Clinical Data Management

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...

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...

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...

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 m...

• Supervision of IBs, protocols and related documents • Initiation and follow-up of clinical trials • Selection and contact of CROs

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...

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...

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...

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...

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...

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...

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...

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...