Seamless Access to Professional Clinical Data Management and Biostatistics Experts for Drug Development
At Aomics GmbH, we are focused on providing solutions on Clinical Biometrics. We provide cost-effective, comprehensive solutions for Pharmaceuticals, Biotech and CROs SMEs.
Professional, quick, cost-effective and 100% independent statistical programming
Our commitment to excellence shines through in every aspect of our Clinical Research Organization (CRO) services, and this includes our statistical programming. We take pride in offering efficient, cost-effective, and 100% independent CRO statistical programming solutions.
Our team of experts ensures that your data is handled with the utmost precision and care, delivering results in a timely and cost-efficient manner. With our 100% independent approach, you can trust that your statistical programming needs are met with complete objectivity and transparency. We prioritize your success, and our dedication to efficiency and cost-effectiveness is evident in the high-quality services we provide.
Save time, money, and hassles
We provide cost-effective, comprehensive biostatistics & statistical programming solutions
Experienced biostatisticians and programmers
We have highly experienced Biostatisticians with an average of 10 years of experience
Accessible quality solutions with SAS certified programmers
Independent statistical programmers operate redundantly, leading to results being cross-verified, ensuring double-checking for accuracy
How does this work?
Study Planning and Initiation
In this phase, we work with your team to collaboratively define study objectives, develop a detailed study protocol, secure regulatory approvals, select and initiate clinical trial sites, and ensure all preparations are in place to commence the study
Protocol Development & Study Execution
During this phase, we actively actively work with you to oversee data collection and monitoring for quality and compliance, provide ongoing project management, and ensure safety monitoring and reporting as the study progresses
Data Analysis and Reporting
Following data collection, we conduct statistical analyses, prepares comprehensive study reports, including clinical study reports (CSRs), and assists in regulatory submissions to present the study's findings to regulatory authorities for review and approval
We provide expert biostatistics and CDM services to support your clinical research and study requirements
Celebrate the strength of our partnership as a Clinical Research Organization (CRO) dedicated to serving you. We specialize in biostatistics and Clinical Data Management (CDM) services, tailoring our expertise to meet your unique research and study needs.
With our commitment to excellence, we’re here to empower your clinical projects, ensuring accurate data analysis and streamlined data management processes. Together, we’ll drive successful outcomes in your research endeavors.
- Clinical Study Design
- PK/PD Analysis and Modeling
- Interim Analysis
- Survival Analysis
- Adaptive Clinical Trial Analysis
- Bioequivalent Trial and Biosimilar Trial Analysis
- Biomarker Validation
- SDTM Conversion Programming & Validation
- Clinical Data Management
Disease areas we are focused on
- Oncology
- Cardiology
- Diabetes
- Haematology
- Neurology
- Gynecology
- Dentistry
- Dermatology
- Rare-disease
Aomics GmbH Biostatistics and Statistical Programming Services
Aomics is a premier Clinical Research Organization (CRO) specializing in delivering cutting-edge biostatistics and Clinical Data Management (CDM) solutions. With a proven track record of excellence, we are your trusted partner in the realm of clinical research. Our dedicated team of biostatisticians and CDM experts is committed to providing top-tier services that cater to the unique needs of your research projects.
At Aomics, we understand the critical role that data plays in the success of clinical trials. With our proficiency in biostatistics, we ensure the accurate analysis and interpretation of your study data, guiding you toward informed decisions and regulatory compliance. Our CDM services streamline data collection, processing, and reporting, enhancing the efficiency and reliability of your research processes.
Become our valued partner and embark on your clinical project journey with us.
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