Research efficiency and effectiveness can improve tremendously when you harness the power of advanced analytics.
We combine the right skills with the agility required to answer to the fast evolving demand. We support our clients in the transformation of raw data into meaningful and useful information and allow for the easy interpretation of these large volumes of data. We support our clients in interpreting datasets, merging them and ensuring consistency in the handling of multi-omics data sources.
Extracting information from large multidimensional datasets represents the next frontier of innovation and productivity. We provide data simulation and perform statistical analysis while mining large amount of data. Data simulation is a fundamental technique in statistical programming (R, SAS) and research. We bring together and develop the most useful algorithms for efficient data simulation in univariate and multivariate distributions.
We can help you leverage the value of existing data sources. We do so by developing ontologies, appropriate data models and by implementing relevant data processing tools. Our bioinformatics data curation services include bioinformatics ontologies such as Gene Ontology, ChEBI, etc. We also have ample know-how with loading large public datasets such as 1000 Genomes, TCGA, CCLE etc.
Bringing medical, pharmaceutical and biopharmaceutical products to market is a complex and high-risk race.
At Arrayo this is made possible by providing high calibre professionals to fill positions in all areas of clinical operations and clinical data science. Cooperation among a diverse group of stakeholders—including research sponsors, clinical investigators, patients, payers, physicians, and regulators—is necessary in conducting a clinical trial today. Each stakeholder offers a different set of tools to support the essential components of a clinical trial. Time, money, personnel, materials and a clear plan for completing the necessary steps in a trial are all part of the clinical research infrastructure, and all of those components require support systems, informatics and an experienced data science team. Our clinical data curation services include clinical ontologies such as ICD10, FHIR, etc..
On the operations side, we provide various services such as clinical trial management, CRO selection and finished clinical goods logistics.
We drive planning, outsourcing and day to day study oversight of operations to support clinical trial objectives. We develop of the overall clinical development plans and contingency/risk management plans. We can develop core clinical trial documentation and manage the Clinical Operations outsourcing strategy including RFP generation, negotiation, capabilities assessment, and selection.
We ensure compliance with SOPs, GCP and regulatory requirements for assigned clinical trials and development and review of SOPs and Clinical Operations systems. We provide oversight guidance of CROs to ensure that study timelines and goals are achieved and sites are monitored for compliance and quality control.
On the analytics side, we provide clinical data analysis, interpretation, and data representation for internal and external uses. We have expertise in statistical theory and development of statistical methodology. We use a set of tools including SAS, R, Oracle Clinical and Oracle RDC, and our consultants have an excellent understanding of the major regulatory guidances (ICH, FDA, EMA), electronic submission standards (SDTM, ADaM) and design of preclinical to post-marketing studies.