Innovision Bio
Kapsam uyumu, hedef pazar görüşmesi ve proje materyalleri için kontrollü yol dahil B2B ticari ve proje koordinasyonu.
Manufacturing & Quality
Featured on-site view: GuangLong manufacturing and R&D facility
B2B project coordination supported by entity-level quality documentation, reviewed for each relevant project.
Proje rolleri
Innovision Bio B2B görüşmesini koordine eder. Belgeler, tesis bağlamı ve izinler her kayıtta belirtilen tüzel kişiye aittir.
Kapsam uyumu, hedef pazar görüşmesi ve proje materyalleri için kontrollü yol dahil B2B ticari ve proje koordinasyonu.
Üretim ve Ar-Ge tesis bağlamı. Tesis veya üretimle ilgili her ifade belge sahibine ve belirtilen kapsama sınırlıdır.
Ayrı kayıtlı ticari kuruluş. Tıbbi cihaz faaliyet lisansı ürün kaydı veya üretim yetkisi değildir.
Selected on-site views supporting B2B project review.
Representative operational view for project context; no certificate, test result or product release claim is implied.
Representative research-work view. Project-specific scope and documentation are reviewed separately.
Representative facility team activity for project context.
Representative operational view. Specific manufacturing conditions and release criteria are confirmed per project.
These reviewed documents are held by separately registered Chinese entities supporting Innovision Bio projects. Holder, stated scope, validity and project relevance are assessed individually.
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 entityHolder: 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 entityHolder: 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 entityThese 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.
Share your target market and project scope so the relevant entity, documentation pathway and next discussion can be reviewed.
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