№ files_lp_3_process_9_23705
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Corporate press release announcing the launch of a cloud-based multi-site energy management platform and outlining its functions, technical infrastructure, regulatory context, and company background.
Date:
March 31, 2025
Place:
Zurich, Switzerland
Company:
ABB Ltd
Division:
Smart Buildings Division, Energy Distribution Business Line
Product:
ABB Ability™ InSite Energy Pro
Platform Type:
Cloud-based energy management platform
Technology Partner:
AWS
Related Standard:
ISO 50001
Event:
Hannover Fair (March 31 – April 4, Hall 15, Stand D76)
Industry Sector:
Energy management and electrification
Target Audience:
Building owners, developers, energy managers of multi-dwellings and mid-sized commercial properties
Contact:
[email protected]
Address:
Affolternstrasse 44, 8050 Zurich, Switzerland
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2024
Region / City:
Fort Lauderdale, Florida
Theme:
Hospitality, Tourism
Document Type:
Press Release
Organization:
Caribbean Hotel & Tourism Association (CHTA)
Author:
Not specified
Target Audience:
Industry professionals, Tourism stakeholders
Period of validity:
Not specified
Approval Date:
May 20, 2024
Date of Changes:
Not specified
Year:
2026
Country:
United States
City / Region:
Sunnyvale, California
Document Type:
Regulatory filing
Form Type:
SEC Form 4
Regulatory Authority:
U.S. Securities and Exchange Commission
Legal Basis:
Section 16(a) of the Securities Exchange Act of 1934; Section 30(h) of the Investment Company Act of 1940
Reporting Person:
Iman Jeddi
Position of Reporting Person:
SVP & GM da Vinci Platforms
Issuer:
Intuitive Surgical Inc
Ticker Symbol:
ISRG
Date of Earliest Transaction:
February 10, 2026
Type of Securities:
Common Stock; Restricted Stock Units (RSUs)
Transaction Codes:
M (exercise or conversion of derivative security); F (payment of tax withholding obligation)
Derivative Security:
Restricted Stock Units granted February 10, 2023
Vesting Schedule:
25% annually over four years beginning February 10, 2023
Filing Date:
February 10, 2026
Year:
2023
Region / City:
Logan, UT
Topic:
Eating Disorders, Anorexia Nervosa, Intuitive Eating
Document Type:
Research Study
Organization / Institution:
Utah State University, Avalon Hills Eating Disorder Specialists, Mindful Path Psychological Services
Authors:
Francesca M. Knudsen, Mercedes G. Woolley, Spencer D. Bradshaw, Tera Lensegrav-Benson, Benita Quakenbush, Michael P. Twohig
Target Audience:
Researchers, Clinicians, Mental Health Professionals
Date of Approval:
2023
Date of Revision:
N/A
Year:
2022
Note:
Region / City
Topic:
Data and Safety Monitoring, Clinical Trials, Study Reporting
Document Type:
Instruction Sheet, Report Template
Organization / Institution:
NIAMS
Target Audience:
Investigators, Study Team Members, Data Managers, Study Statisticians, Monitoring Body
Contextual Description:
Instruction sheet for preparing data and safety monitoring reports for multi-site clinical studies.
Year:
2020
Note:
Region / City
Topic:
Clinical Research
Document Type:
Guideline
Organization / Institution:
National Institute of Arthritis and Musculoskeletal and Skin Diseases
Target Audience:
Researchers, Clinical Trial Coordinators, Investigators
Form number:
CER-NGER-015
Version:
1.0
Date of issue:
7 January 2025
Jurisdiction:
Australia
Regulatory framework:
National Greenhouse and Energy Reporting Regulations 2008
Scheme:
National Greenhouse and Energy Reporting Scheme
Related mechanism:
Safeguard Mechanism
Type of document:
Regulatory nomination form
Issuing authority:
Clean Energy Regulator
Subject matter:
Nomination of multi-site cement production facilities
Eligible activities:
Cement production attributable to Portland cement clinker
Reporting period applicability:
Activities conducted on or after 1 July 2023
Approval deadline:
30 June of the relevant financial year
Submission methods:
Post and email
Target entities:
Operators of multi-site cement production businesses
Administrative purpose:
Facility nomination and variation of existing nominations
Year:
2023
Document Type:
GHG Project Plan Appendix
Organization:
American Carbon Registry (ACR)
Version:
1.1
Date Published:
2023-12-01
Scope:
Multi-Site GHG Projects
Project Approach:
Aggregated or Programmatic Development Approach (PDA)
Validation Status:
Subject to validation and public disclosure
Year:
2023
Document type:
Pre-audit checklist
Program:
Chain of Custody certification
Standard referenced:
MSC Chain of Custody Standard: Default Version
Related standard:
ASC Chain of Custody Standard
Issuing organization:
Marine Stewardship Council
Copyright holder:
Marine Stewardship Council
Version:
2.1
Official language:
English
Intended users:
Single-site and multi-site organisations handling certified seafood
Certification scope:
MSC and ASC certified seafood products
Content focus:
Purchasing, identification, segregation, labelling, and promotion of certified products
Status:
Guidance document
Publication source:
MSC website
Year:
2020
Note:
Region / City
Topic:
Clinical Trials, Closeout Procedures
Document Type:
Procedure Guidelines
Organization / Institution:
NIAMS
Target Audience:
Researchers, Clinical Trial Coordinators, IRB Members, Study Site Personnel
Document type:
Administrative form
Subject area:
Human subjects research oversight
Regulatory context:
Institutional Review Board reliance and authorization
Applicable research type:
Collaborative multi-site research involving human subjects
Institution:
Campbell University
Responsible office:
Campbell IRB Office
Jurisdiction:
United States
Intended use:
Notification and coordination of IRB oversight
Related process:
IRB application and reliance agreement determination
Form status:
Not an IRB application
Source type:
Institutional administrative record
Year:
2017
Region / City:
United States
Topic:
Clinical Research, Multi-Site Clinical Trials
Document Type:
Manual, Guidelines
Organization / Institution:
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Author:
NIAMS
Target Audience:
Researchers, Clinical Trial Coordinators
Period of Action:
October 2017 and onwards
Approval Date:
October 2017
Date of Modifications:
Not specified
Year:
Not specified
Region / City:
United States
Topic:
Medical research protocols, ethics
Document type:
Protocol Addendum
Institution:
United States Army Medical Research and Development Command (USAMRDC)
Author:
Not specified
Target audience:
Research institutions, ethics committees
Validity period:
Not specified
Approval date:
Not specified
Amendment date:
Not specified
Year:
2026
Region / City:
Not specified
Subject:
Research Study Coordination and IRB Communication
Document Type:
Template / Protocol Guide
Institution:
Multiple participating institutions
Authors:
Not specified
Target Audience:
Research study teams, IRB personnel
Effective Period:
Duration of the study
Key Roles:
Reviewing IRB POC, Lead Study Team Representative, Relying Site POC, Relying Site Study Team Representative
Responsibilities:
Conflict of Interest management, study team training, local considerations, IRB application and review, consent form management, continuing review, reportable events, closure reports
Communication Channels:
Email, institutional portals, direct contact
Year:
Not specified
Region / City:
Not specified
Subject:
Human Research Protection, Institutional Review Board
Document Type:
Procedure
Organization / Institution:
Rutgers University
Author:
Not specified
Target Audience:
Principal Investigators, IRB Administrators, Reliance Administrators, External Institution Research Teams
Effective Period:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2025
Institution:
West Virginia University
Document type:
Investigator Manual
Scope:
Participating Site (pSite) responsibilities for Human Research under a single IRB
Audience:
Research investigators and study staff
Regulatory framework:
Federal human research protections and local institutional policies
Required training:
Human research protections training for all study personnel
Submission system:
WRAP SmartForms
Approvals:
sIRB approval and local institutional approvals
Responsible party:
Lead study team and pSite investigator
Key procedures:
Consent documentation, ongoing reporting, site-specific study management