Emergo by UL

Consultants for #MedDevice #regulatory compliance with a global presence. Follow up for fresh QA/RA news & updates!

[Emergo by UL @EmergoGroup]

Emergo by UL experts Frauke Schuurkamp and Lisanne de Vogel explain how human factors engineering can help assess meaningful differences between generic and brand-name products.

Read the article: https://t.co/fJOuO2m7S1

#HumanFactors

[Emergo by UL @EmergoGroup]

Manufacturers applying to register a #medicaldevice or #IVD with the Australian Register of Therapeutic Goods (ARTG) now have more options to leverage to fulfill the Manufacturer Evidence requirement to support an application. https://t.co/5vyWKTEIHV

[Emergo by UL @EmergoGroup]

U.K. MHRA has launched a public consultation on potential changes to the medical device regulatory framework. Have your say before Jan. 5, 2025, to shape the future of medical device and IVD regulations. https://t.co/mZYdz5cI3f

[Emergo by UL @EmergoGroup]

We are thrilled to take part at #RAPS2024, which will be held in Long Beach, California, from Sept. 17-19. If you’re attending, the Emergo by UL team will be at booth #739, ready to tackle your toughest #regulatory challenges in the medical device sector.
https://t.co/JIfVZyKkDd

[Emergo by UL @EmergoGroup]

Join us live on July 30, 2024, from 9-9:45 a.m. CST for an enlightening session with Ken Pilgrim, our Quality Assurance/Regulatory Affairs manager, on optimizing a quality management system (QMS) for global medical device companies. https://t.co/l497RFuSdo

[Emergo by UL @EmergoGroup]

Discover efficient approaches to streamline human factors validation testing for medical devices.

#MedicalDevice #RegulatoryAffairs #RegulatoryInsight #HumanFactors #Validation #MedTech https://t.co/znOBMH8JWO

[Emergo by UL @EmergoGroup]

Emergo by UL’s human factors specialists discuss how to apply human factors engineering to medical products as a system.

#MedicalDevice #RegulatoryAffairs #RegulatoryInsight #HumanFactors #HealthTech #MedTech https://t.co/LEGNS50pnc

[Emergo by UL @EmergoGroup]

Join our Emergo by UL human factors team live on July 11th, 2024 from 10 – 10:45 AM EDT. Our research directors Strochlic and Andrea Dwyer will share insights on engaging with the U.S. Food and Drug Administration. https://t.co/w7OT3Uy34d

[Emergo by UL @EmergoGroup]

Medical device makers who want to access the Hong Kong market must comply with the latest regulatory requirements in this special administrative region of China.

Learn more here ⬇️ ⬇️ ⬇️ https://t.co/Wxppx5xWqz

[Emergo by UL @EmergoGroup]

This is the first in a series of regulatory updates on the labeling standard for medical devices, IVDs and pharmaceuticals in Mexico.

Read more here 👇 https://t.co/8bTQDm5T2S

[Emergo by UL @EmergoGroup]

Navigate the unique regulatory requirements for your target markets with Regulatory Affairs Management Suite (RAMS) Regulatory Reports. https://t.co/GTUuD3hDaw

[Emergo by UL @EmergoGroup]

Regulatory Intelligence offers insights into global regulatory systems for medical device and IVD device companies to help plan your market expansion strategy. Sign up for a complimentary account today to learn more. https://t.co/Y4b3sPLhuf

[Emergo by UL @EmergoGroup]

Keep track of regulatory changes and how they impact your registrations across multiple medical device markets with Regulatory Watch. Sign up for a complimentary account today. https://t.co/6BosdyclQ1

#medicaldevice #ivddevice #regulatoryapproval #regulatoryaffairs

[Emergo by UL @EmergoGroup]

Save time and stress when determining your product classification with Emergo by UL’s Regulatory Affairs Management Suite (RAMS). https://t.co/TolUxOEpJR

[Emergo by UL @EmergoGroup]

Create your regulatory documentation faster and minimize errors that delay approvals with Smart Builder. Sign up for a complimentary Regulatory Affairs Management Suite (RAMS) account today. https://t.co/DtLLqYG5Ws

#medicaldevice #ivddevice #regulatoryapproval

[Emergo by UL @EmergoGroup]

Simplify your work, avoid missed renewals, and save time with automated registration and certification tracking with Regulatory Affairs Management Suite (RAMS) Registration Tracker. Sign up for a complimentary account today. https://t.co/t72zUzf79r

#medicaldevice #ivddevice

[Emergo by UL @EmergoGroup]

Regulatory Affairs Management Suite (RAMS) is designed to help you better understand and manage the always-evolving landscape of medical device regulations, compliance and representation. Learn more and sign up for a complimentary account today. https://t.co/ncsnz51ZWC

[Emergo by UL @EmergoGroup]

Visualize your path to product registration with intuitive, high-level process charts from Emergo by UL. Download your first chart at no cost when you register for Regulatory Affairs Management Suite (RAMS). https://t.co/EcY6rDnrQM

#medicaldevice #ivddevice #regulatoryapproval

[Emergo by UL @EmergoGroup]

Navigate the unique regulatory requirements for your target markets with Regulatory Affairs Management Suite (RAMS) Regulatory Reports. https://t.co/vhstyMYe0v

[Emergo by UL @EmergoGroup]

Regulatory Intelligence offers insights into global regulatory systems for medical device and IVD device companies to help plan your market expansion strategy. Sign up for a complimentary account today to learn more. https://t.co/bcz75mk9XB