№ files_lp_4_process_1_51826
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Official amendment detailing corrections to line item 1 of the solicitation and specifying the technical and administrative requirements for the In Vivo Xtreme Imaging System and related laboratory equipment for live-animal research.
Year:
2014
Region / City:
Pittsburgh, PA, USA
Subject:
Government procurement of imaging and laboratory equipment
Document Type:
Contract amendment / solicitation modification
Issuing Agency:
U.S. Department of Veterans Affairs, Veterans Health Administration, Service Area Office East
Contractor:
Bruker Biospin Corp.
Contracting Officer:
Travis Gibbons
Effective Date:
25-Jul-2014
Solicitation Number:
VA268-14-Q-0031
Amendment Number:
1
Equipment Included:
In Vivo Xtreme Imaging System, Multimodal Animal Rotation System (MARS), Anesthesia System, Bone Density Software Module
Purpose:
Correct description of line item 1 and update price schedule
Key Features:
Fluorescence and bioluminescence imaging, multi-animal anesthesia, skeletal X-ray co-localization, high-resolution camera, software upgradability, PET/SPECT imaging, multi-angle imaging without handling animals
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2019
Location:
Bartlett, TN
Theme:
Swimming competition
Document Type:
Event schedule
Organizing Body:
Southeastern Swimming, Inc.
Author:
Bartlett XTREME Swimming Team
Target Audience:
Swimmers, coaches, and event officials
Period of Action:
December 7-8, 2019
Approval Date:
N/A
Modification Date:
N/A
Year:
2023
Region / City:
United States
Topic:
Education, Literacy Development, Reading Programs
Document Type:
Educational Program Description
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Adolescents, Educators, Literacy Specialists
Implementation Period:
Ongoing
Approval Date:
Not specified
Date of Last Revision:
Not specified
Jurisdiction:
Colorado, United States
Regulatory framework:
Colorado Revised Statutes (C.R.S.)
Statutory basis:
Sections 44-30-201, 44-30-302, 44-30-816, 44-30-818 C.R.S.
Rule number:
Rule 21
Amendment date:
August 14, 2016
Game covered:
Deuces Wild Xtreme
Game type:
Blackjack-poker combination table game
Deck composition:
53 cards (standard 52-card deck plus Joker)
Wild cards:
All Deuces and the Joker
Game objective:
Player achieves a higher-ranking five-card hand than the dealer
Game developer:
Galaxy Gaming, Las Vegas, Nevada
Authorized operators:
Retail gaming licensees
Wager types:
Ante, Odds, Play wager, and optional bonus wagers
Optional bonus wagers:
Bad Beat Xtreme, Trips Plus Wild, Goin’ Wild, Goin’ Wild Progressive, Too Wild Progressive, Five-Card Linked Progressive
Equipment requirement:
Approved gaming table with Deuces Wild Xtreme layout and signage
Payout structure:
Defined odds and bonus pay tables based on hand rankings
Year:
2024
Region / City:
Forest, ON
Theme:
Ringette Program
Document Type:
Program Overview
Organization:
Forest Xtreme Ringette
Author:
Forest Xtreme Ringette
Target Audience:
Parents and players of FUN1 and FUN2 ringette programs
Period of Action:
September 2024 - March 2025
Approval Date:
August 2024
Date of Changes:
N/A
Level:
FUN1, FUN2
Season Duration:
Starts after Labour Day, ends in March
Year:
2022
Region / City:
Not specified
Topic:
Bone health, flavonoids, sea buckthorn
Document Type:
Research Table
Institution:
Not specified
Author:
Not specified
Target Audience:
Researchers in pharmacology, bone health, and phytochemistry
Period of Action:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Note:
Contextual description
Year:
2022
Region / city:
Online
Topic:
SL LBT failure detection and recovery procedure
Document Type:
Draft
Organization / institution:
3GPP TSG-RAN WG2
Author:
vivo (Rapporteur)
Target audience:
Industry professionals, telecommunications companies
Effective period:
October 2022
Approval date:
Not specified
Date of changes:
Not specified
Title:
The ARRIVE reporting checklist
Related guideline:
ARRIVE guidelines 2.0
Subject:
Reporting standards for in vivo animal research
Document type:
Reporting checklist
Scope:
Articles describing in vivo animal experiments
Sections:
Essential 10; Recommended Set
Items:
21 main items with sub-items
Key topics:
Study design; Sample size; Inclusion and exclusion criteria; Randomisation; Blinding/Masking; Outcome measures; Statistical methods; Experimental animals; Experimental procedures; Results; Ethical statement; Housing and husbandry; Animal care and monitoring; Interpretation; Generalisability; Protocol registration; Data access; Declaration of interests
Cited work 1:
The ARRIVE guidelines 2.0: Updated guidelines for reporting animal research, PLOS Biology, 2020 Jul;18(7):e3000410
Cited work 2:
The ARRIVE reporting checklist, The EQUATOR Network reporting guideline platform, The UK EQUATOR Centre, 2025
Authors cited:
Sert NP; Hurst V; Ahluwalia A; Alam S; Avey MT; Baker M; et al.
Intended users:
Authors preparing manuscripts on animal research
Purpose:
To document adherence to reporting standards in animal experiments
Year:
2021
Region / city:
Not specified
Topic:
eDRX cycles
Document Type:
Draft
Organization / Institution:
3GPP TSG-RAN WG2
Author:
vivo, Qualcomm, OPPO, Huawei, HiSilicon, Xiaomi, Samsung, LGE
Target audience:
Members of the 3GPP working groups
Period of validity:
August 2021
Approval Date:
Not specified
Date of changes:
Not specified
Year:
2020
Region / City:
e-Meeting, May 25th – June 5th
Theme:
Enhanced Configured Grant Transmission for URLLC
Document Type:
Email Discussion
Organization / Institution:
3GPP TSG RAN WG1
Author:
Chairman
Target Audience:
Members of 3GPP TSG RAN WG1
Period of Validity:
Until May 29th, 2020
Date of Approval:
May 25th, 2020
Date of Changes:
Not specified
Year:
2026
Region / City:
Seoul, Korea
Topic:
Medical Research, Genome Editing, Ophthalmology
Document Type:
Research Article
Organization / Institution:
Seoul National University Hospital, Seoul National University College of Medicine
Author:
Jeong Hun Kim
Target Audience:
Researchers, Clinicians, Medical Professionals
Period of Effect:
Ongoing
Approval Date:
Not specified
Date of Changes:
Not specified
Contextual Description:
Research article presenting recent experimental results and clinical trial preparations regarding in vivo genome editing for treating vision-threatening retinopathies, such as AMD, DR, and ROP.
In Vivo Anti-Inflammatory and Anti-Nociceptive Activities of Aerial Part Extracts of Zehneria scabra
Year:
Not specified
Journal:
International Journal of Pharmacy and Industrial Research
ISSN (Print):
2231–3648
ISSN (Online):
2231–3656
Article Type:
Research Article
Author:
Baye Akele
Affiliation:
University of Gondar, College of Medicine and Health
Address:
P.O Box 196, Gondar, Ethiopia
Email:
[email protected]
Study Subject:
Zehneria scabra (Cucurbitaceous family)
Study Design:
In vivo experimental study
Experimental Models:
Acetic acid–induced writhing test; Carrageenan-induced inflammation
Extraction Method:
80% methanol extraction by maceration
Test Organisms:
Swiss albino mice (18–25 g)
Region of Plant Collection:
North east Ethiopia
Plant Identification Repository:
National Herbarium, Botanic Laboratory, Addis Ababa University, Ethiopia
Keywords:
Antinociceptive, Anti-inflammatory, Zehneria scabra, Maceration
Year:
2023
Region / city:
N/A
Subject:
Immunology, Cell Biology
Document type:
Supplementary Table
Organization:
N/A
Author:
N/A
Target audience:
Researchers, scientists in immunology and cell biology
Period of validity:
N/A
Approval date:
N/A
Date of changes:
N/A
Exempt Distribution of Carbon14 Urea Capsules for In Vivo Diagnostic Use in Humans, Effective 1/2/98
Year:
1998
Agency:
U.S. Nuclear Regulatory Commission
Document Type:
Federal Regulation / Rule
Subject:
Radioactive Drugs, Licensing Exemptions
RATS ID:
19977
Effective Date:
1/2/1998
CFR Sections:
30.21, 32.21, 32.21a
Usage Restrictions:
In vivo diagnostic use for humans only; not for research involving human subjects; not for incorporation into food, beverages, cosmetics, or other drugs
License Requirements:
Specific license required for commercial distribution, manufacture, or research use
Labeling Requirements:
Must indicate radioisotope, physical/chemical form, activity, and usage restrictions
Year:
2016
Institution:
University of Wisconsin–Madison
Document type:
Request for Bid / Contract Solicitation
Contract number:
17-5725-R1
Issue date:
8/17/16
Due date:
8/31/16, 2:00 PM CDT
Agent:
Janet Bresnahan
Scope:
In Vivo Drug Discovery Pharmacology Assays, Pharmacokinetics and Dose Tolerability in Rodents
Contract duration:
One year from award, automatically renewable for two additional one-year terms
Bid submission requirements:
Hard copy, CD/DVD/Flash drive, signatures required
Applicable rules:
Federal procurement rules, University standard terms and conditions
Sections included:
Submittal Instructions, General Information, RFB Process Instructions, Bidder Qualifications, Performance and Contract Requirements, Attachments A–H
Audience:
Potential vendors and contractors for pharmacology research services
Contextual description:
Official bid solicitation detailing requirements, procedures, and conditions for vendors to provide in vivo pharmacology testing services at the University of Wisconsin–Madison under a specified contract.
Year:
2016
Region / City:
Shanghai, China; Shenzhen, China; Suzhou, China; Helsinki, Finland; Turku, Finland
Subject:
Tissue engineering, vascularization, skin flap regeneration
Document Type:
Peer-reviewed research article
Institution / Organization:
Shanghai Ninth People’s Hospital, Xi’an Jiaotong University, Shenzhen Institutes of Advanced Technology, University of Helsinki, Soochow University, Åbo Akademi University
Authors:
Xiaoming Sun, Qi Lang, Hongbo Zhang, Liying Cheng, Ying Zhang, Guoqing Pan, Xin Zhao, Huilin Yang, Yuguang Zhang, Hélder A. Santos, Wenguo Cui
Target Audience:
Researchers in biomedical engineering and regenerative medicine
Methodology:
Electrospinning of photocrosslinkable gelatin methacryloyl (GelMA) hydrogels
Key Findings:
Enhanced endothelial cell adhesion, proliferation, migration, tubulogenesis, and increased skin flap survival in rat models
Publication DOI:
10.1002/adfm.201604617
Access:
Non-commercial use under Wiley Terms and Conditions
Year:
2023
Region / City:
Not specified
Topic:
Fetal cardiac function, hypoxic pregnancy, echocardiography
Document type:
Scientific research article
Institution:
Not specified
Authors:
Patey, KL Botting, Y Niu, L Zhang, J Ma, SG Ford, W Tong, CM Coutinho, B Thilaganathan, DA Giussani
Target audience:
Researchers, clinicians, scientists in the field of prenatal health, cardiology, and animal models
Period of validity:
Not specified
Approval date:
Not specified
Date of revisions:
Not specified