A crucial stage in clinical research is clinical data management (CDM), which produces high-quality, trustworthy, and statistically sound data from clinical trials. This results in a significantly shorter period of time between drug development and launch.
From the time clinical trial data is recorded until it is published, we work with you to offer accurate, illuminating data management.
No matter where you are, all of your clinical data needs to be consistent.
From the time clinical data is recorded until it is reported, we deliver reliable clinical data. We can guarantee you that your data is of the finest quality available anywhere in the world because we use standard global platforms and standardised procedures.
Your data, as well as ours, never sleeps
You can take use of a 24-hour clock thanks to our infrastructure, workflow, and information technology platform. Additionally, you’ll gain from the interchangeability of our international teams because they are all qualified in and familiar with the same procedures.
Better clinical data management and analytical insights result from improved communication.
Clinical trials that are intricate and conducted globally include many moving pieces. For the purpose of coordinating both internal and external communication, we have a specialised team. This makes subject matter specialists easily accessible and ensures consistently higher-quality production.
Clinical data management, analysis, and integration from beginning to end
It can be challenging to have the internal resources necessary to manage all the data that a clinical study produces. From the moment clinical data is first acquired until it is stored, CliniMed LifeSciences can help you every step of the way. Our personnel are all trained in the same methods, which guarantees the seamless integration of your data.
Clinical Data Management
We are experts in a variety of fields and technologies with the sole intention of locking your database as quickly as possible.
The following disciplines are where you can hire us for independent, full-service, or functional outsourcing:
- Protocol design & review
- Randomization schedules
- Case report form (CRF) design & review
- Database design
- Data entry
- Data validation / verification
- Data transfer
- Medical coding
- Quality management procedures
- Data manipulation
- EDC
Statistical Consulting
In order to ensure that your study is as effective as possible, we assist you in defining the proper study components.
Biometrics
Efficiency gains from advanced programming techniques can be seen in a single study or over several studies:
- Plans for statistical analysis
- Integrated efficacy and safety summaries
- Tables, figures and listings
- Randomization code generations
- Reports from statistical and clinical studies
- Support for publications and abstracts
Clinical Data Analysis Services
- Pharmacoeconomic, QoL analysis
- Mid-study assessments with interim analyses
Integration and Warehouse Design
- Data safety monitoring boards (DSMBs)
- Establishment, governing, analysis plan creation, and maintenance