Introducing The Global Regulatory Writing and Consulting Blog

April 13, 2021 00:26:33
Introducing The Global Regulatory Writing and Consulting Blog
Chasing Compliance: The Global Regulatory Podcast
Introducing The Global Regulatory Writing and Consulting Blog

Apr 13 2021 | 00:26:33

/

Show Notes

We are excited to announce the launch of the official Global Regulatory and Consulting Blog. To celebrate the release of the first blog posts we are sharing a conversation Jamie had with two people heavily involved with getting the blog off the ground, Rebecca Lynch and Sarah Schaul. They discuss why Global wanted to start a blog, the core subject matter covered, and what we would like for individuals to get out of the blog. Rebecca, Sarah, and Jamie discuss how we plan to leverage Global’s extensive Chemistry Manufacturing and Controls (CMC), Clinical, and Medical Device expertise to create a new resource for professionals within and outside of regulatory affairs and strategy. They also discuss their favorite upcoming blog topics. The blog can be found at www.globalrwc.com/the-global-blog  and within the education center.   

2:25 – Why did Global start a blog?

4:30 – Details on blog post themes, length, and frequency

7:40 – Clinical Aspects of the GRWC Blog

12:10 – What can readers expect to get out of the blog

19:30 – Blog topics we are all excited about

Other Episodes

Episode 0

September 05, 2020 00:51:22
Episode Cover

Part 2 - Overview of Global's CER Internship and Stories of Entering Regulatory Writing with Jacob Hoffman and Juliet Peña

Listen

Episode 0

April 22, 2022 01:04:25
Episode Cover

All About ADDM - New Technology To Manage Regulatory Communication Projects and Analyze Regulatory Feedback

In this podcast we introduce one of Global’s latest ventures, the Global Regulatory Technology Operations (GRTO) team and discuss their newest applications, the Advanced...

Listen

Episode 0

October 07, 2020 00:44:44
Episode Cover

Marysa Mezzetti - Risk Documentation and MDR

Have you considered the impacts of the Medical Device Regulation (MDR) on your current risk documentation and management strategies? You may be wondering, what...

Listen