We offer data analytics, statistical analysis, clinical trial support, and research optimisation services. Our expertise spans genomic research, clinical trials, sector agnostic analytics, and manuscript preparation.
Yes. We regularly service clients throughout Europe, USA, and the Middle East, with experience navigating multiple regulatory frameworks.
We implement industry-leading security protocols and comply with international data protection regulations. All data transfers occur through secure channels, and we maintain strict confidentiality agreements.
Timelines vary by project scope. Statistical analyses typically take 2-4 weeks, clinical trial support can span several months, and manuscript editing usually requires 1-3 weeks.
Yes. We provide continuous support throughout project lifecycles, including regular updates, consultation calls, and post-delivery assistance.
All code, software, and deliverables developed during projects belong to our clients. We provide full documentation and transfer all rights upon project completion.
We strictly adhere to GDPR, HIPAA, and regional healthcare data regulations. Our team is trained in handling sensitive medical information with appropriate security measures.
Yes. We develop solutions that integrate with existing infrastructure and can optimise current workflows without disrupting operations.
Our team is proficient in R, Python, C++, and other languages required for data analysis and software development. We choose the most appropriate tools for each project.
We implement rigorous QC protocols including peer review, automated testing, and validation against industry standards. All deliverables undergo thorough quality assurance before release.
Yes. We can provide relevant case studies and testimonials from similar projects, subject to client confidentiality agreements.
We offer flexible payment structures based on project scope and duration. This typically includes milestone-based payments and can be discussed during project planning.