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How are increased compliance requirements impacting medical devices?

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Peter Muller
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Join Peter Muller & Vineed Ravindranath for an engaging 15-minute LinkedIn Live session (previously recorded) where they explore the latest trends shaping the medical device sector! 

They dive into the top opportunities for innovation, the pressing challenges impacting the industry, and provide actionable tips to help you navigate regulatory compliance in this rapidly evolving landscape.

Learning Objectives:

  • Key trends and challenges in medical device compliance
  • Opportunities for innovation within evolving regulations
  • Strategic approaches to stay compliant in this dynamic industry

Watch the discussion on-demand: 

Presenters:

Peter Muller – Director Americas

For over 25 years, Peter Muller has worked on software and process improvement projects relating to proofreading with Fortune 500 companies from various industries: Pharmaceutical, Medical Device & Consumer Goods. He has a wealth of experience working with international clients to define their organization’s goals and help them leverage new technologies to achieve productivity gains, process improvements and cost savings.

Vineed Ravindranath – Account Executive

Vineed is an IT sales professional with over a decade of software solutions experience. He manages enterprise pharmaceutical and medical device manufacturers accounts that are located on or near the North American West Coast. He has also mastered 6 languages: Kannada, Tamil, Malayalam, Hindi, Telugu and English.

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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Peter Muller

Director - Americas at Schlafender Hase

For over 25 years, Peter Muller has worked on software and process improvement projects relating to proofreading with Fortune 500 companies from various industries: Pharmaceutical, Medical Device & Consumer Goods.

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Join Peter Muller & Vineed Ravindranath for an engaging 15-minute LinkedIn Live session (previously recorded) where they explore the latest trends shaping the medical device sector! 

They dive into the top opportunities for innovation, the pressing challenges impacting the industry, and provide actionable tips to help you navigate regulatory compliance in this rapidly evolving landscape.

Learning Objectives:

  • Key trends and challenges in medical device compliance
  • Opportunities for innovation within evolving regulations
  • Strategic approaches to stay compliant in this dynamic industry

Watch the discussion on-demand: 

Presenters:

Peter Muller – Director Americas

For over 25 years, Peter Muller has worked on software and process improvement projects relating to proofreading with Fortune 500 companies from various industries: Pharmaceutical, Medical Device & Consumer Goods. He has a wealth of experience working with international clients to define their organization’s goals and help them leverage new technologies to achieve productivity gains, process improvements and cost savings.

Vineed Ravindranath – Account Executive

Vineed is an IT sales professional with over a decade of software solutions experience. He manages enterprise pharmaceutical and medical device manufacturers accounts that are located on or near the North American West Coast. He has also mastered 6 languages: Kannada, Tamil, Malayalam, Hindi, Telugu and English.

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

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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.

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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.

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.

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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.