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  • Home
    • About Us
    • Careers
  • Services
    • Compliance Focused
      • Misalignment Exceptions Management (US DSCSA)
      • EU Alert Management
      • Middle East Serialization Consulting
      • China Reporting Services
    • Business Operations Focused
      • Master Data Management
      • Trade Partner Onboarding
      • Level 4 System Validation
      • Serialization System Health Check
    • Business Processes Outsourcing
      • Managed Services CoE
      • US DSCSA Ti Digitization
  • Our Solutions
    • Traceware
    • nTrack
  • Clients
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    • Serialization
    • Digital
  • News
  • Contact
UK - Amendments to CDR(EU) 2016/161 to prevent supply disruptions

UK - Amendments to CDR(EU) 2016/161 to prevent supply disruptions

Jan 21, 2022 |

Introduction
Pharma Serialization - Roundup of 2021 & upcoming regulations of 2022!

Pharma Serialization - Roundup of 2021 & upcoming regulations of 2022!

Jan 7, 2022 | Serialization

The pharmaceutical industry like every industry has faced various challenges in the year 2021 which were closely related to the COVID-19 pandemic and its...
US DSCSA Serialization - 2023

US DSCSA Serialization - 2023

Dec 3, 2021 | Serialization

Introduction

5 steps to help you improve transparency in your supply chain

Nov 25, 2021 | Serialization

The plan you choose to improve transparency in your supply chain will depend on the risks in your business and what problems you wish to solve with the...
Medical Devices Regulations (MDR)

Medical Devices Regulations (MDR)

Nov 19, 2021 | Serialization, Pharmaceutical, Regulations, Compliance, Aggregation

Introduction
A complete guide to Brazil Serialization

A complete guide to Brazil Serialization

Nov 8, 2021 | Serialization, Pharmaceutical, Regulations, Compliance, Counterfeit

Understanding the difference between Serialization and Track & Trace

Understanding the difference between Serialization and Track & Trace

Oct 1, 2021 | Serialization, Pharmaceutical

Defining the basics
The need for automation

The need for automation

Sep 24, 2021 | Serialization, Pharmaceutical

Automation has revolutionized manufacturing by boosting production levels to meet increased demand in all industries.
SFDA Dossier requirements

SFDA Dossier requirements

Aug 27, 2021 | Serialization, Pharmaceutical, Regulations, Compliance

What you should know about SFDA classification and Drug registration

What you should know about SFDA classification and Drug registration

Aug 20, 2021 | Serialization, Regulations, Compliance, Aggregation

SFDA is the regulatory body in Saudi Arabia that handles the registrations and approvals for products that are distributed in Saudi Arabia whether they...
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    Recent Posts

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