Join collection
Hello, welcome to our official website!
2018年终盘点:互联网保险创新和监管调试中稳步前行
2019-01-12

根据2018年10月份下发的《互联网保险业务监管办法(草稿)》(业界称为“《征求意见稿》”),互联网保险业务是指保险公司、保险中介机构依托互联网和移动通信等技术,通过自营网络平台、第三方网络平台等订立保险合同、提供保险服务的业务。截至2017年末,全国共有117家保险公司经营互联网保险,占保险公司总量的52.7%。

2018年互联网保险业务依然延续了近年来的迅猛发展趋势,互联网与保险进一步融合,人工智能、大数据、区块链等技术加速向保险行业渗透,保险业务的数字化转型正迸发出蓬勃生机。据统计,2018年前三季度,易安保险、众安保险、泰康在线、安心保险四大互联网保险公司,实现原保险保费收入64.64亿元,同比增长133.77%,远高于行业平均增速。回顾2018年,我们看到,互联网保险业务在行业创新和监管调试中稳步前行。

一、金融监管体制改革下的互联网保险监管

年初,保险行业监管格局发生变化。2018年3月召开的十三届全国人大一次会议审议并通过了《国务院机构改革方案》,该方案将中国银行业监督管理委员会和中国保险监督管理委员会的职责整合,组建中国银行保险监督管理委员会,其主要职责是,依照法律法规统一监督管理银行业和保险业,维护银行业和保险业合法、稳健运行,防范和化解金融风险,保护金融消费者合法权益,维护金融稳定。同时,将中国银行业监督管理委员会和中国保险监督管理委员会拟订银行业、保险业重要法律法规草案和审慎监管基本制度的职责划入中国人民银行。3月21日,中国银行保险监督管理委员会举行成立大会。8月,银保监会“三定”方案出炉,新的银保监会将设26个内设职能部门加机关党委,并设置**风险官、**检查官、**律师和**会计师。12月17日,银保监会下辖的36个省(自治区、直辖市、计划单列市)银保监局统一挂牌。

新成立的银保监会在监管理念和重点上有所调整。根据8月29日召开的银行保险监管工作电视电话会议,此次会议提出近期的工作重点中首要的就是继续做好防范化解金融风险各项工作,特别提出要自觉在互联网金融风险整治的框架下,发挥好银行保险监管部门职责,防控处置好互联网金融风险;积极防范、稳妥处置好其他重点领域、重点机构风险,牢牢守住不发生系统性金融风险的底线。

4月25日,中国银行保险监督管理委员会网站还发文提示了互联网保险的三大风险隐患——风险一是“吸睛”产品暗藏误导:有的保险机构为片面追求关注度和销售量,存在宣传内容不规范、网页所载格式条款的内容不一致或显示不全、未明确说明免责条款等问题,涉嫌误导消费者;风险二是在线平台暗藏“搭售”:某些在线平台在其票务、酒店预定页面通过默认勾选的方式销售一些保险产品,未明确列明承保主体或代理销售主体,未完整披露保险产品条款等相关重要信息。风险三是“高息”产品暗藏骗局:一些不法分子利用互联网平台虚构保险产品或保险项目,或承诺高额回报引诱消费者出资,或冒用保险机构名义伪造保单,往往涉嫌非法集资,给消费者造成经济损失。

二、互联网与保险进一步融合,数字化转型加速

2018年互联网头部企业继续加速布局保险业务,监管方也给予了相当的支持。2月24日,保监会批复美团点评实际控制的重庆金诚互诺保险经纪有限公司获得保险中介机构牌照。7月24日,银保监会批复同意了安联财产保险(中国)有限公司的增资方案,增资后北京京东叁佰陆拾度电子商务有限公司持股30%。这意味着京东拿到了一块财险保险牌照。11月2日,京东宣布,获中国银保监会批准,安联财产保险(中国)有限公司获准更名为京东安联财产保险公司,这也是继阿里、腾讯后第三家互联网巨头拿到了保险牌照。此外,百度、小米、美团、滴滴、今日头条、新浪、唯品会也在加速布局保险业务。同样值得注意的是,12月20日,香港保险业监管局向保泰人寿发出首张虚拟保险牌照。这家新型保险公司持有和使用全数码分销渠道,不涉及任何保险中介。

另一方面,保险服务的数字化转型升级也提上了监管方的日程。6月,有消息称,监管部门拟全面推进保险服务标准化制度建设,搭建标准化制度体系框架,《中国保险服务标准体系监管制度框架》已起草完毕,正在业内进行第二次征求意见。框架的总体目标包括推进保险服务数字化转型升级,加快数字保险建设,构建以数据为关键要素的数字保险,推动保险服务供给侧改革,更好服务我国经济社会发展和人民生活改善;框架的制度特征包括“数字化、网络化、智能化导向”的表述。此外,中国保险学会也联合业界成立了“保险智能风控实验室”,将全方位为保险反欺诈提供专业化、智能化的解决方案,利用AI手段解决国内保险风控的痛点,充分发挥大数据、人工智能、云计算等技术优势,为保险业欺诈风险的分析和预警监测提供支持。

三、将互联网保险纳入防范化解重大风险攻坚战,强化监督管理

防控互联网保险业务风险是2018年监管层的主要着力点。1月17日,保监会印发关于《打赢保险业防范化解重大风险攻坚战的总体方案》的通知,《方案》提出关注利用互联网技术推广的、影响客户信息安全的、互联网借贷相关的各类新型保险业务风险和财险公司、人身险公司、保险中介机构与第三方网络平台合作开展保险业务的风险隐患,要求采取有效措施汇总并评估各类互联网保险业务风险,以及非法开展互联网保险业务的风险;提出改进互联网保险监管制度,研究制定互联网创新型保险业务的监管制度。

新成立的银保监会延续了《方案》的部署。除了上述4月25日银保监会发布的《风险提示》外,6月4日,银保监会还发布了《关于2017年度保险业偿付能力监管工作情况的通报》,明确指出在发展互联网保险领域,银保监会将重点展开险企偿付能力真实性核查工作,加大查处力度,对造假公司采取严厉措施;此外,互联网保险产品在网络平台的销售过程中,涉嫌未明确说明免责条款、未完整披露保险产品条款、宣传内容不规范等问题,也将作为2018年金融监管部门整治的险企风险问题之一。同一日,银保监会下发了《关于加强自媒体保险营销宣传行为管理的通知》,要求各保险公司、保险中介机构提高对自媒体保险营销宣传行为管理重要性的认识,建立健全自媒体保险营销宣传行为管理制度,加强从业人员合规教育与职业道德教育。确保营销宣传信息合规准确,完善信息监控和处置机制,加大责任追究力度,落实监管责任。

在对互联网保险的具体监管和执法上,也贯穿了防范风险和从严监管的要求。*典型的是11月,两款“互联网+互助”保险产品被监管约谈,并被叫停。据其中一个产品参与方的披露,被叫停的原因是“涉嫌存在未按照规定使用经备案的保险条款和费率、销售过程中存在误导性宣传、信息披露不充分等问题。”在对互联网保险的执法方面,7月4日,浙江保监局网站上公布了两张有关互联网保险的罚单,剑指虚构部分技术服务费来支付推广费的违法行为等问题。而10月18日,银保监会对6家保险公司开出监管函,互联网保险公司占了其中一半。

四、健全完善互联网保险监管规范体系

互联网保险的稳健发展依赖于专门监管规则体系的建设。2015年,原中国保监会曾印发《互联网保险业务监管暂行办法》,作为互联网保险的基本依据,但根据原规定的施行期,该办法将于2018年10月到期失效。因此,2018年互联网保险监管规范体系建设逐步提速。9月30日,中国银保监会印发《中国银保监会关于继续加强互联网保险监管有关事项的通知》,表示正在加快《互联网保险业务监管暂行办法》的修订工作,在新的规定出台以前,原《暂行办法》继续有效。《通知》既肯定了《暂行办法》3年以来的规制价值,又面对新形势新问题对加强互联网保险监管提出要求。10月中旬,银保监会又对《互联网保险业务监管办法(草稿)》进行征求意见。征求意见稿放宽了保险公司、保险中介机构和保险公估机构经营互联网保险的区域限制;允许银行类保险兼业代理机构在其自营网络平台开展互联网保险业务;针对互联网保险信息披露和宣传方面做出详细规定;对第三方平台的资质、信用程度等方面提出了监管要求。

针对互联网时代保险业务的新特点,今年银保监会还着手制定保险实名登记管理和保险销售行为可回溯管理的有关制度并征求意见。其中《保险实名登记管理办法》的征求意见稿明确,保险实名登记,是指包括第三方网络平台在内的机构及其从业人员在为投保人、被保险人、受益人办理保险业务时,依照本办法要求核对身份证件,并查验和登记实名信息的行为。银保监会建立保险实名查验登记平台,用于保险实名信息查验、登记和保险账户管理。银保监会委托、指导第三方机构承担保险实名查验登记平台的建设和运行管理。对于存在严重违法失信行为的,将其列入联合惩戒对象,实施联合惩戒。如存在使用虚假身份证件、冒用他人名义、提供虚假信息等行为的,将被纳入失信行为记录名单。

根据2017年出台的《保险销售行为可回溯管理暂行办法》,保险公司、保险中介机构开展互联网保险业务,依照中国保监会互联网保险业务监管的有关规定开展可回溯管理。今年7月,银保监会下发《关于规范互联网保险销售行为可回溯管理有关事项的通知(征求意见稿)》,明确规定:“保险机构通过第三方网络平台开展互联网保险销售的,应在第三方网络平台单独设置说明所售产品为保险和投保意愿确认界面,由投保人主动确认后进入保险机构自营平台投保流程。”根据该征求意见稿,互联网保险销售行为可回溯管理涵盖销售界面管理和销售过程记录两项。其中,前者指保险机构应保存销售过程中关键销售界面的内容信息及历史修改信息,建立版本管理机制;后者指保险机构应保存销售过程中客户投保信息、操作平台、操作轨迹、操作时间,以及保险机构收到或传递投保人投保申请的时间。

--本文源自京东数字科技研究院

暂无评论!
我要评论 只有购买过该商品的用户才能评论。

Gotham Therapeutics Establishes Advanced Oncology Profiling Cascade with ProQinase to Progress its Portfolio of Epitranscriptomic Drug CandidatesWEDNESDAY, OCTOBER 30, 2019Gotham Therapeutics, a biotechnology company developing a novel drug class targeting RNA-modifying proteins, and ProQinase, an early stage drug-discovery company, recently acquired by Malvern/PA-based Reaction Biology Corp., today announced that they have established an array of advanced biochemical and cellular assays to characterize epitranscriptomic-directed compounds.“Establishing tailored target engagement, cell biology, phenotypic, and in-vivo assays to evaluate compounds originating from our three most advanced epitranscriptomic programs in parallel is a crucial next step to develop our broad pipeline towards the clinic,” said Dr. Gerhard Müller, Chief Scientific Officer of Gotham Therapeutics. “By pursuing the full range of the reader-writer-eraser continuum, we are able to focus on targets with the most compelling links to disease and advance those programs in tandem.”“Combining our high proficiency in providing customized solutions as early stage drug-discovery services, including tailor-made biochemical and cell-based assays, with Gotham’s expertise in epitranscriptomics, we were able to establish in a very short time a set of customized enzymatic and cellular assays for compounds addressing three different mRNA-modifying targets,” said Dr. Sebastian Dempe, Chief Executive Officer of ProQinase. “We look forward to supporting Gotham as the company advances its programs into lead optimization and to continued work with the Gotham team assisting the company to advance its broad pipeline in a time-effective manner.”In addition to establishing a tailor-made profiling cascade for compounds from its three most advanced programs, Gotham has also made progress in strengthening its drug discovery engine and developing its candidate base. Gotham previously completed the gene-to-lead phase for its drug discovery project targeting the METTL3/METTL14 complex and established a robust discovery process as a platform for future projects. The company has also generated a library of high-quality compounds tailor-made for accelerated hit generation and hit-to-lead expansion against large parts of the epitranscriptomic target space. This library includes a collection of over 2,000 analogues covering over 80 distinct chemotypes that will be used to further accelerate Gotham’s drug discovery efforts as it expands its pipeline.The original link:https://www.pharmafocusasia.com/news/gotham-therapeutics-establishes-advanced-oncology-profiling-cascade-with-proqinase-to-progress-its-portfolio-of-epitranscriptomic-drug-candidates2019 Asia-pacific pharma IP Leader Summit: http://en.zenseegroup.com/p/510934/will be held in Beijing  on November 14-15, and will attract more than 500 industry experts from domestic and foreign pharmaceutical companies, biotechnology companies, governments, associations, law firms, intellectual property agents and other companies to attend.Official registration and consultation channels:Contact:AnnPhone: 021-65650305Email:Marketing@zenseegroup.comhttp://en.zenseegroup.com/p/510934

Gilead and Glympse Bio Announce Strategic Collaboration for Use of Biomarker Technology in NASH Clinical DevelopmentTUESDAY, OCTOBER 29, 2019Gilead Sciences Inc. and Glympse Bio, Inc., today announced that the companies have entered into a strategic collaboration in nonalcoholic steatohepatitis (NASH) clinical development. Glympse Bio’s proprietary synthetic biomarkers – bioengineered to identify stage and progression of disease as well as early detection of treatment response – will be used to determine clinical trial participants’ stage of disease at initial screening and to determine responses to study treatment in Gilead’s NASH clinical program.“We are excited about the opportunity to partner with Glympse Bio to help inform our NASH development program,” said Mani Subramanian, MD, PhD Senior Vice President, Liver Diseases, Gilead Sciences. “By utilizing this innovative technology, we hope to better characterize this complex disease and improve our understanding of how our compounds impact disease progression.”Glympse Bio’s proprietary technology, Glympse Inside™, combines synthetic biomarkers with machine learning approaches to identify the stage and monitor progression of important, complex diseases such as cancer, fibrosis, inflammation, and infections, in real time.“We are very excited about partnering with Gilead, a leader in drug development, to help drive earlier and more favorable outcomes for patients,” said Caroline J Loew, President and CEO, Glympse Bio. “Gilead’s commitment to developing innovative medicines in areas of high unmet medical need aligns with our mission of transforming disease detection and measuring treatment response, all with the goal of helping improve the lives of patients.”information source:pharma focus AsiaThe original link:https:https:https://www.pharmafocusasia.com/news/gilead-and-glympse-bio-announce-strategic-collaboration-for-use-of-biomarker-technology-in-nash-clinical-development2019 Asia-pacific pharma IP Leader Summit:http://en.zenseegroup.com/p/510934/ will be held in Beijing  on November 14-15, and will attract more than 500 industry experts from domestic and foreign pharmaceutical companies, biotechnology companies, governments, associations, law firms, intellectual property agents and other companies to attend.Official registration and consultation channels:Contact:AnnPhone: 021-65650305Email:Marketing@zenseegroup.comhttp://en.zenseegroup.com/p/510934

HistoIndex Announces Global Partnerships To Expand AI-Based Digital Pathology PlatformMONDAY, OCTOBER 28, 2019HistoIndex announces the expansion of its AI-based digital pathology platform towards large-scale NASH preclinical programs for pharmaceutical and biotech companies to achieve quantifiable and reproducible data on therapeutic responses in NASH animal models, and to aid CROs as well as research agencies in validating new models mimicking the NASH disease.Published preclinical studies have demonstrated the use of HistoIndex's fully quantifiable Second Harmonic Generation (SHG) technology as a highly accurate stain-free method that can monitor the efficacy of various therapeutic agents, by quantifying more than 450 NASH-associated parameters in fibrosis, inflammation, ballooning and steatosis. The information of these NASH-associated parameters gathered from the entire liver tissue, provides comprehensive insights on the mechanism of action of the therapeutic agent.  As a drug discovery tool, HistoIndex's SHG-enabled digital pathology platform will allow pharmaceutical and biotech companies to select promising lead candidates for further optimization and make informed decisions in the management of their NASH drug development pipeline.In addition to ongoing NASH clinical trials, HistoIndex is currently involved in multiple preclinical studies, most of which are conducted by major pharmaceutical and biotech companies, medical universities, CROs and research agencies. Notably, HistoIndex has recently entered into a collaboration with the A*STAR's Genome Institute of Singapore (GIS) to validate their in vivo and in vitro NASH models based on Asian-centric clinical data. Says Professor Patrick Tan, Executive Director of the Genome Institute of Singapore (GIS), "At GIS, we conduct our preclinical studies on fatty liver involving data from animal models based on patient-derived transcriptomic data. This has a high translational potential as it helps us to pinpoint new therapeutic targets and their validation. Therefore, using a fully quantitative, reliable and objective pathological evaluation such as HistoIndex's AI-based digital pathology platform is essential to the success of our efforts in therapeutic target discovery."HistoIndex is also a partner with globally-renowned CRO, WuXi Apptec, in advancing their NASH preclinical programs with advanced R&D and smart imaging analysis capabilities. Published study data will be available for discussions during networking opportunities throughout AASLD's The Liver Meeting® in November 2019.  "We are very excited to extend our AI-based SHG platform to preclinical studies to help companies with drug discovery programs select promising lead candidates for further optimization and subsequent clinical development," says Dr Poon Thong Yuen, Chief Executive Officer of HistoIndex. "Our SHG image analysis platform has already been used to analyze the efficacy of a series of promising drug candidates for NASH within various animal models commonly-used by the industry, and we believe these preclinical partnerships will help drive the adoption of our platform significantly."information source:pharma focus AsiaThe original link:https:https://www.pharmafocusasia.com/news/histoindex-announces-global-partnerships-to-expand-ai-based-digital-pathology-platform2019 Asia-pacific pharma IP Leader Summit: http://en.zenseegroup.com/p/510934/will be held in Beijing  on November 14-15, and will attract more than 500 industry experts from domestic and foreign pharmaceutical companies, biotechnology companies, governments, associations, law firms, intellectual property agents and other companies to attend.Official registration and consultation channels:Contact:AnnPhone: 021-65650305Email:Marketing@zenseegroup.comhttp://en.zenseegroup.com/p/510934

AVROBIO Receives Orphan-Drug Designation from the U.S. FDA for AVR‑RD‑02 for the Treatment of Gaucher DiseaseFRIDAY, OCTOBER 25, 2019AVROBIO, Inc., today announced that the U.S. Food and Drug Administration (FDA) has granted orphan-drug designation for the Company’s investigational gene therapy, AVR-RD-02, for the treatment of Gaucher disease. AVR-RD-02 consists of the patient’s own hematopoietic stem cells, genetically modified to express glucocerebrosidase (GCase), the enzyme that is deficient in Gaucher disease. The Company is actively recruiting in Canada for its Phase 1/2 clinical trial of AVR-RD-02, which seeks to evaluate the safety and efficacy of the therapy in patients with Type 1 Gaucher disease.“Under the existing standard of care, patients with Gaucher disease are bound to a lifelong infusion schedule of enzyme replacement therapies, and still experience painful and progressive symptoms such as debilitating musculoskeletal pain and fatigue,” said Birgitte Volck, MD, PhD, President of Research and Development at AVROBIO. “Orphan-drug designation recognizes the unmet need of populations with rare diseases like Gaucher where AVROBIO strives to transform lives by addressing the underlying cause of the disease with a single dose of gene therapy.”Orphan-drug designation is granted by the FDA to drugs and biologics which are intended for the safe and effective treatment, diagnosis or prevention of rare diseases or conditions that affect fewer than 200,000 people in the United States. Orphan-drug designation provides certain incentives, which may include tax credits towards the cost of clinical trials and prescription drug user fee waivers.information source:pharma focus AsiaThe original link:https:https://www.pharmafocusasia.com/news/avrobio-receives-orphan-drug-designation-from-the-us-fda-for-avrrd02-for-the-treatment-of-gaucher-disease2019 Asia-pacific pharma IP Leader Summit: http://en.zenseegroup.com/p/510934/will be held in Beijing  on November 14-15, and will attract more than 500 industry experts from domestic and foreign pharmaceutical companies, biotechnology companies, governments, associations, law firms, intellectual property agents and other companies to attend.Official registration and consultation channels:Contact:AnnPhone: 021-65650305Email:Marketing@zenseegroup.comhttp://en.zenseegroup.com/p/510934

FRIDAY, OCTOBER 25, 2019AZTherapies, Inc., a biopharmaceutical company developing therapeutics to extend brain health, today announced the acquisition of Smith Therapeutics, a private biopharmaceutical company with a shared goal of targeting neuroinflammation to treat neurodegenerative disease. Smith Therapeutics’ Founder and Chief Executive Officer Philip Ashton-Rickardt, Ph.D., has joined the senior leadership team at AZTherapies as Senior Vice President of Immunology. Financial terms of the acquisition were not disclosed.Smith Therapeutics’ proprietary research platform focuses on the use of modified T cells to restore a healthy balance of inflammatory and regulatory cells in the brain. To date, Smith has successfully engineered immunosuppressive T regulatory (Treg) cells with Chimeric Antigen Receptors (CARs) targeting brain glial cells. Previous research has demonstrated the ability of Tregs to dampen microglial activity and reduce neuroinflammation in models of neurodegeneration, suggesting their potential utility in the treatment of diseases including Progressive Supranuclear Palsy (PSP), Alzheimer’s disease, Parkinson’s disease, Huntington’s disease, Amyotrophic Lateral Sclerosis (ALS), and others.“This acquisition represents a meaningful step forward for us as we continue to strengthen our leadership position in the development of therapies targeting neuroinflammation to stop or slow the progression of neurodegenerative diseases,” said David R. Elmaleh, Ph.D., Founder, CEO, and Chairman of AZTherapies. “We are excited to be working with Philip as we add this cutting-edge technology to our portfolio of innovative programs. An esteemed immunologist and inventor of the technology, Philip brings unparalleled expertise to the company and we look forward to advancing this CAR-Treg program further into IND-enabling studies and into clinical development as rapidly as possible.”Dr. Ashton-Rickardt commented on the acquisition and his appointment: “Our shared rationale of targeting neuroinflammation as the root cause of neurodegenerative disease makes this acquisition a great strategic fit for us. With AZTherapies’ expertise in drug development and clinical trial execution, we believe that together, we are well positioned to advance our CAR-Treg technology and fundamentally change neurodegenerative disease progression.”Prior to launching Smith Therapeutics in 2017, Dr. Ashton-Rickardt was Chair in Immunology at Imperial College London, Visiting Professor, Brigham and Women’s Hospital, Harvard Medical School, and Associate Professor in the Department of Pathology at the University of Chicago. His work has been recognized by his peers through the award of tenure from The University of Chicago and by his fellow citizens as a recipient of the Early Career Award for Scientists and Engineers from President Bill Clinton. He has published more than 65 peer-reviewed papers in more than 30 academic journals (including Cell, Science, Immunity, and Nature Immunology), has served as an editor for several academic journals, and has been a member of grant review boards globally. Dr. Ashton-Rickardt received a B.Sc. in Biochemistry from the University of London, King’s College with honors, a Ph.D. in Molecular Biology from the University of Edinburgh, and completed post-doctoral work at the University of Edinburgh and the Massachusetts Institute of Technology in Molecular Biology and Molecular Immunology, respectively.information source:pharma focus AsiaThe original link:https:https://www.pharmafocusasia.com/news/aztherapies-strengthens-neuroinflammation-targeted-pipeline-through-acquisition-of-smith-therapeutics2019 Asia-pacific pharma IP Leader Summit: http://en.zenseegroup.com/p/510934/will be held in Beijing  on November 14-15, and will attract more than 500 industry experts from domestic and foreign pharmaceutical companies, biotechnology companies, governments, associations, law firms, intellectual property agents and other companies to attend.Official registration and consultation channels:Contact:AnnPhone: 021-65650305Email:Marketing@zenseegroup.comhttp://en.zenseegroup.com/p/510934

About Us
Contact Us
Zensee_Daystar online