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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
  • Blog
    • Serialization
    • Digital
  • News
  • Contact
Preparing for the Final Stage of the US DSCSA

Preparing for the Final Stage of the US DSCSA

Jun 16, 2023 | Serialization, Pharmaceutical, Regulations, Compliance

The US Drug Supply Chain Security Act (DSCSA) is a federal regulation that aims to improve the safety and security of the pharmaceutical supply chain by...
Pharma Serialization requirements for Rwanda

Pharma Serialization requirements for Rwanda

Apr 21, 2023 | Serialization, Pharmaceutical, Master Data, Regulations, Compliance, Counterfeit, Aggregation

Key dates in Rwanda:
Australia TGO 106 serialization requirements

Australia TGO 106 serialization requirements

Jan 6, 2023 | Serialization, Pharmaceutical, Regulations

Key dates in Australia:
EU Medical Devices Regulations

EU Medical Devices Regulations

Oct 21, 2022 | Serialization, Pharmaceutical, Regulations, Compliance, Aggregation

Introduction
NHRA Bahrain Serialization Guideline for Pharma Companies

NHRA Bahrain Serialization Guideline for Pharma Companies

Apr 8, 2022 | Serialization, Pharmaceutical, Regulations, Compliance

Key dates in Bahrain
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

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...
The trending supply chain technologies in 2021

The trending supply chain technologies in 2021

Jul 30, 2021 | Serialization, Pharmaceutical, Regulations, Blockchain

The past decade has seen major breakthroughs in technology and though there have been really great strides, the pace of innovation in technology is still...
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    Recent Posts

    • Pharmaceutical Serialization in the GCC: Spotlight on Saudi Arabia
    • Pharmaceutical Serialization in Emerging Markets: A New Era of Global Compliance
    • China’s Push for Safer, Smarter Medicines: The Role of Drug Traceability Codes
    • Strengthening Global Health Supply Chains: USAID’s Approach to Enabling Traceability in Africa
    • Navigating Misalignment Exception Management Under DSCSA: Challenges and Solutions
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