Clinical Data Management Efficient clinical data management is the key to successful trials. Discover the impact of instant collaboration and real-time data.
Clinical Data Management Efficient clinical data management is the key to successful trials. Discover the impact of instant collaboration and real-time data.
Save Time & Enhance Quality
Our clinical data management services are designed to ensure the highest standard of data accuracy, compliance, and management throughout your trial’s lifecycle. We consistently surpass industry expectations by applying our innovative thinking, cutting-edge technology, and deep industry expertise. Our data collection, processing, storage, and analysis techniques are far beyond those of our competitors.
ACDM Awards Finalist
ACDM Awards 2024 finalist for “Team Excellence in the Management of Clinical Data“
Our clinical data management process ideally begins at the protocol design phase of a clinical trial, where our expert clinical data managers (CDMs) analyze and provide input into the protocol. This guarantees a thorough alignment between the protocol and data capture instrument design. Employing a meticulous approach, we ensure that the participant journey is accurately represented in the final eCRF and data capture instruments, facilitating seamless navigation for site staff and maintaining logical trial flow. This attention to detail is paramount to ensuring that clinical trial data is reliable, accurate, complete, and verifiable.
A well-structured CRF is essential for accurate and efficient data collection. Our designs mirror the participant’s journey, reducing errors, minimizing queries, and optimizing data entry workflows to improve study conduct.
We help you run smoother, faster, and more reliable clinical trials. Our team supports you with everything from setup to clean, accurate data. We are here to make your work easier and your results stronger.
Our team ensures precise and error-free data collection and processing.
Streamlined data handling, from collection to analysis, saving time and resources.
Our CDM experts implement robust security measures to protect sensitive trial data.
We provide immediate access to data and insightful reporting for timely decision-making.
Looking for Clinical Trial Support That Fits Your Study?
Explore how our flexible, integrated services can help you accelerate timelines, improve quality, and reduce complexity.
We want every conversation to be focused and helpful. These FAQs are a good place to start.
Our service includes comprehensive management of clinical trial data, from collection and validation to analysis, data monitoring and reporting. We ensure quality, accuracy, timeliness, and compliance with regulatory standards.
We implement robust security protocols, including encryption and access controls, to safeguard sensitive trial data against unauthorized access and breaches.
Absolutely, we understand that not all trials can be accommodated in the same manner. We offer customizable data solutions tailored to meet the unique requirements of each clinical trial. We consult with you to come up with a tailored suite of services that match your needs.
Our services provide advanced clinical data analytics tools and real-time reporting features, enabling insightful data interpretation, reducing risk, increasing quality and decision-making. All tools ensure quality, accuracy, and compliance with regulatory standards and guidelines.
Our team are experts in their respective fields and are well versed regarding global data standards and regulatory guidelines, ensuring comprehensive compliance throughout your trial's clinical data data management process. Our extensive quality control systems have been developed exactly for our services and SOPs. This means all our deliverables are of the highest quality and exceed all regulatory requirements.
Let’s Make Things Simple
Learn more about how we can support your clinical trials.
SPEAK TO AN EXPERT
Beyond protocol development, Wemedoo offers a comprehensive suite of integrated data operations services for clinical trials. At each step, we ensure your trial meets the highest quality and regulatory standards, while streamlining your clinical trial processes and saving you time and money. Discover our other services, all focusing on innovation and excellence in clinical research.
oomnia - Meeting Industry Standards
Our unified clinical trial software is designed with compliance at its core, meeting critical industry standards. Our commitment to these regulations ensures that your clinical trials are not only efficient but also adhere to the highest levels of data integrity, privacy, and ethical conduct.
21 CFR
PART11
compliant
HIPAA
compliant
GDPR
compliant
ICH GCP
compliant
SWISS DATA PRIVACY LAW
compliant
FAIR ALCOA+
compliant
Read more about the experiences from those who have partnered with us
All jobs, both large and small, are performed with the same dedication to quality, detail, innovative thinking, and rigor. It is always a pleasure to work with the Wemedoo team.
Georg Mathis, PhD
CEO Appletree CI Group AG
Wemedoo embodies all the traits desired in a partner in the clinical trial industry – expertise, innovation, reliability, compliance, and attention to detail.
Martina Diminic Smetisko, DMD
Managing Director at Marti Farm Ltd
Their dedication to, and support of, our projects has resulted in clear quality deliverables. They are always there to answer any questions with expertise in a timely manner. I am looking forward to our next project together.
Volodymyr Stus, MD
Biopharmaceutics and Clinical Research Department Manager at Polpharma SA
Everything You Need Working as One?
Experience oomnia, our all-in-one clinical trial software which unifies tools, such as EDC, eSource, RTSM, eTMF, ePRO, eCOA, eConsent, and CTMS. Combined with our professional services, we support you end-to-end to run faster, cleaner, and more efficient trials.
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