TVT Resources | Schlafender Hase

March 15, 2023

Schlafender Hase Team

What is Document Comparison Software For Regulatory Affairs?

The major players in the Pharma and Medical Devices industries have either adopted or are in the process of adopting a software for document comparison. Like other technologies, this too has been a slow adoption despite it’s proven time, money, and stress savings. The goal of this article is to explain how document comparison software can help and why it is an essential part of any Regulatory Affairs tech stack.

5 minutes read

What is Document Comparison Software For Regulatory Affairs?

March 13, 2023

Schlafender Hase Team

Azurity Pharmaceuticals Case Study – Effortless Comparison in Labeling and Promotional Review

Following an increase in the number of products after an acquisition, the labeling team at Azurity Pharmaceuticals encountered new challenges in their proofreading process. TVT was their chosen regulatory proofreading software.

3 minutes read

Azurity Pharmaceuticals Case Study – Effortless Comparison in Labeling and Promotional Review

March 7, 2023

Schlafender Hase Team

A Business Case for a Document Comparison Software: The Best Insurance Policy for Regulatory Affairs

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

< 1 minute read

A Business Case for a Document Comparison Software: The Best Insurance Policy for Regulatory Affairs

March 6, 2023

Schlafender Hase Team

E-Labelling: Practical Next Steps for Medical Device Manufacturers

Practical next steps for medical device manufacturers & distributors as regulators demand the digital delivery of customer-facing product information in place of paper inserts.

4 minutes read

E-Labelling: Practical Next Steps for Medical Device Manufacturers

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 2, 2023

Schlafender Hase Team

8 Ways RA can help get Products to Market Faster

Bringing a new drug to market is time-consuming and costly, and generally takes 10 years and costs over $1 billion. The smallest lapse in labeling and packaging can jeopardize even the most well-planned submission. A proofreading and comparison software can help you get there faster, safer.

5 minutes read

8 Ways RA can help get Products to Market Faster

March 1, 2023

Schlafender Hase Team

5 Ways You’re Wasting Time & Money in Regulatory Affairs

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.

5 minutes read

5 Ways You’re Wasting Time & Money in Regulatory Affairs

February 2, 2023

Schlafender Hase Team

13 Questions to Ask When Choosing Comparison Software

Settling on a text comparison solution that does not require you to change your existing processes can be a daunting task, but we are here to help! We’ve outlined 13 questions for you to ask before making your final choice.

4 minutes read

13 Questions to Ask When Choosing Comparison Software

February 1, 2023

Schlafender Hase Team

Events – Meet the Rabbit!

Join us at DIA’s Advertising and Promotion Regulatory Affairs Conference, February 23-24, 2023

6 minutes read

Events – Meet the Rabbit!

Join us at DIA’s Advertising and Promotion Regulatory Affairs Conference, February 23-24, 2023

January 31, 2023

Schlafender Hase Team

e-Labelling: The Road to Reduced Med Device Packaging

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.

< 1 minute read

e-Labelling: The Road to Reduced Med Device Packaging

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.