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Barstow College  留言于2019-03-27 01:40:11 |
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评论：UPDATE - From The Chinese American Professors and Professionals Network (2019 No.7) |
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Hello,
Please review the link below and forward to anyone interested in applying. The current job vacancies with Barstow College are:
CLASSIFIED:
Database Analyst
CERTIFICATED:
Athletic Director/Faculty (70/30)
Mental Health Counselor – Grant Funded
MANAGEMENT:
Dean of Instruction
Director, Public Relations, Communications and Marketing
Vice President, Academic Affairs
Vice President, Administrative Services
Vice President, Student Services
Visit https://www.schooljobs.com/careers/barstowcc to apply.
Sincerely,
Human Resources Office
Barstow College
rpalakiko@barstow.edu
760-252-2411 EXT. 7231 |
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内蒙古大学人事处 留言于2019-03-26 10:14:50 |
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评论：UPDATE - From The Chinese American Professors and Professionals Network (2019 No.6) |
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美国华裔教授专家网
您好，我们是内蒙古大学人事处，我校为实现人才战略大布局，并按学校事业发展需要，决定面向全球招聘高层次人才。特有请贵处协助我校将“2019年面向海内外招聘高层次人才公告”发布在贵处网站相关栏目。非常希望能得到您们的帮助。给您工作上带来的打扰表示歉意并感谢您帮助刊登！
招聘公告链接：http://www.imu.edu.cn/info/1032/1340.htm
内蒙古大学（Inner Mongolia University），是国务院1978年确定的88所全国重点大学之一，是英国《简明大不列颠百科全书》所列中国15所著名大学之一，首批国家“211工程”重点建设的高校。创建于1957年，是新中国成立后在少数民族地区最早创立的一所综合性大学，在国家高等教育布局中具有重要作用和特殊区域定位。2004年成为内蒙古自治区和教育部重点共建大学，2012年入选首批国家“中西部高校综合实力提升工程”高校。有28个省部级重点实验室、工程技术研究中心、人文社会科学重点研究基地。
期待您的回复
内蒙古大学人事处
电话：0471-4992415
ndszk@imu.edu.cn |
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U.S. Food & Drug Administration 留言于2019-03-26 09:55:17 |
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评论：UPDATE - From The Chinese American Professors and Professionals Network (2019 No.6) |
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The FDA has recently approved the following devices to be marketed （Part 2）
VENTANA PD-L1 (SP142) Assay - P160002/S009
This is a test done in a laboratory using samples from triple negative breast cancer patients which doctors use to see if patients have programmed cell death ligand (PD-L1) in their cancer.
MitraClip NT Clip Delivery System and MitraClip NTR/XTR Clip Delivery System - P100009/S028
The MitraClip NT Clip Delivery System and MitraClip NTR/XTR Clip Delivery System are two newer models of the MitraClip Clip Delivery System approved previously by the FDA. Each system contains a permanent implant that looks and functions like a clip. The clip is used to grasp the two leaflets of the mitral valve in the heart and clip them together to reduce the backflow of blood (called mitral regurgitation or MR). The current application expands the system’s indications for use to include secondary (or functional) MR, when MR is caused by a dysfunctional left ventricle, not by degeneration of the mitral valve itself.
VENOVO Venous Stent System - P180037
The VENOVO Venous Stent System is intended to treat a narrowed vein found in the upper pelvic region down to the groin area (iliofemoral vein). The VENOVO Venous Stent System has two components: a stent made of a nickel-titanium alloy (nitinol) tubing and an over-the-wire stent delivery catheter system.
OPTIMIZER Smart System - P180036
The OPTIMIZER Smart System includes an implantable pulse generator (IPG), a charging system and a programmer. The IPG monitors the heart’s activity and delivers non-excitatory electrical signals (cardiac contractility modulation therapy) to the right ventricle of the heart in patients with chronic heart failure. The charging system is used to recharge the IPG and the programmer to allows medical personnel to control the settings of the device.
COVERA™ Vascular Covered Stent - P170042/S002
The Covera™ Vascular Covered Stent is an expandable, flexible, metal (nitinol) tube-shaped device (stent) that is covered with a material called expanded polytetrafluoroethylene (ePTFE). Each covered stent is mounted on the end of a delivery catheter system. The device was previously approved for use in the treatment of stenoses at the venous anastomosis of ePTFE or other synthetic arterio-venous (AV) access grafts only. In this PMA supplement, FDA approved this device for the treatment of a narrowing (stenosis) or blockage which has developed anywhere in the access circuit of patients on hemodialysis using an Arteriovenous (AV) Fistula. |
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U.S. Food & Drug Administration 留言于2019-03-26 09:50:18 |
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评论：UPDATE - From The Chinese American Professors and Professionals Network (2019 No.6) |
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The FDA has recently approved the following devices to be marketed （Part1）：
Resolute Integrity Zotarolimus Eluting Coronary Stent System - P110013/S088
The Resolute Integrity Zotarolimus Eluting Coronary Stent System is a drug-coated device that contains two components: the stent and the catheter delivery system with a balloon that will inflate to deploy the stent. The stent is placed into a blood vessel (coronary artery) supplying blood to the heart and helps to keep the coronary artery open. The current approval expands the indications for use to include treatment of a blocked coronary artery (chronic total occlusion).
Sangia Total PSA Test - P170037
The Sangia Total Prostate Specific Antigen (PSA) Test consists of a Cassette Assembly and a Sample Collector. The Sangia Total PSA Test is used as an aid in the diagnosis of prostate cancer. This new test is the first point-of-care test that can deliver PSA results near where the patient is being evaluated, for example at the doctor's office, instead of waiting for lab analysis. The test can be administered with a simple finger prick, and results are generated in less than 15 minutes. Prostate-specific antigen, or PSA, is a protein produced by cancerous, as well as noncancerous tissue in the the prostate gland. The PSA test measures the level of PSA in a man's blood.
MANTA Vascular Closure Device - P180025
The MANTA Vascular Closure Device is a system designed to close large puncture sites in one of the large vessels in the leg (femoral artery) following catheterization procedures. The system is a polymer component (toggle) attached to a collagen plug and a delivery system used to place the toggle-collagen plug implant.
M6-C™ Artificial Cervical Disc - P170036
The M6-C™ Artificial Cervical Disc is an implant (device) that replaces the function of a damaged or diseased disc of the neck in the spine (C3-C7). The M6-C™ contains a series of polymer (ultra-high molecular weight polyethylene) fibers wound in a specific pattern. The fiber is wound around a polymer (polycarbonate urethane) core and through the slots in two titanium alloy inner endplates. The two titanium alloy inner endplates are welded to two titanium alloy outer endplates. The endplates attach to the patient's spinal bone and the implant is designed to maintain the natural movement of the spine.
Barricaid® Anular Closure Device (ACD) - P160050
The Barricaid® Anular Closure Device (ACD), also referred to as “Barricaid," is an implant (device) inserted in the spinal bone (vertebrae) of the lower back to try to prevent another herniated discs (reherniation). The Barricaid is made of titanium and is attached to a polyester (polyethylene terephthalate or commonly referred to as PET) flexible woven polymer fabric mesh. The Barricaid is intended to close the hole in a patient's spinal bone (vertebrae) following a limited discectomy procedure in the lower back (L4-S1) after an initial herniated disc. |
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editor@ijrdo.org 留言于2019-03-25 14:53:39 |
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评论：UPDATE - From The Chinese American Professors and Professionals Network (2019 No.6) |
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IJRDO Journal (https://ijrdo.org/)
editor@ijrdo.org
Call for Paper – March Issue 2019
International Journal for Research in Social Science and Humanities is an open access journal and provide 12 issues in a year. Green Publication is the publisher of this journal and provides many other journals in other fields of research like engineering and technology, medical and pharmaceutical, agricultural research etc. https://ijrdo.org/
Or Submit at the email – editor@ijrdo.org
Deadline of Submission – none
Publication time – at the end of every month
If you want to unsubscribe our journal. Please send a message on-jabbarkh769@gmail.com
Our Journals:-
To join our editorial board, or submit CV with current designation and institution at editor@ijrdo.org
Regards
IJRDO JOURNAL
editor@ijrdo.org
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jia00354 留言于2019-03-23 22:44:38 |
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评论：UPDATE - From The Chinese American Professors and Professionals Network (2019 No.6) |
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盐城巨爆案如果发生在朝鲜美方一定强烈谴责……可惜，这事儿发生在中国，美国就只能“谨言慎行”了。在悲痛中为盐城爆炸案叫好！用无辜人的生命消灭了一个人间“祸害致富集团”虽然有些悲哀凄凉，但就此除掉了盐城地区多年来污染环境大户，慢性放毒首恶，毁坏家园的恶魔，死也值得！这个罪恶累累的化工企业，多次因泄露毒气被罚、被判就是不被铲除、就是不倒。如果不是它自己爆炸连国务院都拿它没办法，可见后台之硬，保护伞之强大，贿赂手段之高超简直令人叹为观止。这次盐城爆炸事故与其说是人为的不如说是天意，在促犯众怒继续做恶的基础上又犯了天怒，因此是天意让它爆炸。人们在祈求人治无果的时候只有祈求天治，果不然上天有眼，它终于爆炸了。不过，不要高兴得太早，三个月后就息事宁人，四个月后就烟消云散，不出半年这个化工企业还得重新寻找地点再建，继续祸国殃民赚大钱。奇怪的是，这次巨爆后第一时间里央视就承认了是盐城巨爆，免得北韩跟着背了黑锅。 |
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WSL 留言于2019-03-23 22:37:13 |
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评论：UPDATE - From The Chinese American Professors and Professionals Network (2019 No.6) |
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前不久，蔡英文狗急跳墙，为了攻击国民党，把封存了多年的许多蒋介石原始手令、公文等曝光了出来，内容包括九一八之前张学良电询蒋介石日军即将发动攻击，然后蒋介石下令不抵抗的原始电报，蒋介石指示张学良放弃锦州来压孙科政府倒台的电报，”南京保卫战“始末、”苏区大烧杀……叹为观止。
不得不说，蔡同志这一手，不但狠狠打了国民党的脸，也狠狠打了许多”果粉“和”民国研究者“的脸。
一是南京保卫战，国军在长江边崩溃并不是唐生智的锅，而是蒋记中央军私扣船只丢下友军逃跑下关导致的。
二是蒋对于东北义勇军的态度就是让手下少管闲事让他们去死。
三是蒋介石的操作手令
四是蒋介石签署的对苏区的灭绝令，明令不要用轰炸，要用火油烧才杀的彻底。
五是张学良察觉到了日本要侵占东北，向蒋介石问计(求救)。
六是九一八后蒋介石下令在山东不抵抗，国民党大会蒋介石要求大家逆来顺受不要抵抗。
七是张学良给马占山下的中国对日战争第一个抵抗命令原件。
八是蒋介石命令张学良放弃锦州来压孙科政府倒台。
相关档案解密之后，国民党质疑蔡英文动机，却没有对档案真实性提出异议。大陆则是对此极为低调，那些曾经为蒋介石开脱的人也毫无反应。根据这些档案可以证明，张学良晚年为了顾及蒋介石的不杀之恩而自愿为蒋背黑锅。
九一八事变之后，蒋介石就连发电文，充分表达了对日方的“关怀”。
1931年9月20日，也就是九一八事变的第三天，蒋介石给地方长官发了一份电报，要求各地长官一定要保持克制，虽然日方侵略，但我们不能动，同时还要严格镇压老百姓的抗日运动，不能伤害友邦。
沈阳日军与我冲突，我政府正严重交涉中。各地方民众爱国心里之冲动，自所难免，但切不可有激烈反日运动及报复暴举。免人更有所藉口，使外交益陷困难。应力持镇静，严守秩序，请兄负责维持为要。
1931年10月7日，日军军舰开到镇江，蒋介石发电文命令地方警察局要照顾好日本海军，要关怀备至，还要帮他们买菜送到船上去。
日海军明日又来镇江，增加一艘。请注意，如其水兵上岸买菜等事，最好分与其交涉，由当地警局为其代买送船，以免纠纷。
1931年7月，蒋介石开始发动对苏区的三次“围剿”，在“围剿”行动中，蒋介石多次下令对苏区进行“大烧杀”。1931年8月16日，蒋介石在给赵观涛、卫立煌的手令中写道：
大小各村庄务全烧燬，勿遗。然后移动可也。凡我军所到之处，为匪化太深，不易防守者，皆可焚燬。
他命令国军所到之处，焚毁所有村庄，所谓“石要过刀，茅要过火，人要换种”，便是如此。8月21日的时候，蒋介石还不放心部下的手艺，开始指导“微操”，下手令给熊士辉，详细布置如何进行烧杀，细化到了如何放火，如何烧杀：
对匪巢只有焚烧，乃能解决，请派飞机设法暂停轰炸，而专用火油在欲烧之区域内，使皮带或分水壶分布火油。如此分划区域，每区约焚二三日，使匪恐慌，不能立足。
1933年8月30日，蒋介石给时任豫鄂皖边区剿匪军总司令刘镇华、鄂湘边区剿匪军总司令徐源泉下达手令，要求对鄂豫皖苏区进行“大烧杀”。蒋介石还在电文中卖弄学问，讲“剿”字的意义，要求国军对苏区民众斩草除根，杀戮殆尽。
潢川刘总司令、沙市徐总司令，密。匪化已深之区域非准各部队官兵尽量之烧杀，不能铲除匪根。即推“剿匪”之“剿”字，其意义亦必以刀入匪巢、杀戮尽净之意。否则不足尽剿匪之义，而乃养匪遗患而已。务令各部烧杀勿论为要。中正。 |
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