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The document provides updates and reflections on the importance of in-person and hybrid conferences for cancer registrars, focusing on recent and upcoming events, changes in reporting guidelines, and educational opportunities.
Year: 2022
Region / City: Minnesota
Topic: Cancer Registrars, Conferences, Cancer Registry Education
Document Type: Newsletter
Organization / Institution: Minnesota Cancer Registrars Association (MCRA)
Author: Jackie Halsey, CNMT, CTR
Target Audience: Cancer Registrars
Effective Period: Spring/Summer 2022
Approval Date: Not specified
Revision Date: Not specified
Price: 8 / 10 USD
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Guidance for supplementary information to the CTR Cover Letter
Year: 2023
Region / City: EU
Topic: Clinical trial regulations, platform trial design
Document type: Guidance
Organization / Institution: EU-PEARL consortium, ECRIN
Author: Sal Morello, Siard Houtzager, Cecile Spiertz, Sabina Hernandez Penna, Peter Mesenbrink, Tom Parke, Franz Koenig, Benjamin Hofner, Katharina Hees
Target audience: Regulatory agencies, clinical trial sponsors
Period of validity: April 2023
Approval date: April 2023
Date of changes: Not applicable
Notice of Funding Opportunity for CTR Non-Proliferation Programming, 2026–2027
Year: 2026
Region / Focus Areas: Western Hemisphere, East Asia and the Pacific, South and Central Asia, Europe and Eurasia, Middle East and North Africa, Africa
Topic: Non-Proliferation, Countering WMD, Security Assistance
Document Type: Funding Opportunity Announcement
Issuing Agency: U.S. Department of State, Office of Cooperative Threat Reduction
Opportunity Number: DFOP0017675
Application Deadline: 6 March 2026
Funding Amount: $110,000,000 (approximate total available)
Award Range: $250,000 – $10,000,000 per award
Number of Awards: 50 (anticipated)
Funding Instrument Types: Grant, Cooperative Agreement, Inter-Agency Agreement
Project Duration: 12–24 months depending on justification
Eligible Applicants: U.S. for-profit organizations, U.S.-based non-profits/NGOs, U.S.-based higher education institutions, foreign non-profits/NGOs, FFRDCs, PIOs, FPEs, foreign higher education institutions
Priority Objectives: Disrupt proliferation networks, advance nuclear and biological security, protect critical technologies, implement sanctions on Iran, support U.S. SMR deployment
Clinical Trials Documentation Requirements According to CTR Annex I (2025)
Year: 2025
Region: European Union / Belgium
Subject: Clinical trial submission and documentation
Document type: Regulatory guidance / annex
Issuing authority: Clinical Trials Coordination Group (CTCG)
Related legislation: EU Clinical Trials Regulation (CTR), ICH E6 GCP
Audience: Sponsors of clinical trials, investigators, ethics committees
Applicable period: From 01/01/2025 for new submissions
Update date: 20/11/2025
References: Eudralex Volume 10, Belgian law of 7 May 2017, EMA guidelines
NAACCR CTR Preparation and Review Webinar Series Preparation for 2023 CTR Exam Quiz on Session 7
Year: 2023
Region / City: Not specified
Topic: Cancer Committee Standards and Practices
Document Type: Webinar Quiz
Organization / Institution: NAACCR
Author: Not specified
Target Audience: Cancer care professionals, particularly those preparing for CTR Exam
Period of Validity: Not specified
Approval Date: Not specified
Modification Date: Not specified
Topics: Halsey CNMT CTR