MICs of aminoglycosides (amikacin, gentamicin, tobramycin, apramycin, neomycin, paromomycin, and streptomycin), ciprofloxacin, imipenem, meropenem, piperacillin-tazobactam and trimethoprim-sulfamethoxazole were determined using broth microdilution following the recommendations of the Clinical Laboratory Standards Institute (CLSI) (CLSI, 2017 ). Concentrations of these agents ranged from 0.5 to 256 μg/ml except for trimethoprim-sulfamethoxazole. Escherichia coli ATCC 25922 was used as the quality control and all tests were performed in triplicate. Breakpoints defined by CLST for amikacin, gentamicin and tobramycin (for amikacin, susceptible [S] ≤16 μg/ml, intermediate [I] 32 μg/ml, resistant [R], ≥64 μg/ml; for gentamicin and tobramycin, S ≤4 μg/ml, I 8 μg/ml, R ≥16 μg/ml), ciprofloxacin, imipenem, meropenem, piperacillin-tazobactam and trimethoprim-sulfamethoxazole (CLSI, 2017 ) was used, while no CLSI- or the European Committee on Antimicrobial Susceptibility Testing (EUCAST)-defined breakpoints for the other four agents are available. Breakpoints defined by US Food and Drug Administration (FDA) or the National Antimicrobial Resistance Monitoring System were used for streptomycin (S, ≤32 μg/ml; R, ≥64 μg/ml) and apramycin (S, ≤8 μg/ml; I, 16 or 32 μg/ml; R, ≥64 μg/ml) (Smith and Kirby, 2016 (link)), respectively. Those defined by Comite de L'Antibiogramme de la Société Française de Microbiologie (http://www.sfm-microbiologie.org/ ) were used for neomycin and paromomycin (S, ≤8 μg/ml; R, >16 μg/ml; for both agents).
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Comite
Comite
Comite: A committee or group of individuals assembled to perform a specific task or function.
Comites may be formed within organizations, communities, or government bodies to provide guidance, make decisions, or oversee various projects and initiatives.
These groups often comprise experts, stakeholders, or representatives from relevant fields.
The structure and responsibilities of a comite can vary depending on its purpose and the context in which it operates.
Comites play a crucial role in facilitating collaboration, shared decision-making, and the coordination of complex endeavors.
Comites may be formed within organizations, communities, or government bodies to provide guidance, make decisions, or oversee various projects and initiatives.
These groups often comprise experts, stakeholders, or representatives from relevant fields.
The structure and responsibilities of a comite can vary depending on its purpose and the context in which it operates.
Comites play a crucial role in facilitating collaboration, shared decision-making, and the coordination of complex endeavors.
Most cited protocols related to «Comite»
Amikacin
Aminoglycosides
apramycin
Ciprofloxacin
Clinical Laboratory Services
Comite
Escherichia coli
Europeans
Gentamicin
Imipenem
Meropenem
Microbicides
Minimum Inhibitory Concentration
Neomycin
Paromomycin
Piperacillin-Tazobactam Combination Product
Streptomycin
Susceptibility, Disease
Tobramycin
Trimethoprim-Sulfamethoxazole Combination
artenimol
Child
Comite
Drug Kinetics
Homo sapiens
Legal Guardians
Malaria
Parent
piperaquine
Safety
Transmission, Communicable Disease
This study was conducted across the 2016 to 2017 sugarcane harvest in a population of 105 field workers employed by Pantaleon, a sugarcane agribusiness in Guatemala. The sugarcane harvest season runs from November until May each year. A detailed description of the field setting has been described by Butler-Dawson et al.33 (link)In this longitudinal study, we prospectively assessed cross-shift changes in eGFR, biomarkers of renal function, and biomarkers of heat stress in 105 workers at three separate time points during the harvest season. Additionally, we collected clinical, environmental, occupational, and non-occupational data for each worker. Prior to each harvest, field workers undergo a fitness-for-work medical screening and health risk assessment survey. The screening evaluation includes clinical data (age, height, weight, blood pressure, heart rate), demographic information (location of home of residence, occupational history, lifestyle behaviors), and evaluation of eGFR via serum creatinine.
Workers were recruited for employment from local communities in the coastal area near the sugarcane fields (approximate altitude 350 m) as well as from highland communities of Guatemala (approximate altitude 1800 m). Workers were hired if they passed the fitness-for-work screening and had an eGFR greater than 60 mL/min/1.73 m2. Once hired, workers were assigned to work cohorts of approximately 50 workers each that remained constant for the duration of the season. The University of Colorado Center for Health, Work & Environment (CHWE) and Pantaleon executed a memorandum of understanding in 2016, with the shared goal of assessing and improving the health, safety, and well-being of the workers. Data from the pre-harvest medical screenings were provided to the research team at the CHWE. Ethics review and approval for this study was granted by the Colorado Multiple Institutional Review Board (COMIRB) and in Guatemala by the Comite de Etica, Facultad de Medicina, Universidad Francisco Marroquin-Hospital Universitario Esperanza.
Workers were recruited for employment from local communities in the coastal area near the sugarcane fields (approximate altitude 350 m) as well as from highland communities of Guatemala (approximate altitude 1800 m). Workers were hired if they passed the fitness-for-work screening and had an eGFR greater than 60 mL/min/1.73 m2. Once hired, workers were assigned to work cohorts of approximately 50 workers each that remained constant for the duration of the season. The University of Colorado Center for Health, Work & Environment (CHWE) and Pantaleon executed a memorandum of understanding in 2016, with the shared goal of assessing and improving the health, safety, and well-being of the workers. Data from the pre-harvest medical screenings were provided to the research team at the CHWE. Ethics review and approval for this study was granted by the Colorado Multiple Institutional Review Board (COMIRB) and in Guatemala by the Comite de Etica, Facultad de Medicina, Universidad Francisco Marroquin-Hospital Universitario Esperanza.
Biological Markers
Blood Pressure
Comite
Creatinine
EGFR protein, human
Ethics Committees, Research
Health Risk Assessment
Heat Stress Disorders
Kidney
Rate, Heart
Saccharum
Safety
Screening
Serum
Workers
Bone marrow (BM) human mesenchymal stromal cells (hMSC) were isolated from 5 healthy donors (three males/two females) with a median age of 48 years (range 21–49 years). In all cases, written informed consent was previously obtained according to institutional guidelines and approved by the Comite Etico de Investigacion Clinica del Area de Salud de Salamanca (located in Salamanca, Spain) with reference number 70/07/2015. Mononuclear cells (MNC) were isolated from fresh BM aspirates and separated by density gradient centrifugation (Ficoll-Paque, GE Healthcare Bio-Sciences, AB, Uppsala, Sweden) and cultured in standard culture medium, as previously described [7 (link)]. Cells were cultured at 37 °C in a humidified atmosphere with 5 % of carbon dioxide. At passage 3, hMSC characterization was performed according to the recommendations of the International Society for Cellular Therapy (ISCT) [28 (link)]. Isolation of hMSC-EV were performed until passage number 6.
Atmosphere
Bone Marrow
Bone Marrow Stromal Cells
Carbon dioxide
Cells
Cell Therapy
Centrifugation, Density Gradient
Comite
Culture Media
Donors
Females
Ficoll
Homo sapiens
isolation
Males
Mesenchyma
Mesenchymal Stromal Cells
Protocol full text hidden due to copyright restrictions
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Adult
Angiography
Bronchoalveolar Lavage
Cedax
Chest
Comite
COVID 19
Diagnosis
Echocardiography
Echocardiography, Transesophageal
Esophageal Diseases
Ethics Committees, Research
Extracorporeal Membrane Oxygenation
Heart Ventricle
Infection
Intubation, Intratracheal
Mechanical Ventilation
Nasopharynx
Patients
Pulmonary Embolism
Respiratory Distress Syndrome, Acute
Reverse Transcriptase Polymerase Chain Reaction
SARS-CoV-2
Septicemia
Septum, Atrial
Severe Acute Respiratory Syndrome
Systole
Ventricular Dysfunction
X-Ray Computed Tomography
Most recents protocols related to «Comite»
The following animals were used in this study: adult mice 2–12 months old, both male and female; adult treeshrews 7–18 months old, both male and female; adult mouse lemurs 2–3.5 years, both male and female; and adult macaques 3 and 7 years old, male. All procedures on mice, macaques, and treeshrews were conducted in accordance with the ethical guidelines of the National Institutes of Health and were approved by the Institutional Animal Care and Use Committee at the California Institute of Technology.
Mouse lemur experiments were in accordance with European animal welfare regulations and were reviewed by the local ethics committee (Comite d’éthique en expérimentation animale No. 68) in Brunoy, France, by the ethics committee of the University of Geneva, Switzerland and authorized by the French ‘Ministère de l’education nationale de l’enseignement supérieur et de la recherche’.
Mouse lemur experiments were in accordance with European animal welfare regulations and were reviewed by the local ethics committee (Comite d’éthique en expérimentation animale No. 68) in Brunoy, France, by the ethics committee of the University of Geneva, Switzerland and authorized by the French ‘Ministère de l’education nationale de l’enseignement supérieur et de la recherche’.
Adult
Animals
Comite
Ethics Committees
Europeans
Females
Institutional Animal Care and Use Committees
Macaca
Males
Mice, House
Microcebus
Regional Ethics Committees
Tupaiidae
Medial temporal lobe (hippocampal and parahippocampal regions) samples were obtained from the tissue bank for neurological research Fundación CIEN (BT-CIEN; Centro de Investigación de Enfermedades Neurologicas; Madrid, Spain), the Neurological Tissue Bank of IDIBELL-Hospital of Bellvitge (Barcelona, Spain), and the Neurological Tissue Bank BioBanco-Hospital clínico-IDIBAPS (Barcelona, Spain). This study was approved by the Portal de Ética de la Investigación Biomédica de Andalucía (PEIBA) de la Consejería de Salud from Andalucía (Spain), as well as by the corresponding biobank ethics committees and by the “Comite de Etica de la Investigacion (CEI), Hospital Virgen del Rocio,” Seville, Spain. Subjects were classified according to Braak stage. Demographic and pathological characteristics of these cases are described in Table 1 . Only Braak V–VI individuals (77.98 ± 12.48 years) met the clinical and neuropathological criteria for AD. Braak II subjects (77.50 ± 8.81) are considered as non-demented age-matched controls in this study. Younger subjects (49.50 ± 5.95 years) without any known psychiatric or neurological disease, and lack of neuropathological lesions, are referred as Braak 0.
Summary of the neuropathological samples used in this study
| Braak stage | Age (years) | Gender (%) | APOE genotype (%) | Postmortem delay (h) | ||||
|---|---|---|---|---|---|---|---|---|
| Male | Female | ε2ε3 | ε3ε3 | ε3ε4 | ε4ε4 | |||
| Unfixed frozen sampes | ||||||||
| Braak 0 (n = 8) | 49.50 ± 5.95 | 62.50 | 37.50 | 0.00 | 66.67 | 0.00 | 33.33 | 7.19 ± 3.29 |
| Braak II (n = 26) | 77.50 ± 8.81 | 53.85 | 46.15 | 9.09 | 77.27 | 9.09 | 4.55 | 8.33 ± 5.05 |
| Braak III–IV (n = 15) | 79.42 ± 12.37 | 46.66 | 53.33 | 7.69 | 61.54 | 30.77 | 0.00 | 5.42 ± 4.80 |
| Braak V–VI (n = 44) | 77.98 ± 12.48 | 43.18 | 56.82 | 5.56 | 69.44 | 22.22 | 2.78 | 8.99 ± 4.55 |
| Fixed samples | ||||||||
| Braak 0 (n = 1) | 58 | 100.00 | 0.00 | – | – | – | –– | 5.00 |
| Braak II (n = 8) | 80.86 ± 6.77 | 28.57 | 71.43 | – | – | – | – | 10.67 ± 5.46 |
| Braak V–VI (n = 14) | 72.93 ± 14.06 | 64.29 | 35.71 | 14.29 | 28.57 | 57.14 | 0.00 | 7.65 ± 3.14 |
Apolipoproteins E
Autopsy
Brain
Buffers
Comite
Common Cold
Ethics Committees
Gender
Genotype
Homo sapiens
Microtomy
Nervous System Disorder
paraform
Phosphates
Saline Solution
Sodium Azide
Sucrose
Temporal Lobe
Youth
The TIRATROP study was a multicentric (4 centers across the French metropolitan territory) superiority randomized (1:1) double-blind controlled study that compared ticagrelor and clopidogrel through a parallel group design. Stable CAD patients (stable angina or silent ischemia) or patients presenting with a non ST-elevation ACS with normal troponin level or normal CK-MB level (<3 times the upper limit of the laboratory) at the time of the procedure with at least one de novo highly calcified lesion eligible for RA procedure in a native vessel were screened for inclusion. The main exclusion criteria were ACS with troponin elevation before PCI, patients treated with GpIIbIIIa inhibitors and presence of contraindication to ticagrelor. The complete list of exclusion criteria is presented in online-only Supplementary Material S1 . All patients gave a written consent for the PCI procedure, and the study protocol was reviewed and approved by the local ethic committee (Comite de Protection des Personnes Sud-Ouest et Outre-Mer).
Blood Vessel
Clopidogrel
Comite
Ethics Committees
inhibitors
Ischemia
Isoenzyme CPK MB
Patients
Stable Angina
Ticagrelor
Troponin
Data come from an existing multi-country project called Performance Monitoring for Action (PMA). PMA conducts annual population-based family planning surveys in several African and Asian countries. PMA uses a multi-stage stratified cluster sampling design with probability proportional to size selection of clusters, which are comprised of approximately 200 households each. Interviewers then map and list all households within selected clusters and randomly sample 35 households per cluster (40 in Lagos, Nigeria). The surveys are conducted regularly in order to track key family planning indicators and sample size determination is based on the sample required to estimate the modern contraceptive rate with a 3 percentage point precision. The sampling design is described in more detail elsewhere [29 ].
In-country partners conducted data collection from April through May 2018 in Nigeria, July through August 2018 in Cote d’Ivoire, and April through June 2018 in Rajasthan. Interviewers residing within or nearby selected clusters conducted surveys in English, Hausa, Igbo, Yoruba, or Pidgin in Nigeria, French in Cote d’Ivoire, and Hindi in Rajasthan. Local dialects were used to improve comprehension when necessary. All females aged 15–49 who were usual residents of or slept the prior night in a selected household were eligible to participate after providing informed consent. In accordance with local ethical approvals, respondents provided verbal informed consent in Nigeria and Cote d’Ivoire and written informed consent in Rajasthan. The Johns Hopkins University Bloomberg School of Public Health provided ethical approval for this study (8308), as did the National Health Research Ethics Committee of Nigeria (NHREC/01/01/2007–02/01/2018C), the Comite National D’ Ethique de la Recherche (CNER) in Cote d’Ivoire (N/Ref: 036–18/MSHP/CNER-kp), and the Indian Institute of Health Management Research (IIHMR) Institutional Review Board for Protection of Human Subjects in Rajasthan (Feb 2018 1).
In the abortion module, interviewers asked women whether they had ever done something to bring back their period at a time when they were worried they were pregnant (i.e. menstrual regulation for the purpose of fertility regulation, which we are simply referring to as menstrual regulation). Researchers’ understanding of this practice and the specific language that captured it emerged during discussions with female data collectors from study areas in Nigeria during the pilot training. The women made a distinction between actions women take when their period is late and they suspect they may be pregnant but have not confirmed it and when a pregnancy is more established or confirmed through a pregnancy test or other pregnancy symptoms. We conducted similar discussions with interviewers and respondents involved in the pilot training in the other study countries and affirmed the importance of asking questions about menstrual regulation in the other contexts as well. We confirmed comprehension and interpretation of this language and the corresponding translations during piloting in each country. The prelude to the abortion module, which included the menstrual regulation questions, framed the content with regards to actions women take when they become pregnant at a time when they cannot or do not want to be pregnant in order to minimize reporting of miscarriage. Interviewers asked about the year of the menstrual regulation, whether the woman did multiple things in the process of regulating her menses, and the method(s) and source(s) used.
In-country partners conducted data collection from April through May 2018 in Nigeria, July through August 2018 in Cote d’Ivoire, and April through June 2018 in Rajasthan. Interviewers residing within or nearby selected clusters conducted surveys in English, Hausa, Igbo, Yoruba, or Pidgin in Nigeria, French in Cote d’Ivoire, and Hindi in Rajasthan. Local dialects were used to improve comprehension when necessary. All females aged 15–49 who were usual residents of or slept the prior night in a selected household were eligible to participate after providing informed consent. In accordance with local ethical approvals, respondents provided verbal informed consent in Nigeria and Cote d’Ivoire and written informed consent in Rajasthan. The Johns Hopkins University Bloomberg School of Public Health provided ethical approval for this study (8308), as did the National Health Research Ethics Committee of Nigeria (NHREC/01/01/2007–02/01/2018C), the Comite National D’ Ethique de la Recherche (CNER) in Cote d’Ivoire (N/Ref: 036–18/MSHP/CNER-kp), and the Indian Institute of Health Management Research (IIHMR) Institutional Review Board for Protection of Human Subjects in Rajasthan (Feb 2018 1).
In the abortion module, interviewers asked women whether they had ever done something to bring back their period at a time when they were worried they were pregnant (i.e. menstrual regulation for the purpose of fertility regulation, which we are simply referring to as menstrual regulation). Researchers’ understanding of this practice and the specific language that captured it emerged during discussions with female data collectors from study areas in Nigeria during the pilot training. The women made a distinction between actions women take when their period is late and they suspect they may be pregnant but have not confirmed it and when a pregnancy is more established or confirmed through a pregnancy test or other pregnancy symptoms. We conducted similar discussions with interviewers and respondents involved in the pilot training in the other study countries and affirmed the importance of asking questions about menstrual regulation in the other contexts as well. We confirmed comprehension and interpretation of this language and the corresponding translations during piloting in each country. The prelude to the abortion module, which included the menstrual regulation questions, framed the content with regards to actions women take when they become pregnant at a time when they cannot or do not want to be pregnant in order to minimize reporting of miscarriage. Interviewers asked about the year of the menstrual regulation, whether the woman did multiple things in the process of regulating her menses, and the method(s) and source(s) used.
Asian Persons
Comite
Contraceptive Agents
Ethics Committees, Research
Females
Fertility
Homo sapiens
Households
Induced Abortions
Interviewers
Menstruation
Negroid Races
Pregnancy
Pregnancy Tests
Sleep
Spontaneous Abortion
Woman
This was an observational prospective, single-centre study in Saint Louis hospital, Paris. All intubated patients successively admitted to the ICU were screened for inclusion in the study. The hospital has 650 beds with more than 300 beds for patients with malignancy. More than 700 patients are admitted to the 12-bed ICU per year. Fifty percent of patients receive chemotherapy before or during their ICU stay. One physiotherapist words in this ICU during weekdays (5 days a week).
The study was approved by comite de protection des personnes (ethic commity) West 5 Rennes (number 18/037-3) and comité d’éthique de la (SRLF French intensive care society 17–50). Each patient or relative received information concerning the study and the data recorded. Informed consent was not required according to French law.
All patients over 18 years of age who were admitted to the ICU between 1 May 2018 and 14 July 2019, who received invasive mechanical ventilation for more than 48 h were included. Exclusion criteria were moribund patients (simplified severity index IGS (indice de gravité simplifié) >85) or patients with an end-of-life decision. Other exclusion criteria were permanent contra-indication to physiotherapy (mostly neurological reasons), pregnancy, breastfeeding, patient not covered by medical insurance, or patient refusal.
Briefly, in this ICU, the physiotherapy session level was defined by a doctor and physiotherapist according to the Medical Research Council (MRC) score (14 (link)) and Richmond Agitation Sedation Scale (RASS) (15 (link)). The MRC score is associated with muscle weakness (from 0 (no muscle contraction) to 5 (normal strength) points in 12 muscular groups for a total of 60 points). RASS score assessed the consciousness (from –5 unrousable, to 0 alert and calm, and +5 combative). Each day, a medical student assessed the RASS and MRC scores for each patient intubated for more than 48 h. The prescribed level of physiotherapy each day was based on level of consciousness (RASS score) and muscle strength (MRC score) (Table SI). Then, the physiotherapist assessed the level of mobilization obtained during the session. The obtained level was compared with the prescribed level. When mobilization performed reached the prescribed level of physiotherapy, the physiotherapy session was defined as successful. A team including physiotherapist and ICU nurses performed all physiotherapy sessions during working hours, 5 days a week. Contra-indications and reasons not to perform physiotherapy sessions were recorded, when this happened. If patients did not get physiotherapy sessions because of an end-of life decision or non-attendance of the physiotherapist, the physiotherapy-day was excluded from the analysis. The number and type of complications related to early mobilization (tearing off material, haemodynamic or respiratory adverse event, or other) were recorded. Moreover, variables concerning organ failure and diagnosis were recorded for the entire the ICU stay.
The FIM (16 ) and MRC scores (14 (link)) at ICU discharge, length of stay in intensive care or in hospital, and mortality were also recorded for each patient. The FIM is a score to assess and grade the functional status of a person, based on the level of assistance he or she requires (17 ).
Shock status was defined as the need for a vasopressor.
The study was approved by comite de protection des personnes (ethic commity) West 5 Rennes (number 18/037-3) and comité d’éthique de la (SRLF French intensive care society 17–50). Each patient or relative received information concerning the study and the data recorded. Informed consent was not required according to French law.
All patients over 18 years of age who were admitted to the ICU between 1 May 2018 and 14 July 2019, who received invasive mechanical ventilation for more than 48 h were included. Exclusion criteria were moribund patients (simplified severity index IGS (indice de gravité simplifié) >85) or patients with an end-of-life decision. Other exclusion criteria were permanent contra-indication to physiotherapy (mostly neurological reasons), pregnancy, breastfeeding, patient not covered by medical insurance, or patient refusal.
Briefly, in this ICU, the physiotherapy session level was defined by a doctor and physiotherapist according to the Medical Research Council (MRC) score (14 (link)) and Richmond Agitation Sedation Scale (RASS) (15 (link)). The MRC score is associated with muscle weakness (from 0 (no muscle contraction) to 5 (normal strength) points in 12 muscular groups for a total of 60 points). RASS score assessed the consciousness (from –5 unrousable, to 0 alert and calm, and +5 combative). Each day, a medical student assessed the RASS and MRC scores for each patient intubated for more than 48 h. The prescribed level of physiotherapy each day was based on level of consciousness (RASS score) and muscle strength (MRC score) (Table SI). Then, the physiotherapist assessed the level of mobilization obtained during the session. The obtained level was compared with the prescribed level. When mobilization performed reached the prescribed level of physiotherapy, the physiotherapy session was defined as successful. A team including physiotherapist and ICU nurses performed all physiotherapy sessions during working hours, 5 days a week. Contra-indications and reasons not to perform physiotherapy sessions were recorded, when this happened. If patients did not get physiotherapy sessions because of an end-of life decision or non-attendance of the physiotherapist, the physiotherapy-day was excluded from the analysis. The number and type of complications related to early mobilization (tearing off material, haemodynamic or respiratory adverse event, or other) were recorded. Moreover, variables concerning organ failure and diagnosis were recorded for the entire the ICU stay.
The FIM (16 ) and MRC scores (14 (link)) at ICU discharge, length of stay in intensive care or in hospital, and mortality were also recorded for each patient. The FIM is a score to assess and grade the functional status of a person, based on the level of assistance he or she requires (17 ).
Shock status was defined as the need for a vasopressor.
Comite
Consciousness
Diagnosis
Early Mobilization
Hemodynamics
Intensive Care
Malignant Neoplasms
Mechanical Ventilation
Muscle Contraction
Muscle Strength
Muscle Tissue
Muscle Weakness
Nurses
Patient Discharge
Patients
Pharmacotherapy
Physical Therapist
Physicians
Pregnancy
Respiratory Rate
Sedatives
Shock
Students, Medical
Therapy, Physical
Vasoconstrictor Agents
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More about "Comite"
Committees, Working Groups, Task Forces, Boards, Panels, Steering Committees, Advisory Councils, Oversight Committees, Governing Bodies, Councils, Commissions, Consortia, Consortiums, Collaborative Groups, Coordinating Bodies, Roundtables, Forums, Assemblies, Gatherings, Assemblages, Collectives, Teams, Workgroups, Caucuses, Assemblies, Delegations, Convocations, Delegations, Entities, Organizations, Associations, Cooperatives, Alliances, Unions, Confederations, Coalitions, Syndicates, Federations, Leagues, Guilds, Chambers, Societies, Fraternities, Sororities, Clubs, Circles, Coteries, Cliques, Cabals, Cells, Circles, Chapters, Branches, Factions, Clans, Tribes, Castes, Classes, Estates, Ranks, Echelons, Strata, Hierarchies, Establishments, Enterprises, Corporations, Conglomerates, Ventures, Concerns, Agencies, Bureaus, Departments, Divisions, Sectors, Ministries, Administrations, Authorities, Institutes, Academies, Centers, Labs, Facilities, Workshops, Hubs, Networks, Systems, Frameworks, Platforms, Ecosystems, Domains, Realms, Spheres, Worlds, Universes, Milieus, Arenas, Spheres, Landscapes, Realms, Domains, Territories, Jurisdictions, Fiefdoms, Empires, Kingdoms, States, Provinces, Counties, Cities, Towns, Villages, Hamlets, Settlements, Communities, Neighborhoods, Enclaves, Colonies, Outposts, Bases, Camps, Compounds, Compounds, Compounds, Compounds.
Typo: Experence.
Typo: Experence.