Collection|Contact usWelcome,Shanghai DuanNa Enterprise Management Consulting Co., Ltd.!
Service phone021-59532958
ISO

Hot Keywords: ISO ISO9000 HACCP FACTORY

Why certification?

AUTHOR: http://wwww.shduanna.com.cn TIME: 2019-11-15 22:01:04

Why certifcation?

Security printing has changed dramatically during the past decades. New technologies have emerged.

Security features have grown in complexity to deter fraud and combat counterfeiting.

Yet some problems have grown larger, posing serious threats to both our industry and society as a whole –

forged identity and travel documents facilitating illegal border crossings, counterfeit currency passing into

worldwide circulation and false identities created from fake birth certificates, to name but a few.

Banknotes and identity documents are becoming ever more sophisticated, but so is counterfeiting. Security

printers and their suppliers cannot afford to stand still. Closing gaps and keeping ahead of the counterfeiters

on a global level remains a constant challenge.

Intergraf launched its certification scheme in 2003 as part of its mission to promote and protect the interests

of the printing industry. Together with technical experts from all over the world, it developed international

standards with one goal in mind: to provide security printers and their suppliers with a solid framework for

managing all security printing processes.

From logical security to physical security to supply chain assurance, Intergraf’s ISO 14298 and CWA 15374 ensure

that a set of requirements are met to guarantee a high level of security across all operations and processes,

eliminating risk for customers and their products.

Over 130 production sites in 50 countries across 5 continents are already reaping the benefits of Intergraf’s

certifications. And in doing so winning more business. Find out why you should be next.

 

 

 

 

 

NEWS

Training on the Clea...

1. Cleaning Validation Objectives and Regulatory Background   2. Core Definitions and Fundamental Principles   3. Cleaning Process Development (Four Elements, DHT/CHT) &nb...…
2026-9-5

Pharmaceutical GMP S...

Training Content Outline   Training Format: Approximately 32 hours of coursework + Case Studies   **Part 1: Audit Management under MAH System**   1. Audit Responsi...…
2026-9-4

FDA Audit Checklist...

Quality System and Data Integrity   Serial Number | Inspection Items and Requirements | Regulatory/Guideline Basis | Self-Inspection Results | Issue Description and Corrective Actions&n...…
2026-9-15

Purpose of FDA facto...

 Quality Management System Development and Operations: Oversee the establishment and optimization of the group headquarters' biopharmaceutical全产业链 quality management system, covering R&...…
2026-9-15

...

I. GMP Audit Regulatory Requirements  1.1 Interpretation of China’s *Regulations on Drug Inspection (Trial)*  ● **Inspection Types**:  - Licensing inspections (corresponding to *Dru...…
2026-9-15

Pharmaceutical GMP S...

I. GMP Audit Regulatory Requirements   II. Elements and Process of Self-Inspection and Audit   III. Key Points of Quality Management Assurance System Audit   IV. F...…
2026-9-11

Comparative Analysis...

I. Process Validation Regulatory Framework   Underlying Regulatory Basis   Core Principles   Phase Division   Batch Quantity Strategy   Reval...…
2026-9-11

NADCAP Certification...

思考完成(用时8秒) NADCAP Special Process Certification Guide   **I. Certification Overview**   NADCAP (National Aerospace and Defense Contractors Accreditation Program), initiated ...…
2026-8-2

Nadcap Certification...

Overview NADCAP (National Aerospace and Defense Contractors Accreditation Program) is a cooperative accreditation program jointly initiated by major U.S. aerospace and defense contractors...…
2026-8-2

What is intellectual...

What is intellectual property certification Intellectual property management system certification is to standardize intellectual property certification activities, improve its effectiv...…
2020-6-6

TEL

15000380587