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Our services

At Viacrystal, we offer comprehensive, full-cycle CRO services designed to support every stage of your clinical trial journey. From study planning and regulatory submissions to site management, logistics, and data analysis — our team brings regional expertise, operational excellence, and a hands-on approach to help you run efficient, compliant, and patient-focused studies.

Study planning

We help you shape your trial from the start to ensure your study is feasible, clear, and ready for execution.

And more:

  • Clinical study design development

  • Medical writing

  • Study document translation and adaptation

Start-up activities

Our team handles all the early-stage setup to get your trial running smoothly

And more:

  • Site initiation

  • Investigator and site contracts negotiation

Regulatory & Ethics

We support you through complex regulatory landscapes to secure timely approvals.

  • Regulatory submissions

  • Ethics Committee expertise support

Operational support

Once the trial is underway, we ensure everything stays aligned.

  • Project management

  • Site management and coordination

  • Medical monitoring

  • Central image review

  • Patient reimbursement

Database operations

We manage your trial data with precision and care, ensuring your results are reliable and ready for analysis.

  • Clinical data management

  • Biostatistics

  • Statistical programming

Logistics

Our logistics services cover every detail, ensuring your materials arrive safely and on time.

And more:

  • Import/export license obtaining

  • Sample transportation

Build study business plan
that attracts Sponsors!

Preparing to secure funding for your trial?

​Our CEO and Strategic Consultant offer expert-level guidance to help you develop a compelling study business plan.

 

For a fixed fee, you’ll receive support on:

  • Budgeting

  • Project structure

  • Strategic positioning

  • Preliminary feasibility

  • Optimal study geography

  • Insights into local standard of care

Contact us

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