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The pharma industry uses Artwork Flow to…
e-sign and ensure 21 CFR compliance.
Get your pharma labels approved the first time!
Project tracking
Create label workflows for end-to-end labeling with complete visibility. Track projects, tasks, and timelines.
Task creation
Assign tasks with detailed checklists to make sure all the steps within a label design are completed.
Design
Connect with design integrations and scale designs for different pharma packaging sizes.
Compliance
Easily comply with pharma requirements such as FDA’s DSCSA, 21 CFR Part 11, EU’s Falsified Medicines Directive, and more.
Review
Reduce repackaging and recalls with online proofing tools, comments, markup tools, and more.
Artwork management
Role-based user access, custom share links, version control, and instant search capabilities for complete control over your digital library.
Centralized label repository:
- Store all your pharmaceutical packaging in one secure location, accessible to all.
- Say goodbye to version control issues and wasted time searching for files.
Automated approval workflows:
- Set up automated workflows and receive notifications at each stage.
- Eliminate bottlenecks and reduce manual errors with proofing tools.
Automated compliance:
- Stay up-to-date with regulatory requirements and industry standards.
- Say goodbye to version control issues and wasted time searching for files.
Pharma serialization refers to the process of assigning unique identifiers (such as serial numbers or codes) to individual saleable units of pharmaceutical packaging.
These identifiers are often encoded as barcodes or QR codes to track and trace each unit throughout the supply chain. They contain information about the product’s origin, batch number, and validity or expiration date.
By implementing serialization, pharmaceutical companies can combat counterfeiting, enhance traceability, and ensure regulatory compliance.
Frequently asked questions
The labeling requirements might vary depending on the type of drug or pharmaceutical product. Typically, labeling requirements for pharmaceuticals include providing clear information about the drug, such as its name, dosage, and usage instructions. It must also include warnings about potential side effects and proper storage instructions. Additionally, the label should display the expiration date and lot number for safety and traceability purposes.
Compliance in the pharmaceutical industry means following rules and regulations to ensure medicines are safe and effective. It involves meeting standards set by government agencies to guarantee quality and consistency. This includes proper labeling, manufacturing practices, and testing procedures. Having label compliance software is crucial for pharmaceutical companies to ensure compliance with ease, streamlining the process of adhering to regulatory requirements and minimizing errors. Essentially, it's about making sure medicines meet all the necessary requirements to protect patients' health.