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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.

CLINICAL STUDY DESIGN DEVELOPMENT

MEDICAL WRITING

STUDY DOCUMENTS TRANSLATION AND ADAPTATION​

START-UP ACTIVITIES

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

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.

IMPORT - EXPORT LICENSE OBTAIN

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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