TVT Resources | Schlafender Hase

September 23, 2024

Schlafender Hase Team

The Rise of Regulatory Requirements for Medical Devices

Peter Muller & Mike Baird of Schlafender Hase how well they think suppliers are adapting to new regulatory demands for Class 2 and 3 Medical Device Manufacturers.

4 minutes read

The Rise of Regulatory Requirements for Medical Devices

Peter Muller & Mike Baird of Schlafender Hase how well they think suppliers are adapting to new regulatory demands for Class 2 and 3 Medical Device Manufacturers.

September 23, 2024

Schlafender Hase Team

From Struggles to Solutions – Leveraging Technology for Faster Labeling Review in Crop Science

Across the Crop Science sector, both user and environmental safety are of highest priority. In this buyer’s guide, we will go over seven steps that will help you in your purchasing process, to ensure that you end up with the proofreading software you need.

< 1 minute read

From Struggles to Solutions – Leveraging Technology for Faster Labeling Review in Crop Science

September 23, 2024

Schlafender Hase Team

The booming medical device sector: How well are suppliers adapting to new regulatory demands?

4 minutes read

The booming medical device sector: How well are suppliers adapting to new regulatory demands?

September 9, 2024

Schlafender Hase Team

Rising regulatory demands: are medical device suppliers ready?

The global medical devices market is set to reach $886.80 billion in value by 2032 . As devices become more critical to patient outcomes, regulators’ quality and safety expectations and associated controls are increasing.

3 minutes read

Rising regulatory demands: are medical device suppliers ready?

September 2, 2024

Schlafender Hase Team

Avalis Publishing Case Study – Compliance through Watertight Version Control

Compliance, document integrity and a watertight version control process underpin all its publishing activities. Version control is a key factor as the two business partners deal with a large number of document updates and changes. Many of its clients do not have direct expertise in publishing the required regulatory documents.

3 minutes read

Avalis Publishing Case Study – Compliance through Watertight Version Control

September 2, 2024

Schlafender Hase Team

Soaring Medical Device Scrutiny: How is the Market Adapting?

4 minutes read

Soaring Medical Device Scrutiny: How is the Market Adapting?

August 22, 2024

Schlafender Hase Team

FHIR: Transforming Product Labeling

The shift from paper-based to digital processes has opened enormous opportunities in the healthcare sector in terms of data sharing and content management. But data can only be shared efficiently and add value if systems can "talk" to each other. The term we use for how compatibly systems work together is "interoperability." Traditionally, the healthcare sector has suffered from a high lack of interoperability.

6 minutes read

FHIR: Transforming Product Labeling

August 15, 2024

Schlafender Hase Team

Empowering Pharma and Regulatory Frameworks with Structured Content

Structured content ensures compliance in the pharmaceutical industry. Discover how FDA’s SPL and Canada’s SPM formats promote patient safety and efficiency.

5 minutes read

Empowering Pharma and Regulatory Frameworks with Structured Content

Structured content ensures compliance in the pharmaceutical industry. Discover how FDA’s SPL and Canada’s SPM formats promote patient safety and efficiency.

August 9, 2024

Schlafender Hase Team

The Importance of Structured Content in Product Labeling

In the first of a three-part series on structured content and structured product labeling, we explore why structured content is important, its benefits, and best practices for implementation.

4 minutes read

The Importance of Structured Content in Product Labeling

In the first of a three-part series on structured content and structured product labeling, we explore why structured content is important, its benefits, and best practices for implementation.