Manufacturing & Quality

Featured on-site view: GuangLong manufacturing and R&D facility

Built for
Project Review

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

Proje rolleri

Nitelikli bir proje için net roller

Innovision Bio B2B görüşmesini koordine eder. Belgeler, tesis bağlamı ve izinler her kayıtta belirtilen tüzel kişiye aittir.

Innovision Bio

Kapsam uyumu, hedef pazar görüşmesi ve proje materyalleri için kontrollü yol dahil B2B ticari ve proje koordinasyonu.

GuangLong

Üretim ve Ar-Ge tesis bağlamı. Tesis veya üretimle ilgili her ifade belge sahibine ve belirtilen kapsama sınırlıdır.

Chuangxinli

Ayrı kayıtlı ticari kuruluş. Tıbbi cihaz faaliyet lisansı ürün kaydı veya üretim yetkisi değildir.

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 proje görüşmesi başlatın

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

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