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Navigating DSCSA: Choosing a Compliance Approach for Dispensers
Review the different approaches healthcare organizations can take to achieve DSCSA compliance.
Saleable Returns Verification: What You Need to Know About Enforcement Discretion
See why companies should move ahead with a saleable returns solution even with FDA enforcement discretion.
Altran Q&A: Spain’s Small Pharmas Face Big Serialization Challenges for EU FMD
Understand the challenges small pharmas face as serialization approaches, and how industry expert Altran helps solve them.
India Regulatory Updates
View a compilation of the most recent track and trace regulations for the healthcare supply chain in India. Get insights into compliance updates.
Can My CMO Upload Product Data to the European Hub?
Learn whether or not contract manufacturing organizations can upload product data to the European Hub for pharma companies.
Clinical-Stage Pharmas: What Do You Need to Know About Serialization?
See why clinical-stage pharma companies must learn basic DSCSA serialization requirements—or risk years of work and millions of dollars.
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…
How Much Will Serialization Really Cost?
Get insights into how much serialization will really cost your company. Proven serialization solution providers can help identify additional costs.
Preparing for Russia Compliance: 6 Critical Considerations
Companies that sell product into Russia need to focus on six critical considerations, and understand how Russia challenges differ from those of FMD…
To Aggregate or Not: 5 Deciding Factors
Here are 5 questions to ask yourself when creating a strategy for serial number aggregation that will set you up for long-term success.
Russia Regulatory Updates
View a compilation of the most recent track and trace regulations for the healthcare supply chain in Russia. Get insights into compliance updates.
What are the Language Requirements for EU FMD Safety Features?
Discover what language the new unique identifier needs to be in on your medicine packs, depending on which European market you ship to.