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

プロジェクト上の役割

適格プロジェクトの明確な役割分担

Innovision Bio は B2B の協議を調整します。文書、施設情報、許認可は各記録に記載された主体に帰属します。

Innovision Bio

範囲の調整、対象市場の協議、プロジェクト資料の管理経路を含む B2B 商務・プロジェクト調整。

GuangLong

製造・研究開発施設の背景情報。施設または製造に関する記述は、文書の名義人および記載範囲に限定されます。

Chuangxinli

独立して登記された商業主体です。医療機器の営業許可は、製品登録または製造許可ではありません。

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 プロジェクトの相談を始める

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

お問い合わせ