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The Role of Barcodes in Life Sciences, and the Key to Ensuring Barcode Accuracy

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Mike Baird
< 1 minute read
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Whether you are responsible for approving packaging, labeling or marketing assets, an incorrect barcode on your materials can lead to:

  • Lost Sales
  • Incorrectly scanned items or failures to scan
  • Expensive recalls
  • Damage to your Brand
Watch the 30-minute webinar where we dive into the who, what and where of barcodes.  
Key Learning Objectives
  • The fundamentals of barcode technology
  • Real-world applications of barcodes in pharma and med device
  • The importance of effectively managing digital barcodes
  • How to validate your digital barcode before going to print
Presenters
Mike Baird

Mike Baird – Director of Product Management at Schlafender Hase

Mike is committed to continuously improving the existing software portfolio and at the same time also delivering new and innovative solutions to exceed customer needs. He has more than 25 years of experience working with global packaging, labeling, pre-media and artwork management leaders in the pharmaceutical and medical device sectors.

Ensuring that the related risks of manual proofreading and approval processes are identified and solved quickly and easily, allowing only approved content to be printed or published.

Do you want to find out more about how your proofreading life can be easier? Get in touch and we’ll tell you all about it.

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Mike Baird profile picture

Mike Baird

Director of Product Management, Schlafender Hase

Mike is the Director of Product Management for Schlafender Hase.

Learn More

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Whether you are responsible for approving packaging, labeling or marketing assets, an incorrect barcode on your materials can lead to:

  • Lost Sales
  • Incorrectly scanned items or failures to scan
  • Expensive recalls
  • Damage to your Brand
Watch the 30-minute webinar where we dive into the who, what and where of barcodes.  
Key Learning Objectives
  • The fundamentals of barcode technology
  • Real-world applications of barcodes in pharma and med device
  • The importance of effectively managing digital barcodes
  • How to validate your digital barcode before going to print
Presenters
Mike Baird

Mike Baird – Director of Product Management at Schlafender Hase

Mike is committed to continuously improving the existing software portfolio and at the same time also delivering new and innovative solutions to exceed customer needs. He has more than 25 years of experience working with global packaging, labeling, pre-media and artwork management leaders in the pharmaceutical and medical device sectors.

Ensuring that the related risks of manual proofreading and approval processes are identified and solved quickly and easily, allowing only approved content to be printed or published.

Do you want to find out more about how your proofreading life can be easier? Get in touch and we’ll tell you all about it.

Subscribe to our blog

Past Webinars

November 19, 2024

Schlafender Hase Team

The Game-Changing Features of TVT 12: A New Era in Compliance and Efficiency

TVT 12 is here! This annual update is packed exclusively with new features and improvements from customer requests that support key industry initiatives, boost efficiency, and add even more speed and detail to your document reviews.

< 1 minute read

The Game-Changing Features of TVT 12: A New Era in Compliance and Efficiency

TVT 12 is here! This annual update is packed exclusively with new features and improvements from customer requests that support key industry initiatives, boost efficiency, and add even more speed and detail to your document reviews.

October 30, 2024

Schlafender Hase Team

How are increased compliance requirements impacting medical devices?

How are increased compliance requirements impacting medical devices? Discover the Future of Medical Device Regulation. We will dive into the rapid growth of the medical device sector, driven by cutting-edge technologies and rising regulatory requirements.

2 minutes read

How are increased compliance requirements impacting medical devices?

How are increased compliance requirements impacting medical devices? Discover the Future of Medical Device Regulation. We will dive into the rapid growth of the medical device sector, driven by cutting-edge technologies and rising regulatory requirements.

October 9, 2024

Schlafender Hase Team

Learning the New Language of the EMA & The FDA: FHIR

Watch our interactive discussion session focusing on the evolution and outlook of Fast Healthcare Interoperability Resources (FHIR). FHIR represents a significant step in how we manage and exchange information and is rapidly gaining acceptance. In this session, industry experts will provide an introduction to the FHIR initiative, explore some current applications as well as the impacts, benefits and prospective timelines.

2 minutes read

Learning the New Language of the EMA & The FDA: FHIR

Watch our interactive discussion session focusing on the evolution and outlook of Fast Healthcare Interoperability Resources (FHIR). FHIR represents a significant step in how we manage and exchange information and is rapidly gaining acceptance. In this session, industry experts will provide an introduction to the FHIR initiative, explore some current applications as well as the impacts, benefits and prospective timelines.