Non-Clinical Policies (C)
C
- Child Safe Organisation
- Clinical Incident Management
- Clinical Manual Handling
- Clinical Research - Access to Electronic Healthcare Records for Inspection Purposes
- Clinical Research - Bio-Specimen Collection, Processing and Shipping
- Clinical Research - Clinical Trial Management System User Support and Downtime
- Clinical Research - Close-Out and Archiving
- Clinical Research - Consent To Participate in Human Research
- Clinical Research - Creating Certified Copies
- Clinical Research - Equipment and Supplies - Receipt and Storage
- Clinical Research - Equipment and Supplies - Maintenance and Calibration
- Clinical Research - Financial Management
- Clinical Research - Investigational Medicinal Product (IMP) Accountability
- Clinical Research - Investigational Medicinal Product (IMP) Destruction
- Clinical Research - Investigational Medicinal Product (IMP) Quarantine
- Clinical Research - Investigational Medicinal Product (IMP) Receipt and Storage
- Clinical Research - Investigational Medicinal Product (IMP) Temperature Monitoring
- Clinical Research - Participant Reimbursements
- Clinical Research - Personnel Qualifications and Training Records
- Clinical Research - Personnel Roles and Responsibilities
- Clinical Research - Record Keeping
- Clinical Research - Review of Medical Results
- Clinical Research - Statistical Design, Analysis and Reporting
- Clinical Research - Storage of Chemicals
- Clinical Research - Trial Master File
- Clinical Research - Use of Biological Safety Cabinet
- Clinical Research - Use of Centrifuges
- Clinical Research - Use of Dry Ice
- Clinical Research - Use of Electronic Signatures
- Clinical Research - Use of Fridges and Freezers
- Clinical Research - Use of Fume Hood(s)
- Clinical Research - Use of Interpreters
- Clinical Research - Use of Laboratory Facilities
- Clinical Research - Use of Liquid Nitrogen
- Clinical Skills Assessment Framework
- Clinical Support Administrator (CSA) Managers Guidelines
- Clinical Support Administrator (CSA) Training Manual - General Wards
- Clinical Trials - Investigator's Brochure
- Clinical Trials - Protocol
- Clinical Trials - Safety Reporting
- Clinical Trials - SCHN Sponsorship
- Code of Practice for the use of GCNC Data Collection and Research Participants - CHW
- Committee Development and Administration
- Company Representatives Visiting SCHN
- Compressed Air Isolation - Maintenance - CHW
- Conferences, Major Events and Functions - Service of Alcohol
- Consumer Feedback Management
- Corporate Records Management
- Credentialing and Defining the Scope of Practice