Resource Hub

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

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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
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Resources

Blog

Going Beyond the Missing: An Approach to Handling Dropouts in Longitudinal Clinical Trials

In longitudinal clinical trials, missing data is a threat to scientific integrity. Whether due to patient dropouts, missed visits, or…

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Newsletter

Regulatory Newsletter Oct – Dec 2023

Learn about Regulatory updates from Q4 2023 in this newsletter by ClinChoice.

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Newsletter

Regulatory Intelligence of Cosmetics Jan – Dec…

Regulatory Intelligence of Cosmetics for January through December of 2023.

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Press Release

ClinChoice Acquires CSI, Expanding its Global Footprint…

Shanghai, China; Philadelphia, USA; and Singapore, January 12, 2024 – ClinChoice, a leading global Contract Research Organization (CRO),…

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Whitepaper

The EU Clinical Trials Regulation

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

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Newsletter

Regulatory Intelligence of Cosmetics Jul – Sep…

Regulatory Intelligence of Cosmetics for July through September of 2023.

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Blog

Custom-Made Medical Devices: Are You Complying With…

The world is progressing rapidly with advanced technologies and customization in almost every sector to meet human needs.…

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Blog

Project FrontRunner: Advantages in directing oncology therapy…

What is Project FrontRunner? Project FrontRunner is an Oncology Center of Excellence (OCE) initiative that encourages sponsors to…

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Blog

Informed Consent: Guidance for IRBs, Clinical Investigators…

In August of 2023, the Food and Drug Administration (FDA) released a final guidance document that serves to…

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Blog

New EU MDR compliance dates: Impact assessment…

MDR transition Regulation (EU) 2017/745 on medical devices (MDR) has replaced the dated Medical Device Directive 93/42/EEC (MDD)…

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