Clinical Data Management
Clinical Data Management Companies (18)
Clinical Data Management News
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News Tracking Innovation with LODAAT Pharma: CPHI Frankfurt Track Interview
CPHI Frankfurt, to be held at Messe Frankfurt from October 28–30, 2025, will once again bring the pharmaceutical industry together for 3 days of collaboration and innovation. Our interview series sits down with some of our conference track ... -
News AstraZeneca to invest US$2.5 billion in Beijing R&D centre
Amid investigations of former AstraZeneca China head Leon Wang in 2024, AstraZeneca have outlined plans to establish its sixth global strategic R&D centre in China. Their aim is to further advance life sciences in China with major research and manufact... -
News The Data Revolution: How Real-World Evidence is Changing Pharma
A look at the companies extracting valuable insights from health data to accelerate clinical development and support regulatory decision making.
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News Adaptive clinical trial success calls for flexible approach
Adaptive clinical trials have accelerated COVID-19 vaccine development and could make drug R&D more efficient but running such studies is complex and challenging and sponsors need to prepare, say experts
Clinical Data Management Products (16)
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Product Early Phase Clinical Study Expertise
State-of-the-art phase I/ll unit supporting complex clinical trials First in Human ( FIH) to Proof of Concept ( PoC) Clinical pharmacology studies through all phases In-house safety lab and bioanalytical services Special patient populations (with a focus on respiratory) Data management, regulatory sup...
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Product Formulation Development
Quotient Sciences has almost 30 years of experience developing a breadth of pharmaceutical formulations across a range of indications. Our innovative approach to formulation development integrates drug product development with clinical evaluation, combined with our experience with over 1,000 molecules at a...
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Product Biostatistics and Data Management
With 25 years of experience, Lambda Therapeutic Research is a trusted full-service CRO delivering excellence in Biostatistics and Data Management—two essential pillars of successful drug development. Our team of data managers, biostatisticians, statistical programmers, and pharmacokinetic specialists ensur...
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Product Data Solutions
The importance of Data Analytics and the need for Power BI to visualize and manipulate your data has never been higher. Our extensive knowledge in Data Engineering and Data Migration can help you integrate and load data from multiple sources to a unified data repository. We specialize in ETL Processing and...
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Product Data Sciences
You need data rapidly to make crucial decisions during a study. Faster data means we can provide our customers with earlier interim data and interim PK reports for on-study dosing and formulation decisions.
We understand on-study changes to early phase study designs and d...
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Product Printed Pharmaceutical Literature
CCL Healthcare’s printed literature options are designed to meet the regulatory, multilingual, and instructional demands of the healthcare packaging industry. Our wide range of high-capacity folded package inserts, outserts, padded inserts, booklets, glued pads, and more provide ample space for detailed le...
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Product Res_Q
Res_Q helps IT and quality leaders eliminate validation debt, achieve peace of mind and untangle valuable resources. Res_Q's data-focused architecture and wide array of industry-supported applications prevent you from falling deeper into validation debt with every new software release.
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Product Clinical Data Management
Clinical Data Management (CDM) is a critical component of clinical research and clinical trials, ensuring the accurate collection, validation, analysis, and reporting of clinical trial data. Key Concepts and Processes in Clinical Data Management:
1. Data Collection.
2. Data Validation and C...
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Product Data Management
Clinical Data Management Services include: For Study Startup activities we're doing - Protocol Review, CRF Creation, Development of Data Management Plan, Database Build: eCRF Specification, eCRF Programming, Data Validation Plan, Edit/SAS Check Programming, Dataset Extraction and Review, eCRF Completion Gu...
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Product Clinical Research Solutions
We design and execute clinical trials so new therapies get to market in the quickest and safest way possible. Full-Service Solution: We manage and execute full-service clinical trials across major therapeutic areas within medical device, diagnostics, drug, and biologic. Functional Service Provisi...
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Product eClinical suite
The Clinvigilant eClinical suite includes: EDC, eCRF, eTMF, eSource, IWRS, ePRO, eConsent and eCOA. Just pick the tools that you need and we will integrate them with your existing software ecosystem.
Clinvigilant is a global cost-effective eClinical tools provider for Pharma, Biot...
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Product Clinical Trial Services
Our experts will accomplish your clinical objectives by leading the way from recruitment strategies, site selection, and clinical logistics, all the way through the regulatory process.
We use our own eClinical suite to be more cost-efficient and keep you connected remotely acros...
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Product Clinical Trials and Bioequivalence Studies, Clinical Services, Bioanalysis
ACDIMA BioCenter is a comprehensive clinical CRO based in Jordan and founded in 2000. ACDIMA BioCenter is a multinational investment operates as business-driven model with focus on supporting the industry of clinical trials and bioequivalence studies services that help expediting their regulatory a...
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Product Clinical Data Mangement and Statistics
At ProRelix Research we are a team of experienced people who are well aware of 21 CFR, HIPAA, ICH GCP compliance to provide clinical data management services. Our statisticians have extensive experience in various phases of clinical trials and different therapeutic areas. Working on a project, our team see...
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Product Medical Writing
At ProRelix Reseach wiith the unique blend of medical writers comprising of doctors, pharmacists, scientists and grammar experts, ProRelix provides medical writing services from essential documents such as study synopsis and protocol, clinical study report (CSR), investigator’s brochure (IB) informed conse...
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Product Clinical Department
• Supervision of IBs, protocols and related documents • Initiation and follow-up of clinical trials • Selection and contact of CROs
Upcoming Events
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CPHI & PMEC China 2026
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25 Aug 2026 - 27 Aug 2026


