4Clinics
4clinics is a company dedicated to providing comprehensive clinical research services, including data management, biostatistics, medical writing, study management, clinical operations, regulatory affairs, and scientific communication. They aim to support pharmaceutical and biotech companies in their clinical development processes, ensuring high-quality and compliant research outcomes.
Industries
Nr. of Employees
medium (51-250)
Products
Biostatistics
Comprehensive biostatistics services including sample size calculations, statistical analysis plans, and regulatory consulting.
Data Management
Clinical data management services including protocol development, e-CRF/e-PRO design, database setup and validation, data cleaning, coding, and locking.
Medical Writing
Comprehensive medical writing services providing a full range of medical documents required for clinical programs, produced in accordance with ICH guidelines.
Study Management
Broad range of solutions and tools to manage clinical research projects.
Clinical Operations Support
CPMs, CRAs, and CTAs providing tailor-made services and functional services according to client needs.
Regulatory Affairs Support
Assistance with regulatory affairs provided by a highly-experienced and well-trained team.
Biostatistics
Comprehensive biostatistics services including sample size calculations, statistical analysis plans, and regulatory consulting.
Data Management
Clinical data management services including protocol development, e-CRF/e-PRO design, database setup and validation, data cleaning, coding, and locking.
Medical Writing
Comprehensive medical writing services providing a full range of medical documents required for clinical programs, produced in accordance with ICH guidelines.
Study Management
Broad range of solutions and tools to manage clinical research projects.
Clinical Operations Support
CPMs, CRAs, and CTAs providing tailor-made services and functional services according to client needs.
Regulatory Affairs Support
Assistance with regulatory affairs provided by a highly-experienced and well-trained team.
Services
Comprehensive clinical data management services covering protocol support, eCRF/ePRO design, database build and validation, data cleaning, medical coding, reporting, and archiving.
Statistical services for clinical trials including statistical analysis, programming and reporting (service listed on site).
Regulatory and scientific writing services including preparation of regulatory documents and scientific communications (service listed on site).
Project and study management services to coordinate clinical trial activities across vendors and sites (service listed on site).
Operational support for clinical trials including site interactions and operational oversight (service listed on site).
Regulatory support services to assist with submissions and compliance activities (service listed on site).
Comprehensive clinical data management services covering protocol support, eCRF/ePRO design, database build and validation, data cleaning, medical coding, reporting, and archiving.
Statistical services for clinical trials including statistical analysis, programming and reporting (service listed on site).
Regulatory and scientific writing services including preparation of regulatory documents and scientific communications (service listed on site).
Project and study management services to coordinate clinical trial activities across vendors and sites (service listed on site).
Operational support for clinical trials including site interactions and operational oversight (service listed on site).
Regulatory support services to assist with submissions and compliance activities (service listed on site).
Expertise Areas
- Clinical data management
- Biostatistics and statistical programming
- Regulatory compliance and data standards (CDISC, e-records requirements)
- Clinical operations and study management
Key Technologies
- Electronic Data Capture (EDC)
- Interactive Web Response Systems (IWRS)
- eCRF and ePRO design
- CDISC SDTM and CDASH standards