Our unique consulting service provides a comprehensive analysis of your raw experimental data, encompassing a broad range of bio-experimental techniques including high-throughput bioassays, multi-parameter flow cytometry, animal experiments, and more.

We utilize state-of-the-art data analysis tools and methodologies to extract meaningful insights from your data, ensuring a thorough, critical and unbiased evaluation. Your final reports are interactive if you prefer a dashboard, secure, and confidential, providing you with access to the detailed data analysis and allowing you to share it with collaborators while maintaining the integrity of your research findings.

Our commitment to transparency and reproducibility ensures that your data is analyzed in a rigorous and reproducible manner through detailed logging and version control, fostering confidence in the validity of your research conclusions.

Navigate complex decisions with confidence with our due diligence service. We meticulously examine raw data, delving into every detail with forensic precision, and utilizing robust methodologies to ensure unbiased and truthful assessments.

We provide in-depth reports that clearly convey our findings, backed by transparent documentation of every step in the analysis. We uncover potential red flags and provide objective assessments of potential risks and opportunities.

Let us be your trusted partners in due diligence. With our careful examination and objective reporting, you can make informed decisions with confidence.

We provide a comprehensive support for developing strong input for non-clinical regulatory dossiers, encompassing a range of services from data analysis and interpretation, to report generation and regulatory guidance.

We utilize state-of-the-art data analysis tools and methodologies to extract meaningful insights from your non-clinical data, including pharmacokinetics (PK) analysis, pharmacodynamics (PD) analysis, toxicology studies, safety pharmacology studies, and biomarker analysis.

We also provide tailored regulatory guidance to ensure your non-clinical dossiers are compliant with regulatory guidelines and standards, for example, with the interpretation of ICH guidelines, identification of critical non-clinical data, and development of regulatory strategies.

Our commitment to providing strong input for non-clinical regulatory dossiers empowers you to:

• Enhance the quality and consistency of your non-clinical data submissions
• Gain confidence in your non-clinical data and its interpretation
• Demonstrate compliance with regulatory requirements and standards
• Strengthen your chances of regulatory approval for your investigational product

Whether you are developing a new drug, biologic, or medical device, we can help you effectively navigate the complexities of non-clinical regulatory dossiers and, with an experienced and professional critical sense, pave the way for successful regulatory submissions.

We provide comprehensive bioinformatics analysis of your (sc)RNA-Seq data, whether it is from your own experiments or public databases. We utilize a suite of advanced bioinformatics tools, cloud computing, and state of the art methods to extract meaningful insights from the data, including differential expression analysis, gene ontology enrichment analysis, and network analysis. We provide scripts and documentation to ensure that your analysis can be replicated.

We also offer expertise in vaccine design, utilizing cutting-edge bioinformatics approaches to analyze vaccine efficacy, identify potential targets for vaccine development, and predict the immune response to vaccines.

Whether you are conducting basic research or developing new therapeutic interventions, we can help you extract valuable insights from your data and make informed decisions about your research and future directions.

We offer expert biostatistical analysis of your experimental and clinical data, providing comprehensive reports that are appropriate, and easy to understand.

We are well-versed in the latest methods and techniques in machine learning, ensuring that your data is analyzed rigorously and in accordance with best practices in statistics. Your reports are tailored to your specific research questions and objectives, providing clear and concise interpretations of your findings.

We also prioritize accessibility, ensuring that your reports are written in a user-friendly manner that is accessible to researchers with varying levels of statistical expertise. Whether you are conducting basic research or biomarker discovery in clinical trials, we can help you extract valuable insights from your data and make informed decisions about your research and future directions.

Transform your research into impactful narratives with our comprehensive scientific writing service. We offer a seamless journey from data analysis to publication and presentation, providing expert guidance and execution every step of the way.

• Manuscript writing − We collaborate with you to refine your research question, develop a strong narrative arc, and craft your scientific article from A to Z, ensuring:
  • Compelling introduction and literature review to establish strong context and positioning for your research
  • Clear and replicable methodology, to detail your methods with precision and transparency
  • Rigorous results and visualizations, to present your findings effectively with clear data analysis and compelling visuals
  • Insightful discussion and future directions, to highlight potential avenues for future research
  • Tidy reference management, to ensure accuracy and adherence to formatting guidelines


• Poster and presentation design − By trusting us as your partners in your projects, you will get:
  • Technical and scientific expertise, seamlessly translating complex research into understandable and engaging presentations
  • Data-driven storytelling, using impactful visuals and graphics to effectively communicate your key findings
  • Business focus, tailoring presentations to specific audience needs and formats, including business settings
  • Professionalism and clarity, ensuring your presentations are visually appealing and professionally designed for maximum impact

Equip researchers and scientists with the technical proficiency to analyze complex biological datasets! This comprehensive training program covers:

• Data science expertise − Installation, utilization, and best practices for analyzing biological data using industry-standard software packages like Python and R, as well as cloud computing (Google Cloud Platform).
• Advanced bioinformatics and biostatistics techniques − In-depth exploration of methods for analyzing high-throughput assays (RNA-Seq, flow cytometry, cell-based assays, etc.), animal studies, and molecular biology experiments, leveraging bioinformatics and biostatistical principles.
• Real-world application focus − Hands-on instruction emphasizing the practical implementation of these tools and software for effective and reproducible biological research.

By empowering researchers and scientists with these valuable technical skills, this training program fosters a deeper understanding of biological data and facilitates efficient analysis for groundbreaking discoveries.

We provide expert guidance and support for your preclinical drug development journey. This includes:

• Pharmacology − Designing and executing IND-enabling studies, from initial strategy and CRO selection to data interpretation and regulatory submissions. We also help define your Target Product Profile (TPP) and Translational Science Plans (TSP) to guide your clinical goals.
• Safety − Early identification of potential safety risks associated with your drug target, using literature-based Target Safety Assessments, AI and tailored experimental strategies. We design and manage your nonclinical safety program, including GLP toxicology studies, and support interactions with regulatory agencies.

We bridge the gap between your preclinical research and clinical development, ensuring a robust and efficient path to success.