March 7, 2023
Schlafender Hase Team
Intensifying regulatory requirements leave no room for error when putting goods into patients and consumers’ hands. Yet in life sciences, one of the most strictly controlled industries, more than 50% of product recalls are caused by packaging errors
March 6, 2023
Schlafender Hase Team
Practical next steps for medical device manufacturers & distributors as regulators demand the digital delivery of customer-facing product information in place of paper inserts.
March 1, 2023
Schlafender Hase Team
If you are proofreading manually, you are aware of how time-consuming it is. We have all heard the saying “time is money”, and this is very true for Regulatory Affairs professionals. In this article, we'll be exploring proofreading in Regulatory Affairs, and 5 ways that RA depts. are wasting money by relying on manual proofreading.
January 31, 2023
Schlafender Hase Team
Regulators in the life sciences industry are making clear moves to connect patients, physicians and other stakeholders across the healthcare system by implementing e-labelling initiatives.
January 31, 2023
Schlafender Hase Team
Accurate barcodes on healthcare packaging and labeling are just as important as any other information. An incorrect barcode can lead to expensive misprints and recalls.
January 13, 2023
Schlafender Hase Team
Read the Benefits Booklet to learn how TVT has helped companies in Life Sciences decrease their employees' stress and ensured patient safety with an efficient proofreading workflow.
November 4, 2022
Schlafender Hase Team
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? Join us on November 10th as we explore the why and how of a digital proofreading workflow.
