully cloud-based, 100% configurable and flexible solution utilizing natural language processing (NLP) and integrated supply forecasting.
Our unique approach to RTSM allows us to respond and react quicker than ever before so we can bring crucial medicines to those who need them, faster.
Founded in 2000, MWB Consulting is now a premier boutique pharmaceutical consulting firm focused on the development and support activities in the pharmaceutical and medical device industries. MWB’s clients range from large pharmaceutical companies to small biotech companies in Europe, North America and Latin America.
MWB currently provides QPPV and pharmacovigilance consulting services and assist clients in resolving difficult product safety issues at the regulatory level.
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