Resource Hub

Explore our collection of valuable resources, incorporating the latest news, events, regulatory intelligence, and thought leadership.

Learn More

Regulatory Intelligence

Stay current with ever-changing regulations. Utilize our comprehensive references to stay abreast of regulatory changes across a spectrum of medical topics from health authorities across the globe.

Events

RAPS Euro Convergence 2025
PharmaSUG US Conference 2025
Outsourcing in Clinical Trials UK and Ireland 2025
World Drug Safety Congress Europe
View More

Let’s Build a Healthier
& Safer World, Together

Connect with ClinChoice to discover how we can support the
development and commercialization of your drug or device.

Get In Touch

Resources

Whitepaper

The EU Clinical Trials Regulation

This paper provides changes and updates to Clinical Trials Regulation in the EU as of December 2023.

Read More

Whitepaper

Safety Assessment of E-Cigarettes in the EU

This whitepaper outlines safety requirements and key considerations in exposure assessments, hazard identification and risk assessments for e-cigarettes…

Read More

Whitepaper

Safety Assessment of E-Cigarettes in the US

This whitepaper outlines safety and risk assessments as well as literature monitoring for e-cigarettes in the US.

Read More

Press Release

ClinChoice Partners with Anju to Simplify the…

Ft. Lauderdale, FL June 26, 2023 – Anju Software, a leading life science technologies provider, announced that ClinChoice…

Read More

Blog

Our one-of-a-kind FSP Capabilities

Functional Service Provider (FSP) models can enhance workflows while speeding up timelines and remaining cost-effective. ClinChoice has over…

Read More

Blog

First Time Into Medical Writing for Medical…

New Intern (NI): Hello, Senior Medical Writer – today’s my first day! I’m really excited to know the…

Read More

Press Release

ClinChoice Acquires CROMSOURCE, Expanding its Global Presence

Philadelphia, USA; Shanghai, China; and Verona, Italy. March 01, 2023 – ClinChoice Medical Development is pleased to announce…

Read More

eBook

Considerations for Combination Product Registrations in the…

Combination Products are medical products comprised of two or more differently regulated constituent parts. They have many types…

Read More

eBook

Gut Microbiota: A Disregarded Subject in Toxicological…

The microbiome is coevolved in humans and healthy individuals. The microbiome is said to be in the symbiosis…

Read More

Blog

EMA and US FDA requirements for non-clinical…

Pertaining to the radiodiagnostic agents, there are few changes in the non-clinical requirements between the EMA (European Medical…

Read More