Seamless Access to Professional Clinical Data Analyst and Biostatistics Experts

At Aomics GmbH, we are focused on the analysis of healthcare data and clinical trials data. We provide cost-effective, comprehensive solutions for Pharmaceuticals, Biotech and CROs.

immune-oncology, clinical research organization (CRO), clinical trials, cancer, oncology, immunology, biomarkers, drug development, personalized medicine, adjuvant therapy, neoadjuvant therapy, immunotherapy, car t-cell therapy, immune checkpoint inhibitors (ICIs), targeted therapies, genomics, proteomics, bioinformatics, clinical data management (CDM), regulatory affairs, quality assurance (QA), medical writing, data analysis, Biostatistical consulting, Biostatistical services, Clinical data management
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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.

Disease areas we are focused on

Artificial intelligence & Machine Learning for Immuno-informatics

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.

Biostatistics consultation

Become our valued partner and embark on your clinical project journey with us.

Need Details of our services?

Download our Clinical Services BROCHURE

Something isn’t Clear?


Feel free to contact us, and we will be more than happy to answer all of your questions.