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1798 total results
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ANVISA: SNCM Expected to Start Immediately as a Priority Project
Integration with ANVISA's reporting system, SNCM, will be a critical focus for both domestic and multinational manufacturers in 2020.
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2-Minute Video: What You Need to Know About Brazil Compliance
In this video, TraceLink experts explain why Brazil may be your biggest compliance challenge.
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Horizontal Integration: Why It’s Essential for Brazil Compliance
Success in the Brazilian market will depend on horizontal integration: end-to-end data exchange between you and your trading partners. Learn why.
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Creating A Single Source of Truth for Your Global Inventory
Watch this video to learn how TraceLink’s integrated pharma supply chain platform can give you inventory visibility across your global markets.
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2019 Regulatory Update: Emerging Markets
See the latest regulatory developments in the Gulf Cooperation Council, Indonesia, Malaysia, and Africa from TraceLink’s Brian Daleiden.
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Leveraging Your Global Compliance Strategy in Saudi Arabia
TraceLink Director of Industry Marketing, Brian Daleiden, discusses how Saudi Arabia fits into a global compliance strategy for pharma supply chains.
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Orient Pharma and TraceLink: Partnering for Success on Serialization and Quality
Learn how TraceLink enables Orient Pharma to deliver serialization at a global scale.
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EMVO Approval: Certification vs. Conformance Tests
Learn about the updated process for being approved to send data to the EU Hub.
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Can You Afford a Manual Approach to EU FMD Compliance?
Manual data upload through the EMVO portal is simple in concept, but preparing and maintaining that data can be a challenge for smaller companies.
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Must-Know China Track and Trace Compliance Terms for the Pharmaceutical Supply Chain
The 2019 China Drug Administration Law introduced track and trace terms and agencies that you need to understand for your China compliance strategy.
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China eCode or GS1 Encoding? Weighing the Benefits and Risks
China eCode or GS1 Encoding: Which one is right for you? Watch this short webinar excerpt to understand key considerations for your China product strategy.
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China Reporting and Compliance Systems: Key Considerations
What makes China compliance so challenging? Watch this brief overview of China’s 3-tier reporting system to help guide your China serialization strategy.
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China Q&A: Preparing for New Reporting, Data, and Encoding Requirements
Learn how China’s National Medical Products Administration (NMPA) new reporting requirements and serialization options will affect pharmaceutical companies.
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Are Your Products China Ready? Three Key Decisions for Multinational Pharma Companies
China's drug administration law and serialization framework for medicines could affect your China product packaging strategy. Learn how today.
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Will My Current China Reports Work with the New Traceability Systems?
Learn how China’s amended Drug Administration Law expands the scope of NMPA reporting requirements and impacts your company’s serialization strategy.
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EDMC or GS1? 3 Keys to Choosing Your China Traceability System Provider
See what companies should consider when choosing between GS1 and EDMS encoding in China, and how that affects their choice of traceability system provider.
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German Biotech Chooses TraceLink Network Over Point-to-Point Approach
Learn why this pharma company opted for TraceLink's multi-tenant solution for compliance and automated validation.
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Small Italian CMO Sees Growth Opportunities with TraceLink
Learn why this contract manufacturing organization decided that choosing TraceLink for EU FMD was best for its business goals.
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Pharma Drops Vendor over Integration and Validation Failures, Joins TraceLink
One brand owner is now able to make up for lost time, maintain security, and move ahead in their mission to deliver quality and safety. Find out what prompted their switch to TraceLink.
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Compliance, Connectivity, and Customer References
Discover why 10 pharma companies and CMOs chose TraceLink over other providers—or switched after another provider let them down.
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Specialty Pharma Automates Validation to Ensure Compliant Launch
When a leading provider of CNS (central nervous system) drugs decided to launch its first independently commercialized product in the U.S., it selected the TraceLink Life Sciences Cloud as its serialization platform, and chose TraceLink’s Automated Validation Manager (AVM) to optimize its software testing and help address frequent updates in the regulatory landscape.
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Industry Poll: Russia Requirements are Most Complex of Any Market
Learn about Russia requirements for compliance.
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Will Serialization Affect Minimum Order Quantity for Rx Products?
Learn key definitions and requirements of how products are identified and sold under DSCSA, and how serialization can make product verification more accurate and efficient.
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Brazil Compliance: The Challenge of Horizontal Integration
Watch TraceLink General Manager Dan Walles explain why horizontal integration will be essential across Brazil's pharma supply chains.
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Four Reasons Why Pharma Companies Need a Serialization Intelligence Solution
Pharmaceutical companies need real-time visibility into operations, people, and systems across serialization infrastructures. See the reasons why.
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European Pharma Chooses TraceLink over ERP Provider for Compliance & Connectivity
Discover why a European pharma company selected TraceLink for EU FMD compliance rather than accept its ERP provider's proposal.
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Russia Update: 12 Nosologies Deadlines and Crypto Coding Confirmed
Read about two official Russian compliance declarations, including 12 Nosologies deadlines and crypto coding.
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Poll: Solution Provider Expertise, Platform Key to Saleable Returns
Learn how companies are trying to balance FDA saleable returns requirements, trading partner needs, and operational efficiency.
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Why Pharmacies and Hospitals Need to Think “Outside the Portal” for Serialization
What pharmacies are required to do to be ready for serialization and why they need to start developing a digital data strategy today.
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40 Key EU FMD Terms for Pharmacists
Learn the technical, legal, and industry terms you need to successfully prepare your hospital or pharmacy for EU FMD.
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