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.
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STUDY BUSINESS PLAN PREPARING
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​CONSULTING WITH EXPERTS
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​FEASIBILITY ASSESSMENT
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CLINICAL STUDY DESIGN DEVELOPMENT
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MEDICAL WRITING
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STUDY DOCUMENTS TRANSLATION AND ADAPTATION​
START-UP ACTIVITIES
Our team handles all the early-stage setup to get your trial running smoothly
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SITE INITIATION
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INVESTIGATOR MEETING ORGANIZATION
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TRIAL FILES PREPARATION (TMF, eTMF, ISF)
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INVESTIGATOR AND SITE CONTRACTS NEGOTIATION
REGULATORY & ETHICS
We support you through complex regulatory landscapes to secure timely approvals.
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REGULATORY SUBMISSIONS
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ETHICS COMMITTEE EXPERTISE SUPPORT
OPERATIONAL SUPPORT
Once the trial is underway, we ensure everything stays aligned.
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PROJECT MANAGEMENT
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SITE MANAGEMENT AND COORDINATION
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MEDICAL MONITORING
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CENTRAL IMAGE REVIEW
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PATIENT REIMBURSEMENT
DATABASE OPERATIONS
We manage your trial data with precision and care, ensuring your results are reliable and ready for analysis.
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CLINICAL DATA MANAGEMENT
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BIOSTATISTICS
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STATISTICAL PROGRAMMING
LOGISTICS
Our logistics services cover every detail, ensuring your materials arrive safely and on time.
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IMPORT - EXPORT LICENSE OBTAIN
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DEPOT SERVICES
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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:
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Budgeting
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Project structure
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Strategic positioning
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Preliminary feasibility
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Optimal study geography
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Insights into local standard of care