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Digitizing the Proofreading Workflow: A Game Changer for Professionals in Life Sciences

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Mike Baird
2 minutes read
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Digital transformation is all the rage these days, but what does that actually mean for professionals working with regulated content in Pharma and Med Device, and more importantly, what does it mean for you?

Watch the webinar below, as we explore the why and how of a digital proofreading workflow.

Overview

Many organizations have made huge efforts to digitize several aspects of their business, but why not proofreading? The traditional proofreading process (manual proofreading) uses up a tremendous amount of precious human hours. If a mistake in regulated content is not identified, it can have a huge impact on patient safety and treatment efficiency.

Proofreading of regulated content in the pharma and medical devices industry is usually the responsibility of the person using the content to produce other materials. However, this long and error-prone task is only a small (but vital) part of the job, and not what many professionals have been trained for. Even the most highly trained and skilled professional proofreader reaches their limits during a working day, and this is when errors can go unnoticed.

Learning Objectives
  • Why proofreading is important to anyone working with Regulated Content
  • Why adopting a digital proofreading workflow is essential to remain competitive
  • How to guarantee data integrity with a digital proofreading workflow
  • Steps to implement a digital proofreading workflow
Who Should Watch
  • Regulatory Affairs
  • Regulatory Operations
  • Marketing/Ad/Promo
  • Quality Assurance
Presenters

Mike-Baird-Schlafender-Hase

Mike Baird
Director of Product Management

Mike is the Director of Product Management for Schlafender Hase. He 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, labelling, pre-media and artwork management leaders in the pharmaceutical and medical device sectors.

Katarina Kresankova - web

Katarina Kresankova
Account Executive

Katarina is a sales professional with a Master of Arts focused in Translating and Interpreting. With a demonstrated history in business strategy and negotiation, she specializes in customer acquisition. She is also passionate about cooking, interior design and enjoys long runs.

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

Director of Product Management, Schlafender Hase

Mike is the Director of Product Management for Schlafender Hase.

Learn More

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Digital transformation is all the rage these days, but what does that actually mean for professionals working with regulated content in Pharma and Med Device, and more importantly, what does it mean for you?

Watch the webinar below, as we explore the why and how of a digital proofreading workflow.

Overview

Many organizations have made huge efforts to digitize several aspects of their business, but why not proofreading? The traditional proofreading process (manual proofreading) uses up a tremendous amount of precious human hours. If a mistake in regulated content is not identified, it can have a huge impact on patient safety and treatment efficiency.

Proofreading of regulated content in the pharma and medical devices industry is usually the responsibility of the person using the content to produce other materials. However, this long and error-prone task is only a small (but vital) part of the job, and not what many professionals have been trained for. Even the most highly trained and skilled professional proofreader reaches their limits during a working day, and this is when errors can go unnoticed.

Learning Objectives
  • Why proofreading is important to anyone working with Regulated Content
  • Why adopting a digital proofreading workflow is essential to remain competitive
  • How to guarantee data integrity with a digital proofreading workflow
  • Steps to implement a digital proofreading workflow
Who Should Watch
  • Regulatory Affairs
  • Regulatory Operations
  • Marketing/Ad/Promo
  • Quality Assurance
Presenters

Mike-Baird-Schlafender-Hase

Mike Baird
Director of Product Management

Mike is the Director of Product Management for Schlafender Hase. He 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, labelling, pre-media and artwork management leaders in the pharmaceutical and medical device sectors.

Katarina Kresankova - web

Katarina Kresankova
Account Executive

Katarina is a sales professional with a Master of Arts focused in Translating and Interpreting. With a demonstrated history in business strategy and negotiation, she specializes in customer acquisition. She is also passionate about cooking, interior design and enjoys long runs.

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

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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

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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.

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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

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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.