Introduction
The Center for Non-Clinical Trials is a specialized institution certified as a non-clinical contract research organization (CRO) holding AAALAC International accreditation. Unlike CROs that require medical staff for testing, our center provides objective and reliable non-clinical trial services tailored for medical devices, based on a professional system and experienced testing personnel. We ensure high quality by managing trial timelines, follow-up procedures, and result reporting. Above all, we maintain environmental conditions that far exceed the minimum standards required by regulatory authorities, securing the highest level of data credibility.
Non-Clinical Trial Support Procedure
STEP 01
Trial Request
- Submission of inquiry form via the website
- Consultation on trial content — on-site visit to the center or online consultation
- Trial plan drafting & personnel assignment — draft and review trial schedule, methodology, and result analysis plan
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STEP 02
Trial Contract
- Issuance of quotation based on trial content
- Contract drafting & signing, issue tax invoice
- Animal experiment plan submission & approval — IACUC approval process
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STEP 03
Trial Preparation
- Pre-trial meeting — discussion of detailed trial documents among assigned personnel
- Receipt of trial samples — receive and inspect trial samples
- Animal admission — quarantine and acclimatization prior to trial
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STEP 04
Trial Conduct
- Trial execution according to the pre-established schedule and protocol
- Result analysis — organize and analyze trial results and raw data
- Statistical analysis and validation of trial results
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STEP 05
Trial Completion
- Internal review of all trial analysis data
- Final report (draft) preparation and internal review by trial personnel
- Final report issuance to the client institution and approval completion