AICROS
AICROS is a global consortium of small to midsize Contract Research Organizations (CROs) that provide clinical research services for the pharmaceutical, biotech, and medical device industries. They combine local expertise with global reach to deliver tailored, high-quality clinical trial management solutions. Their mission is to facilitate efficient, compliant, and high-standard clinical trials worldwide, leveraging their extensive experience, local regulatory knowledge, and collaborative network.
Industries
Nr. of Employees
small (1-50)
Services
Preparation of clinical study protocols, investigational plans, clinical evaluation reports for medical devices, informed consent forms, investigator brochures, IMP dossiers and clinical study reports.
Feasibility studies, site selection, contract and finance management, on-site and remote monitoring (including risk-based), project management and training for CRAs and investigators.
Full regulatory support including dossier pre-submission assessment, competent authority and ethics committee submissions, marketing authorization application support and post-authorization services.
Comprehensive pharmacovigilance services with clinically oriented safety operations, 24/7 medical monitoring, local safety services and operation of compliant safety databases; EU Qualified Person for Pharmacovigilance available.
CRF setup, clinical database setup and validation, data cleaning, medical coding, statistical programming and data mapping (e.g., CDISC).
Biostatistical analysis (interim and final), sample size calculation, randomization services, centralized statistical monitoring and statistical consultancy including SAP preparation.
Preparation of clinical study protocols, investigational plans, clinical evaluation reports for medical devices, informed consent forms, investigator brochures, IMP dossiers and clinical study reports.
Feasibility studies, site selection, contract and finance management, on-site and remote monitoring (including risk-based), project management and training for CRAs and investigators.
Full regulatory support including dossier pre-submission assessment, competent authority and ethics committee submissions, marketing authorization application support and post-authorization services.
Comprehensive pharmacovigilance services with clinically oriented safety operations, 24/7 medical monitoring, local safety services and operation of compliant safety databases; EU Qualified Person for Pharmacovigilance available.
CRF setup, clinical database setup and validation, data cleaning, medical coding, statistical programming and data mapping (e.g., CDISC).
Biostatistical analysis (interim and final), sample size calculation, randomization services, centralized statistical monitoring and statistical consultancy including SAP preparation.
Expertise Areas
- Clinical trial management (Phase I–IV and non-interventional studies)
- Medical writing and regulatory dossier preparation
- Regulatory affairs and submissions
- Pharmacovigilance and safety management
Key Technologies
- Electronic case report forms (eCRF)
- Electronic trial master file (eTMF)
- Interactive web response systems (IWRS)
- E2B-compliant safety database
News & Updates
AICROS Welcomes Asymchem Clinical as Newest Associate Member
AICROS has announced the acceptance of Asymchem Clinical as its newest associate partner, expanding its global network of CROs dedicated to high-quality clinical research services.
Conducting Clinical Studies in Romania and Bulgaria
An overview of the advantages of conducting clinical trials in Romania and Bulgaria, including regulatory environment, quality of sites, recruitment rate, logistics, and cost-effectiveness.
Why Conducting Clinical studies in Spain?
Highlights the opportunities and advantages of conducting clinical trials in Spain, including high-quality research infrastructure, qualified workforce, and significant participation in European trials.
AICROS Celebrates 20 Years of Excellence in Clinical Research
AICROS commemorates two decades of providing tailored clinical research solutions through its network of regional CROs.
The Future of Clinical Trials: Trends and Innovations
An analysis of emerging trends and technological innovations shaping the future landscape of clinical research.
Regulatory Challenges in Global Clinical Trials
A discussion on navigating complex regulatory environments across different regions for multinational studies.
AICROS Welcomes Asymchem Clinical as Newest Associate Member
AICROS has announced the acceptance of Asymchem Clinical as its newest associate partner, expanding its global network of CROs dedicated to high-quality clinical research services.
Conducting Clinical Studies in Romania and Bulgaria
An overview of the advantages of conducting clinical trials in Romania and Bulgaria, including regulatory environment, quality of sites, recruitment rate, logistics, and cost-effectiveness.
Why Conducting Clinical studies in Spain?
Highlights the opportunities and advantages of conducting clinical trials in Spain, including high-quality research infrastructure, qualified workforce, and significant participation in European trials.
AICROS Celebrates 20 Years of Excellence in Clinical Research
AICROS commemorates two decades of providing tailored clinical research solutions through its network of regional CROs.
The Future of Clinical Trials: Trends and Innovations
An analysis of emerging trends and technological innovations shaping the future landscape of clinical research.
Regulatory Challenges in Global Clinical Trials
A discussion on navigating complex regulatory environments across different regions for multinational studies.