Home / Resources / Harmonization of Global Data: Bridging the Gaps Among Local Registries
WHITE PAPER

Harmonization of Global Data: Bridging the Gaps Among Local Registries

It’s no wonder data harmonization for global clinical trial disclosure is so difficult. There are at least 79 countries with clinical trial disclosure requirements, including 31 countries that follow European Union (EU) requirements. Forty countries have at least one clinical trial registry in addition to regional registries.

Citeline may contact you about relevant products, services, and content. To opt out of these communications or to manage what you receive, please visit our Preference Center.

Your information will be used in accordance with our Privacy notice.
Related products
Automated submissions to Clinical Trials
TrialScope Disclose
臨床試験情報開示の管理において最も広く信頼されているソリューション
Sponsors accessing TrialScope Intelligence for regulations and requirements.
TrialScope Intelligence
国際的な臨床試験情報開示のコンプライアンスに必要な重要な規制知識を一元化した対話型のリポジトリ
Regulatory compliance
Pink Sheet
製薬ニュースと規制トレンド分析のリーダー

Related resources

Hands with a digital icon for security hovering above them.
SEP 01, 2023
Whitepaper
薬事規制関連支援サービス

Clinical Trial Disclosure Compliance a Moving Target Due to Ever-changing Global Regulations

Gain insights on key factors driving disclosure rule updates and ways to minimize noncompliance risks.

Digital representation of the globe.
MAR 01, 2023
Whitepaper
薬事規制関連支援サービス

Global Clinical Trial Disclosure: What Noncompliance Penalties Are in Place, & How They Are Enforced

Industry groups and transparency advocates call for enforcing clinical trial disclosure noncompliance penalties. But are regulatory agencies doing so?

operationalizing-disclosure-intelligence-hero
NOV 01, 2023
Whitepaper
薬事規制関連支援サービス

Operationalizing Disclosure Intelligence for Go-to-Market Success

Comprehensive, proactive compliance management can help you operationalize disclosure intelligence — and establish your company as an industry leader.

View all resources