Kriger Research Group International
Kriger Clinical Research Organization (CRO) is dedicated to advancing medical science and improving patient care by bridging the gap between innovative medical research and real-world healthcare solutions. They partner with pharmaceutical, biotechnology, and medical device industries to drive clinical trials forward, offering comprehensive services including regulatory affairs management, clinical trial design and management, data management and biostatistics, patient recruitment and retention, clinical monitoring, quality assurance, pharmacovigilance, medical writing, market access and health economics, and consulting services. They also provide specialized training programs in clinical research roles to support professionals in the industry.
Industries
Nr. of Employees
medium (51-250)
Products
Clinical Research Professional Course (online)
A professional development course for clinical research roles delivered as a self-paced online program with live interactive sessions, practical projects and customizable SOP templates.
Clinical Research Professional Course (online)
A professional development course for clinical research roles delivered as a self-paced online program with live interactive sessions, practical projects and customizable SOP templates.
Services
Support for regulatory documentation preparation, submissions and ongoing regulatory interactions across stages of clinical development.
Protocol development, trial planning and operational management to execute clinical studies within timelines, budgets and regulatory standards.
Services for data collection, cleaning, validation and statistical analysis to produce validated datasets and study results.
Design and execution of strategies to identify, enroll and retain eligible participants for clinical trials.
Monitoring services to ensure protocol adherence, data quality and participant safety at study sites.
Audit and quality services to verify compliance with GCP, SOPs and applicable regulations across trial operations.
Support for regulatory documentation preparation, submissions and ongoing regulatory interactions across stages of clinical development.
Protocol development, trial planning and operational management to execute clinical studies within timelines, budgets and regulatory standards.
Services for data collection, cleaning, validation and statistical analysis to produce validated datasets and study results.
Design and execution of strategies to identify, enroll and retain eligible participants for clinical trials.
Monitoring services to ensure protocol adherence, data quality and participant safety at study sites.
Audit and quality services to verify compliance with GCP, SOPs and applicable regulations across trial operations.
Expertise Areas
- Clinical trial management
- Clinical monitoring and GCP compliance
- Clinical data management
- Biostatistics
Key Technologies
- ICH-GCP compliance frameworks
- Electronic case report forms (eCRF)
- Clinical data management systems
- Biostatistical analysis methods