Aomics GmbH
Aomics GmbH is a German-based clinical data science CRO dedicated to advancing clinical development through data-driven insights and innovative solutions. They offer comprehensive, cost-effective solutions in biostatistics, statistical programming, clinical data management, bioinformatics, and more, supporting pharmaceutical, biotech, and medical device companies globally. Their mission is to empower and accelerate clinical development, aiming to contribute to life-changing therapies and improved healthcare outcomes. They value respect, honesty, innovation, integrity, environmental responsibility, employee growth, and customer satisfaction.
Industries
Nr. of Employees
small (1-50)
Products
Multi-omics analytics platform for immune-oncology
Platform integrating single-cell and bulk multi-omics data for tumor microenvironment profiling, immune cell quantification, cell–cell communication inference, biomarker discovery and prediction of immune-related adverse events.
Multi-omics analytics platform for immune-oncology
Platform integrating single-cell and bulk multi-omics data for tumor microenvironment profiling, immune cell quantification, cell–cell communication inference, biomarker discovery and prediction of immune-related adverse events.
Services
Statistical design and analysis services for clinical trials, including study design, sample size calculation, interim and adaptive analyses, survival analysis, PK/PD modelling and biomarker validation.
Development and validation of analysis pipelines and programs to produce analysis datasets, tables, listings, figures, and SDTM/ADaM-compliant datasets for regulatory submission.
End-to-end data management services from CRF design and EDC setup to data cleaning, query management, coding, reconciliation, database lock and archiving.
Mapping and conversion to SDTM/ADaM, creation of define.xml, and preparation of reviewer guides to support regulatory electronic submissions.
Adverse event case processing, aggregate safety reporting, literature surveillance, database reconciliation and epidemiological assessments.
Preparation of protocols, clinical study reports, investigator brochures, database-lock narratives and aggregate regulatory reports to support submissions and publications.
Statistical design and analysis services for clinical trials, including study design, sample size calculation, interim and adaptive analyses, survival analysis, PK/PD modelling and biomarker validation.
Development and validation of analysis pipelines and programs to produce analysis datasets, tables, listings, figures, and SDTM/ADaM-compliant datasets for regulatory submission.
End-to-end data management services from CRF design and EDC setup to data cleaning, query management, coding, reconciliation, database lock and archiving.
Mapping and conversion to SDTM/ADaM, creation of define.xml, and preparation of reviewer guides to support regulatory electronic submissions.
Adverse event case processing, aggregate safety reporting, literature surveillance, database reconciliation and epidemiological assessments.
Preparation of protocols, clinical study reports, investigator brochures, database-lock narratives and aggregate regulatory reports to support submissions and publications.
Expertise Areas
- Clinical trial management
- Biostatistics and statistical analysis
- Statistical programming and automation
- Clinical data management and EDC operations
Key Technologies
- Statistical programming and scripting
- Electronic data capture (EDC) systems
- CDISC SDTM and ADaM data models
- Define.xml and electronic submission packaging
News & Updates
Introduction: Clinical research plays a pivotal role in bringing new drugs, medical devices, and therapies to market while ensuring the safety and well-being of patients. Two key regulatory frameworks, Good Clinical Practice (GCP) and Good Manufacturing Practice (GMP), are fundamental in maintaining the quality and integrity of clinical trials and the production of pharmaceutical products.
Clinical trials are the backbone of medical research, driving advancements in healthcare by testing the safety and efficacy of new treatments, interventions, and therapies. One of the critical decisions in designing a clinical trial is selecting the appropriate study design. The choice of study design can significantly impact the trial’s outcomes and the validity of the results.
Linkedin Unveiling the Vital Role of Statistical Analysis in Clinical Research Clinical research stands as a cornerstone in the advancement of medical science, contributing to the development of novel treatments, therapeutic strategies, and healthcare innovations. Amid the intricacies of research, one essential element holds the key to deciphering the nuances hidden within data: statistical analysis.
Linkedin Understanding the Critical Steps of Clinical Data Management Clinical data management plays a pivotal role in the successful execution of clinical trials, ensuring data accuracy, integrity, and compliance throughout the research process. From study initiation to study closure, each step is meticulously designed to collect, manage, and analyze data with precision. In this comprehensive
Linkedin Empowering Cancer Treatment: Immuno-Oncology’s Triumph Through Tumor Microenvironment In the quest to conquer cancer, a groundbreaking approach has emerged that capitalizes on the body’s own defenses. Immuno-oncology, a revolutionary field, harnesses the immune system’s potency to combat tumors. But how does it achieve this feat? The answer lies within the intricate web of the
Linkedin Empowering Precision Medicine: The Role of Immuno-Informatics in Healthcare In the era of personalized medicine, where treatments are tailored to individual patients, a dynamic fusion of immunology and informatics is shaping the landscape of healthcare. Welcome to the realm of immuno-informatics, a cutting-edge field that harnesses the power of data and technology to unlock
Introduction: Clinical research plays a pivotal role in bringing new drugs, medical devices, and therapies to market while ensuring the safety and well-being of patients. Two key regulatory frameworks, Good Clinical Practice (GCP) and Good Manufacturing Practice (GMP), are fundamental in maintaining the quality and integrity of clinical trials and the production of pharmaceutical products.
Clinical trials are the backbone of medical research, driving advancements in healthcare by testing the safety and efficacy of new treatments, interventions, and therapies. One of the critical decisions in designing a clinical trial is selecting the appropriate study design. The choice of study design can significantly impact the trial’s outcomes and the validity of the results.
Linkedin Unveiling the Vital Role of Statistical Analysis in Clinical Research Clinical research stands as a cornerstone in the advancement of medical science, contributing to the development of novel treatments, therapeutic strategies, and healthcare innovations. Amid the intricacies of research, one essential element holds the key to deciphering the nuances hidden within data: statistical analysis.
Linkedin Understanding the Critical Steps of Clinical Data Management Clinical data management plays a pivotal role in the successful execution of clinical trials, ensuring data accuracy, integrity, and compliance throughout the research process. From study initiation to study closure, each step is meticulously designed to collect, manage, and analyze data with precision. In this comprehensive
Linkedin Empowering Cancer Treatment: Immuno-Oncology’s Triumph Through Tumor Microenvironment In the quest to conquer cancer, a groundbreaking approach has emerged that capitalizes on the body’s own defenses. Immuno-oncology, a revolutionary field, harnesses the immune system’s potency to combat tumors. But how does it achieve this feat? The answer lies within the intricate web of the
Linkedin Empowering Precision Medicine: The Role of Immuno-Informatics in Healthcare In the era of personalized medicine, where treatments are tailored to individual patients, a dynamic fusion of immunology and informatics is shaping the landscape of healthcare. Welcome to the realm of immuno-informatics, a cutting-edge field that harnesses the power of data and technology to unlock