№ lp_1_12869
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Meeting minutes of the 2025 Field Trial Committee of the English Cocker Spaniel Club of America, detailing the planning for the 2025 National Championship and North American Championship events, including sponsorships, logistics, and new training requirements for judges.
Year:
2025
Region / City:
Eastern Region, Central Region, Western Region
Subject:
Field Trial Planning and Management
Document Type:
Meeting Minutes
Organization:
English Cocker Spaniel Club of America
Author:
Jack Glinsky, Jonathon Sims, Jeff Lusk, Barb Defalco, Paul McGagh, Mark Mercie, David Williams
Target Audience:
Members of the Field Trial Committee, Judges, Participants
Period of Effect:
2025
Approval Date:
July 15, 2025
Date of Changes:
Not specified
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Date:
August 3, 2011
Author:
Lisa Hull
Document type:
Personal letter
Subject:
Support for Anna Stubblefield
Institutions mentioned:
Rutgers University; Essex County Superior Court
Individuals mentioned:
Anna Stubblefield; DMan; Judge Siobhan Teare
Location:
Newark, New Jersey
Related event:
Criminal trial beginning September 9, 2011
Purpose:
Request for awareness, attendance, and support
Funding information:
Defense fund contribution details
Communication medium:
Written correspondence
Jurisdiction:
Australia
Regulatory framework:
Therapeutic Goods Administration (TGA) Clinical Trial Notification scheme
Document type:
Regulatory notification form
Scope:
Clinical trials involving medicines, biologicals, medical and therapeutic devices
Trial phases covered:
Phase I–IV, bioavailability/bioequivalence, device studies
Subjects:
Human participants
Ethics oversight:
Human Research Ethics Committee (HREC)
Approving authority:
Relevant institutional authority
Geographic coverage:
Australian trial sites with optional international sites
Responsible party:
Lead Investigator
Fee responsibility:
Lead Investigator
Related institution:
La Trobe University
Submission requirement:
Completed form and ethics approval
Note:
Year
Topic:
Clinical Trials
Document Type:
Plan
Target Audience:
Study team, sponsors, and regulatory authorities
Year:
2014
Region / City:
Geneva
Topic:
Revision of TGP/8, DUS Trial Design and Data Analysis
Document Type:
Draft Document
Organization / Institution:
International Union for the Protection of New Varieties of Plants (UPOV)
Author:
UPOV Office
Target Audience:
Technical Committees, Working Parties for Vegetables, Agricultural Crops, Fruit Crops, Ornamental Plants, and others involved in plant variety protection
Period of Validity:
Ongoing (as of 2014)
Approval Date:
May 27, 2014
Date of Changes:
N/A
Note:
Year
Year:
2025
Region / City:
Shanghai
Topic:
Arbitration, Early Determination
Document Type:
Guideline
Organization:
Shanghai International Economic and Trade Arbitration Commission (Shanghai International Arbitration Center)
Target Audience:
Parties involved in arbitration cases under SHIAC rules
Period of Validity:
Starting June 1, 2025
Approval Date:
June 1, 2025
Note:
Year
Topic:
Clinical Trial Agreement
Document Type:
Contract
Institution / Organization:
Istituto clinico Humanitas
Target Audience:
Medical, Scientific, and Research Professionals
Note:
Year
Topic:
Clinical Trials
Document Type:
Agreement Template
Organization:
Contract Research Organisation
Target Audience:
Sponsors, CROs, Clinical Trial Sites
Year:
2025
Region / City:
Lancaster, CA
Theme:
Herding Test and Trial
Document Type:
Event Announcement
Organization:
Antelope Valley Stockdog Club
Author:
Antelope Valley Stockdog Club
Target Audience:
Dog owners, participants in herding events
Period of Action:
14-16 March 2025
Approval Date:
N/A
Amendment Date:
N/A
Note:
Year
Type of Document:
Charter / Standard Operating Procedure
Study Phase:
Clinical Trial
Responsibilities:
Participant safety monitoring, data quality assessment, trial progress evaluation
Membership:
DSMB Chair, Voting Members, Independent Medical Monitor (if applicable)
Conflict of Interest Policy:
Disclosure and management of real or apparent conflicts
Meeting Requirements:
Quorum and attendance rules
Stopping Criteria:
Safety concerns and trial halting conditions
Year:
2024
Region / city:
South Sudan
Topic:
Procurement
Document Type:
Template
Organization / Institution:
South Sudan Public Procurement and Disposal of Assets Authority
Author:
South Sudan Public Procurement and Disposal of Assets Authority
Target Audience:
Procuring Entities (PEs), Bidders
Validity Period:
1 year (Trial Edition)
Approval Date:
November 2024
Date of Amendments:
None
Year:
2024
Country:
Canada
Study Type:
Phase II clinical trial
Treatment Regimen:
Bendamustine-Rituximab combination with concurrent Acalabrutinib
Participants:
62
Centers:
9
Primary Endpoint:
Combined Complete and Very Good Partial Response (CR+VGPR) rates
Secondary Endpoints:
Best overall response (BoR), progression-free survival (PFS), overall survival (OS), duration of response (DoR), Minimal Residual Disease (MRD)
Median Age:
69
Mutation Analysis:
MYD88 89.3%, CXCR4 28.6%, TP53 1.8%
Adverse Events:
Treatment-related adverse events (TRAEs) in 53 participants, 42 Grade 3/4 during combination therapy, 15 Grade 3/4 during monotherapy
Follow-up:
Median 350 days
Data Cut-off:
June 5, 2024
Document Type:
Clinical trial report
Year:
2024
Region / City:
Gauteng / Pretoria / Johannesburg
Subject:
Legal Procedure
Document Type:
Trial Practice Note Template
Organization / Institution:
High Court of South Africa
Author:
Not specified
Target Audience:
Legal professionals, Plaintiffs, Defendants
Period of validity:
N/A
Approval Date:
N/A
Date of amendments:
N/A
Year:
2024
Region / City:
Singapore
Topic:
Family Law, Court Procedures
Document Type:
Legal Form
Organization:
Family Court
Author:
Family Justice Courts
Target Audience:
Legal practitioners, applicants, respondents involved in family dissolution matters
Effective Period:
2024
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2023
Organization:
Colorado Department of Transportation (CDOT)
Document type:
Materials Bulletin
Audience:
Project personnel on CDOT Federal-Aid projects
Effective date:
November 10, 2022
Reference documents:
2023 CDOT Field Materials Manual, Materials Bulletin dated November 10, 2022, Materials Bulletin dated September 20, 2022
Regulation:
Infrastructure Investment and Jobs Act, Build America, Buy America Act
Forms:
CDOT Form 1600 – Contractor’s Certificate of Compliance
Materials covered:
Eligible construction materials including non-ferrous metals, plastics, glass, lumber, drywall, and manufactured products with steel or iron content ≥90%
Purpose:
Update project personnel on Buy America compliance requirements and CDOT procedures for certified construction materials
Note:
Job Title
Year:
2023
Region / City:
Wisconsin
Theme:
Field welding, inspection, and procedures for pile splices and field welded components
Document Type:
Checklist
Organization / Institution:
Wisconsin Department of Transportation (DOT)
Author:
Bill Hardy, CWI; Ryan Janssen, CWI
Target Audience:
Contractors, engineers, and welding inspectors
Effective Period:
Current year
Approval Date:
N/A
Modification Date:
N/A
Year:
2025
Region / city:
São Paulo
Topic:
Aero engines, industrial gas turbines, maintenance services
Document type:
Press release
Organization / institution:
MTU Maintenance do Brasil
Author:
Saša Lakić
Target audience:
Industry professionals, stakeholders in aerospace and turbine industries
Effective date:
October 9, 2025
Date of changes:
N/A
Document type:
Field safety plan guidelines
Institution:
University of Victoria
Governing policy:
Off-Campus Travel Risk Management Policy
Responsible units:
OHSE; Risk Management; Office of Research Services
Applicable activities:
Fieldwork; field schools; remote off-campus activities; research travel
Geographic scope:
Off-campus locations including remote areas
Approval authorities:
Academic Supervisor; Chair or Director; Dean
Review requirements:
OHSE and Risk Management review
Submission contact:
[email protected]
Associated forms:
Field Safety Standard Form; Special Authorization form; Off-Campus Activity & Travel Safety Plan (Low Risk)
Target audience:
Faculty; staff; students; trip organizers; academic supervisors
Safety focus:
Risk identification; emergency procedures; participant communications
Administrative purpose:
Planning; approval; record-keeping