№ lp_1_2_69042
File format: docx
Character count: 9090
File size: 50 KB
This document outlines the procedures for controlling clinical research documents at the CRC, including document versioning, approval processes, and periodic reviews.
Year:
Not specified
Region / City:
Not specified
Subject:
Clinical Research, Document Control
Document Type:
Standard Operating Procedure
Organization / Institution:
CRC
Author:
Not specified
Target Audience:
Research Staff, Regulatory Coordinators, Investigators
Period of Validity:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Price: 8 / 10 USD
The file will be delivered to the email address provided at checkout within 12 hours.
The file will be delivered to the email address provided at checkout within 12 hours.
Don’t have cryptocurrency yet?
You can still complete your purchase in a few minutes:- Buy Crypto in a trusted app (Coinbase, Kraken, Cash App or any similar service).
- In the app, tap Send.
- Select network, paste our wallet address.
- Send the exact amount shown above.
The final amount may vary slightly depending on the payment method.
The file will be sent to the email address provided at checkout within 24 hours.
The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2015
Region / City:
CRC
Topic:
Clinical Trials, Corrective and Preventive Action
Document Type:
Standard Operating Procedure
Organization:
Clinical Research Center (CRC)
Author:
Not specified
Target Audience:
Clinical Research Personnel
Period of Validity:
Ongoing
Approval Date:
01/01/2015
Effective Date:
01/01/2015
Review/Revision Date:
06/01/2016
Year:
2015
Region / City:
Not specified
Subject:
Clinical Research Procedures
Document Type:
Standard Operating Procedure (SOP)
Organization / Institution:
Clinical Research Center (CRC)
Author:
Not specified
Target Audience:
Site staff involved in clinical trials
Period of validity:
Not specified
Approval Date:
01/01/2015
Effective Date:
06/01/2016
Revision History:
Ongoing, with revision dates
Source Documents:
Clinical trial records, CRFs, IRB approvals, training certificates
Sponsor:
Not specified
Keywords:
Site Initiation Visit, SOP, clinical trial, CRC
Year:
2026
Subject area:
Civil and Environmental Engineering
Document type:
Conference proceedings author guidelines
Organization:
American Society of Civil Engineers
Conference:
CRC 2026
Intended audience:
Conference paper authors
Publication type:
Conference proceedings
Page limit:
Maximum 10 pages
Submission requirements:
Original unpublished work
Copyright holder:
ASCE
Formatting standard:
ASCE Publications
Source type:
Academic publishing guidelines
Editorial policy:
Conference technical committee
Author responsibilities:
Presentation at conference, originality, permissions
Year:
2015
Region / City:
Wye River, Separation Creek
Theme:
Community Development, Resilient Recovery
Document Type:
Submission
Author:
CRC
Target Audience:
Emergency Management Victoria, Community Leaders, Policy Makers
Period of Validity:
Ongoing
Date of Approval:
Not specified
Date of Modifications:
Not specified
Year:
2015
Region / City:
Not specified
Topic:
Clinical Research, Monitoring, SOP
Document Type:
Standard Operating Procedure (SOP)
Organization / Institution:
CRC (Clinical Research Center)
Author:
Not specified
Target Audience:
Clinical research personnel, investigators, study monitors
Period of Validity:
Not specified
Approval Date:
01/01/2015
Effective Date:
01/01/2015
Revision Date:
06/01/2016
Year:
2015
Region / City:
USA
Topic:
Clinical Research, Informed Consent
Document Type:
Standard Operating Procedure
Organization / Institution:
University of South Florida (USF)
Author:
Not specified
Target Audience:
Principal Investigators, Key Research Personnel
Period of Validity:
Indefinite
Approval Date:
01/01/2015
Revision Date:
06/01/2016
Programs:
CRC (Rehabilitation Counseling), CMHC (Clinical Mental Health Counseling)
Courses:
CRMH 802 Practicum; CRMH 810 Internship
Institutional affiliation:
School of Medicine
Document type:
Academic program requirements
Subject:
Clinical education standards and student eligibility conditions
Scope:
Practicum and Internship clinical placements
Supervision requirements:
Weekly one-to-one and face-to-face supervision by qualified master’s-level or licensed professionals
Site requirements:
Pre-approved practicum or internship sites serving persons with disabilities
Compliance requirements:
OSHA Training; HIPAA Training; CPR certification; Tuberculosis Test; Hepatitis B series or waiver; Criminal background check; Drug tests and fingerprinting if required
Insurance requirement:
Personal health and accident insurance enrollment
Agreement requirement:
Signed Affiliation Agreement between the School of Medicine and the agency
Geographic limitation:
Within one hour travel time from the University
Accreditation requirement:
State or federal licensure or appropriate accreditation
Documentation system:
Certified Background profile upload
Review cycle:
Annual review for second year students before Fall semester
Restriction:
No dual capacity as employee and intern during clinical placement
Financial condition:
Paid stipend permitted if time-limited and compliant with university policies
Year:
2015
Region / City:
Florida
Theme:
Research, Human Subjects
Document Type:
Standard Operating Procedure
Organization / Institution:
University of South Florida (USF)
Note:
Author
Target Audience:
Researchers, Institutional Review Boards
Effective Date:
01/01/2015
Revision Date:
06/15/2016
Year:
2019
Region / City:
Bangladesh
Thematic Area:
Child Rights, Monitoring and Reporting
Document Type:
Terms of Reference
Organization:
Plan International Bangladesh
Author:
Plan International Bangladesh
Target Audience:
Consultants, project staff, stakeholders involved in child rights and governance
Period of Validity:
2015-2019
Approval Date:
June 2015
Amendment Date:
June 2019
Job Title:
Interim Principal Psychologist, Children’s Disability Network Team (Grade Code 3727)
Irish Title:
Eatramhach Síceolaí, Príomhaí Cliniciúil
Campaign Reference:
Not specified
Closing Date:
3rd October 2025
Proposed Interview Date(s):
To be confirmed
Contract Type:
Fixed term (initial 12 months, potential extension to 24 months)
Location:
CRC Clontarf
Organisation:
Central Remedial Clinic (CRC)
Service Area:
Children’s Disability Network Teams (CDNTs)
Reporting To:
Kaizen Lead, Kaizen Promotion Office
Operational Collaboration:
Children’s Disability Network Managers (CDNMs)
Purpose of Post:
Delivery and development of a high quality, integrated Psychology service within an interdisciplinary model in CDNTs
Governance Framework:
Implementation of WRC Agreement 260124
Key Responsibilities:
Clinical governance, clinical supervision, service development, workforce planning, budget management, policy contribution, interdisciplinary collaboration
Review Mechanism:
Subject to review against agreed KPIs and Service Priorities
Professional Regulation:
Practice in accordance with CORU requirements
Year:
2024
Region / City:
N/A
Topic:
Presentation Guidelines for CI & CRC Joint Conference 2024
Document Type:
Presentation Guidelines
Organization:
N/A
Author:
N/A
Target Audience:
Conference Presenters
Period of Validity:
March 10, 2024
Approval Date:
N/A
Date of Changes:
N/A
Project:
Excluded People’s Rights in Bangladesh (EPR)
Theme:
Strengthening Public Institutions (SPI)
Type of Document:
Terms of Reference (TOR)
Funding Agency:
Foreign, Commonwealth & Development Office
Implementing Organization:
Manusher Jonno Foundation
Implementing Period:
Since 2006 (organizational engagement)
Geographical Coverage:
111 Local Government Units under 21 Upazilas and 2 City Corporations in 14 districts, Bangladesh
Sector Focus:
Primary Health Care, Agriculture Extension (including fisheries and livestock), WASH, Social Security, Local Government Institution Services
Cross-Cutting Issue:
Right to Information (RTI)
Target Groups:
Excluded and marginalized communities, local government institutions, civil society organizations, duty bearers, policy makers
Methodology:
Quantitative and qualitative research including Citizen Report Card, focus group discussions, key informant interviews, case studies, literature review
Deliverables:
Inception report, draft report, final report with recommendations
Expected Duration:
Ten weeks for draft submission; fifteen days for final submission after feedback
Location of Implementing Organization:
Mirpur-2, Dhaka, Bangladesh
Year:
2010
Region / city:
Global
Subject:
Ultraviolet B exposure and colorectal cancer
Document type:
Research appendix
Organization:
Neuroepidemiology
Author:
Mohr S, Gorham E, Garland C, Grant W, Garland F
Target audience:
Researchers, healthcare professionals
Effective period:
2010
Approval date:
2010
Modification date:
Not specified
Year:
2020
Region:
United Kingdom
Subject:
Equestrian Competition Rules
Document Type:
Conditions of Entry
Organization:
BHS Riding Clubs
Target Audience:
Riders and competitors
Applicable Period:
2020 competition season
Safety Requirements:
PAS015 or equivalent helmet, BETA Level 3 body protector for Hunter Trials and Eventers Challenge
Health Guidelines:
Compliance with BRC COVID-19 protocols
Horse Age Requirement:
Minimum 4 years old
Entry Limit:
Maximum 3 jumping classes per horse per day
Liability:
Organizer not responsible for accidents or property damage
Objection Procedure:
Written submission with deposit within 15 minutes of incident
Endorsement:
Club reserves right to refuse admission and deduct administrative fees if event canceled
Animal Welfare:
Mandatory cleanup and supervision, stallion handling rules, control of dangerous horses, dogs on short lead
Behavioral Rules:
Proper conduct required; unruly persons may be removed and forfeit entry fees
Regulatory Compliance:
Adherence to all BHS rules for riding clubs
Rider Safety:
Protective gear mandatory, including body protector and helmet
Competition Guidelines:
Applicable to all BHS events under 2020 rules, including COVID-19 measures
Allergen/Health Advisory:
Do not attend if feeling unwell or if household/friends unwell
Clearance and Grounds Use:
Horses must walk outside warm-up or competition areas, competitors clear rubbish and manure
Organisation:
Te Kaunihera Manapou │ Paramedic Council
Country:
New Zealand
Document type:
Call for expressions of interest and application form
Sector:
Paramedicine regulation and professional competence oversight
Legal framework:
Health Practitioners Competence Assurance Act 2003 (HPCAA)
Committee:
Competence Review Committee (CRC)
Roles referenced:
CRC member; Professional Advisor (Kaitohutohu Ngaio)
Responsible office:
Office of the General Manager/Registrar
Contact person:
Jacquelyn Manley
Position of contact:
General Manager / Registrar (Kaiwhakahaere Matua / Kairēhita)
Eligibility:
Registered paramedics with a current practising certificate
Preferred applicants:
Paramedics identifying as tangata whenua (Māori)
Key competencies referenced:
knowledge of Te Tiriti o Waitangi, tikanga Māori, bicultural healthcare perspectives, evaluation of professional competence
Supporting documents required:
Curriculum vitae and short biography
Application method:
Email submission
Contact email:
[email protected]
Functions described:
assessment of paramedic competence, advisory support to registration processes, policy and procedure development, evaluation of registration applications and complaints
Committee composition:
Two registered paramedics with current practising certificates and one layperson
Confidentiality requirement:
Members must sign a confidentiality agreement and follow terms of reference
Cultural framework referenced:
Te Tiriti o Waitangi and Māori cultural perspectives in healthcare
Year:
2023
Region / City:
N/A
Topic:
Registration Service, Operational Choreography
Document Type:
Change Request
Organization:
MHHS Programme
Author:
N/A
Target Audience:
Programme Participants
Period of Validity:
N/A
Approval Date:
08/02/2023
Date of Changes:
N/A
Organization:
United Nations Development Programme
Country:
Kuwait
Document type:
Standard Operating Procedures
Subject area:
Project cycle management
Implementation modality:
National Implementation Modality with Country Office support
Strategic framework:
UNDP Strategic Plan 2014–2017
Programme framework:
Country Programme Document and Country Programme Action Plan 2015–2018
Responsible institution:
UNDP Kuwait Country Office
Government coordinating agency:
General Secretariat of the Supreme Council for Planning and Development
Scope:
UNDP programmes and projects implemented in Kuwait
Project phases covered:
Formulation, appraisal, implementation, monitoring, evaluation, extension and closure
Intended users:
UNDP staff and national implementing partners
Annexes included:
Capacity assessment checklist, project document template, risk logs template, quality assurance checklist
Year:
Contract Year No.
Supplier:
Legal Name of Supplier
Facility:
Name of Facility
Contract:
Contract Title / Contract ID
Contract Date:
Contract Date
Time Period:
From insert date To insert date
Contract Capacity (MW):
Contract Capacity
Planned Outages:
As specified per unit and month
Unplanned Outages:
Percentage per unit and month
Overall Availability:
Percentage per unit and month
Type of Document:
Prescribed Form – Annual Operating Plan
Audience:
Buyer and Contract Management
Source:
Independent submission under Section 14.3(b)(i) of the Contract
Note:
Year
Issuing authority:
Ministry for Primary Industries
Jurisdiction:
New Zealand
Legal basis:
Biosecurity Act 1993
Document type:
Operating manual
Facility type:
Transitional Facility for uncleared risk goods
Approval status:
Approved Transitional Facility
Regulatory standards referenced:
TFGEN (Standard for General Transitional Facilities for Uncleared Risk Goods)
Scope of activities:
Receipt, holding, processing, treatment and inspection of uncleared risk goods; inspection of imported containers
Responsible roles:
Transitional Facility Operator; Deputy Transitional Facility Operator; Accredited Person
Compliance requirements:
MPI inspection and verification audits; access for MPI Inspectors at any reasonable time
Version control:
Review and amendments record with dates and sections
Training requirements:
MPI-approved training and refresher training for operators and accredited persons
Operational areas covered:
Security, biosecurity equipment, inspections, record keeping, hygiene management, pest control, audits, contingency plans