The world's leading automated proofreading software
August 17, 2023
Schlafender Hase Team
A Short History of Regulatory Authorities
Regulatory authorities are crucial for the safety and efficacy of medicines and medical devices. And yet, achieving the high level of regulation we have today has been a long road – with lives saved and lost along the way.
- August 17, 2023
- By: Mike Baird
4 minutes read
A Short History of Regulatory Authorities
Regulatory authorities are crucial for the safety and efficacy of medicines and medical devices. And yet, achieving the high level of regulation we have today has been a long road – with lives saved and lost along the way.
August 17, 2023
Schlafender Hase Team
A Guide to Medical Device Labeling Requirements
Navigating complex labeling requirements for medical devices. Your guide to the fundamentals of regulation and compliance and how automated proofreading can minimize your labeling risks.
- August 17, 2023
- By: Vineed Ravindranath
4 minutes read
A Guide to Medical Device Labeling Requirements
Navigating complex labeling requirements for medical devices. Your guide to the fundamentals of regulation and compliance and how automated proofreading can minimize your labeling risks.
July 31, 2023
Schlafender Hase Team
Maximizing the benefits of e-labeling in Pharma and Med Device
With electronic labeling gaining momentum across healthcare markets, are you ready to maximize the benefits?
- July 31, 2023
- By: Philipp Thomas
4 minutes read
Maximizing the benefits of e-labeling in Pharma and Med Device
With electronic labeling gaining momentum across healthcare markets, are you ready to maximize the benefits?
July 31, 2023
Schlafender Hase Team
Artwork Approval Processes for Pharma & Med Device
Improving artwork design and artwork approval processes can save patient lives and enhance company viability.
- July 31, 2023
- By: Dean Halliday
5 minutes read
Artwork Approval Processes for Pharma & Med Device
Improving artwork design and artwork approval processes can save patient lives and enhance company viability.
June 28, 2023
Schlafender Hase Team
5 Ways a Proofreading Software will Keep your Regulatory Affairs Team Happy
Proofreading documents manually in regulatory affairs (RA) in the life sciences industry is stressful, high-risk and can lead to job dissatisfaction. The stakes are high – errors can harm patient health, result in product recalls, and damage brand and company reputations. Here’s how TVT, the proofreading software for regulatory affairs, can keep an RA team happy.
- June 28, 2023
- By: Vineed Ravindranath
2 minutes read
5 Ways a Proofreading Software will Keep your Regulatory Affairs Team Happy
Proofreading documents manually in regulatory affairs (RA) in the life sciences industry is stressful, high-risk and can lead to job dissatisfaction. The stakes are high – errors can harm patient health, result in product recalls, and damage brand and company reputations. Here’s how TVT, the proofreading software for regulatory affairs, can keep an RA team happy.
June 21, 2023
Schlafender Hase Team
Why Spelling Errors Can Be Lethal in Medical Packaging
Spelling errors, missing information and language mistakes can lead to medical errors that put patient health at risk. Additionally, such errors can result in misprints, CAPA’s and product recalls.
- June 21, 2023
- By: Katarina Kresankova
4 minutes read
Why Spelling Errors Can Be Lethal in Medical Packaging
Spelling errors, missing information and language mistakes can lead to medical errors that put patient health at risk. Additionally, such errors can result in misprints, CAPA’s and product recalls.
May 26, 2023
Schlafender Hase Team
How to Reduce Drug Labeling Errors in Pharma
FDA (US), EMA (EU), ANSM (France), CFDA (China), BfArM (Germany) – just to name a few of the national and international bodies that regulate the pharmaceutical industry. They share a common purpose: to ensure the patient safety and efficacy of medicines. And for this, they have regulatory procedures.
- May 26, 2023
- By: Katarina Kresankova
3 minutes read
How to Reduce Drug Labeling Errors in Pharma
FDA (US), EMA (EU), ANSM (France), CFDA (China), BfArM (Germany) – just to name a few of the national and international bodies that regulate the pharmaceutical industry. They share a common purpose: to ensure the patient safety and efficacy of medicines. And for this, they have regulatory procedures.
May 23, 2023
Schlafender Hase Team
Regulatory Guidelines for Labeling in Pharma
Pharmaceutical labeling is a critical element of healthcare products and services that are strictly regulated by health authorities. This includes the Food and Drug Administration (FDA) in the United States and the European Medicines Agency (EMA) in Europe. The FDA oversees the safety and efficacy of pharmaceutical drugs, biopharmaceuticals, and other healthcare products. As a result, pharmaceutical labeling is a complex and meticulous process, with even minor errors resulting in significant consequences.
- May 23, 2023
- By: Peter Muller
4 minutes read
Regulatory Guidelines for Labeling in Pharma
Pharmaceutical labeling is a critical element of healthcare products and services that are strictly regulated by health authorities. This includes the Food and Drug Administration (FDA) in the United States and the European Medicines Agency (EMA) in Europe. The FDA oversees the safety and efficacy of pharmaceutical drugs, biopharmaceuticals, and other healthcare products. As a result, pharmaceutical labeling is a complex and meticulous process, with even minor errors resulting in significant consequences.
