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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
UAE TATMEEN - Pharmaceutical Drug Traceability

UAE TATMEEN - Pharmaceutical Drug Traceability

Nov 22, 2024 | Serialization, Pharmaceutical, Regulations, Compliance, Aggregation

The UAE Ministry of Health and Prevention issued Legislative Decree No. (73) of 2021 on June 14, 2021, regarding Pharmaceutical Products Traceability....
Pharma serialization requirements for Jordan

Pharma serialization requirements for Jordan

Nov 3, 2023 | Serialization, Pharmaceutical, Regulations, Compliance, Aggregation

Introduction
How to jump start serialization projects in pharma for new markets?

How to jump start serialization projects in pharma for new markets?

Oct 20, 2023 | Serialization, Pharmaceutical, Regulations, Counterfeit, Aggregation

Serialization projects in the pharmaceutical industry involve implementing a system that allows for the unique identification and tracking of individual...
Importance of Aggregation in Pharmaceutical Industries

Importance of Aggregation in Pharmaceutical Industries

Sep 22, 2023 | Serialization, Aggregation

Serialization has been a key focus of the pharmaceutical manufacturer for the past few years to comply with the global supply chain requirements to fight...
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:
EU Medical Devices Regulations

EU Medical Devices Regulations

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

Introduction
Medical Devices Regulations (MDR)

Medical Devices Regulations (MDR)

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

Introduction
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...
Saudi Pharmaceutical Serialization and Aggregation Roadmap for Vision 2030

Saudi Pharmaceutical Serialization and Aggregation Roadmap for Vision 2030

Jun 4, 2021 | Serialization, Pharmaceutical, Regulations, Compliance, Aggregation

Aggregation and its Importance to Pharmaceutical Companies

Apr 9, 2021 | Serialization, Pharmaceutical, Counterfeit, Aggregation

What is Aggregation? In short, aggregation is the undertaking of creating a hierarchic relationship between distinctive identifiers assigned to packaging...
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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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