Built for
Project Review

B2B project coordination supported by entity-level quality documentation, reviewed for each relevant project.

Discuss a B2B Project Review Project Context

프로젝트 역할

적격 프로젝트를 위한 명확한 역할

Innovision Bio는 B2B 논의를 조율합니다. 문서, 시설 맥락 및 허가는 각 기록에 명시된 법인에 귀속됩니다.

Innovision Bio

범위 정렬, 목표 시장 논의 및 프로젝트 자료의 통제 경로를 포함한 B2B 상업 및 프로젝트 조정.

GuangLong

제조 및 R&D 시설 맥락. 시설 또는 생산에 관한 모든 설명은 문서 보유자와 명시된 범위로 제한됩니다.

Chuangxinli

별도로 등록된 상업 법인입니다. 의료기기 영업 허가는 제품 등록이나 제조 허가가 아닙니다.

Facility context

Selected on-site views supporting B2B project review.

Laboratory quality work — 实验室质量工作

Representative operational view for project context; no certificate, test result or product release claim is implied.

Research activity

Representative research-work view. Project-specific scope and documentation are reviewed separately.

Sampling and review activity

Representative facility team activity for project context.

Filling-area operation

Representative operational view. Specific manufacturing conditions and release criteria are confirmed per project.

Entity-Level Qualifications

These reviewed documents are held by separately registered Chinese entities supporting Innovision Bio projects. Holder, stated scope, validity and project relevance are assessed individually.

ISO 9001

Holder: Qufu Guanglong Bioproduct Factory. ISO 9001:2015 certificate shown valid from 12 Feb 2024 to 11 Feb 2027; its documented scope is reviewed for the relevant project.

Affiliated manufacturing entity

Medical Device Business License

Holder: Qufu Chuangxinli Biotechnology Co., Ltd. Class III medical-device business licence shown valid from 9 Jan 2025 to 8 Jan 2030. It is a business-operation licence, not a manufacturing authorisation or product registration.

Affiliated trading entity

Cosmetics Production License

Holder: Qufu Guanglong Bioproduct Factory. Cosmetics production licence shown valid until 15 Nov 2026. Its documented scope does not approve an individual product or claim.

Affiliated manufacturing entity

These are entity-level documents, not product registrations, approvals or clinical evidence. Watermarked copies may be released only through the controlled-document process after holder authorisation and current-validity review.

B2B 프로젝트 상담 시작

Share your target market and project scope so the relevant entity, documentation pathway and next discussion can be reviewed.

문의하기