What kind of service

can we offer you today?

Regulatory Writing & Consulting

Clinical Research

Regulatory Technology

Staffing & Strategic Sourcing

Training & Education

Our Mission

We provide healthcare innovators unparalleled regulatory consulting, writing and support services through customized collaboration, problem solving, and technical expertise.

Let us tell you more about our Clinical Evaluation Expertise

1500+ Medical Devices Evaluated
500+ Implantable Devices
500+ Class III Devices
and more

Our Clinical Operations team knows your science

600+ Scientific Publications
Hundreds of Clinical Trial Documents
and more

Want training to become a great CER writer?

Our CER Boot Camp will cover everything you need to know

Visit the Global Education Center

Podcasts
White Papers
Promotions
and more

Clinical Data Support Services

Accurate collection
Active monitoring
Correct analysis
Safe storage
and more

We're the go-to CRO for CMC experience and expertise

100+ INDs, Phase 1-4
Orphan Drug Designation Application Approvals
Breakthrough Therapy Designations Application Approvals
and more

Education Center

We Share the love and the knowledge.

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Blog

Our blog posts cover hot industry topics. Engage with us and let us know what you think! 

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White Papers

Designed to be educational, our white papers take a deep dive into important regulatory topics.
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Offers and Products

Check out our current offers and promotions to get a great deal on your next project!
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Free Webinars

Our webinars are a chance to share insights we’ve earned working with a range of  products and agencies.
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Podcast

Chasing Compliance, presented by Global Regulatory Writing & Consulting, is a podcast focused on regulatory strategy, achieving and maintaining regulatory compliance, and the influence of regulation on healthcare overall. 

“I wanted to offer my sincere and heartfelt thank you for your excellence.”

“Thank you and admiration for the incredible team you’ve assembled – this success is as much your success as it is our success!”

“We really couldn’t have done it without you, and certainly not within our extremely aggressive timelines!”

“Really wanted to give a shout out to all of you – I know some of this is completely thankless work, so I wanted you all to know how much I appreciate the efforts. The documents are really in fantastic shape. We’re making headway closing/ locking up at a fast clip, and it really is thanks to your organization, diligence, and utter setup of COMPANY for success in our final days leading up to publishing. So – thank you…!”

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The Global Perspective:

The Global Regulatory Blog

Designing a Preclinical Program for Your Medical Device

  By: Sharon McFadden, DVM (Vice President, Clinical Operations & Medical Affairs)   The prospect of designing a preclinical program can be daunting, particularly if there is no precedent for the data needed and relevant models.   Here are some items to...

Creating Clinical Trial Budgets – Tips & Tricks

  By: Sharon McFadden, DVM (Vice President, Clinical Operations & Medical Affairs)  Figuring out a proposed budget for clinical sites can be challenging: knowing how to construct and execute the financials are a pivotal piece of trial design. Here are some...

Choosing the Right Study Site

By: Linda Peterson (Vice President, Clinical Operations) and Sarah Schaul (Clinical Trials Manager, Clinical Operations) When choosing the best sites for a study, from the location of the sites to the country, there are many different factors that need to be...

      Yup, we're this excited

      about your project!

We provide healthcare innovators unparalleled research and clinical development support, regulatory consulting, and writing services through customized collaboration, problem solving, and technical expertise.

 

+01-253-243-6121

info@globalrwc.com

14900 Interurban Avenue South Suite 271, PMB 98 Tukwila, WA 98168