RDPAC-助力健康中国

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</script> <div class="row" style="margin-bottom: -5px;"> <div class="col-lg-12 video_play" style="position: relative;padding:0!important;"> <img src="/images/video_bg.jpg" style="width:100%;height:auto;" > <a href="javascript:void(0);" onclick="videoStart();" style="position:absolute;top:40%;width:100%;text-align: center;left:0;opacity: .5;" ><img src="/images/chuang7.png" class="play_btn" ></a> </div> <div class="col-lg-12 hidden" id="videoPlay" style="padding:0!important;"> <video src="/video/rdpac_blue.mp4" id="videoplayer" controls="controls" style="width: 100%;"> </video> </div> </div> <div style="width:100%;background: #313e4e;" id="innovation"> <div class="container" style="background: #313e4e"> <div class="row"> <div class="col-lg-8" style="padding-bottom: 10rem;"> <h1 style="color:#fff;padding-top:10rem;font-size:40px;">研发与创新</h1> <div style="color:#fff;line-height: 40px;"> <p style="line-height: 1.5em;">创新驱动发展是国家“十三五”的核心战略，而医药产业是创新的支柱产业之一。医药创新不仅可为经济发展提供长久动力，同时也是解决民生问题的根本要求。近年开展的药品审评审批制度改革，通过一系列国家级政策措施，包括优化审评审批体系、提高审评能力与效率、加强国际协调和一致性等，促进和鼓励医药创新，提高上市药品质量。</p><p><br/></p><p style="line-height: 1.5em;">我们致力于成为政府坚实的合作伙伴，与会员公司形成合力，共同支持药监部门，加强产学研沟通合作，加强早期研发各参与方的协作，促进临床研究能力建设。支持中国建立国际化的、基于科学的、透明的和可预测的监管框架体系，最大程度释放中国的创新潜力，加速创新药在中国上市，提高患者创新药物可及性，在全球创新体系下造福全球患者。</p> </div> </div> <div class="col-lg-4" style="overflow: hidden"> <img src="/images/z1.jpg" > </div> </div> </div> </div> <div class="row" id="drug"> <div class="col-lg-12" style="background: url(/images/z2.jpg) center center no-repeat;background-size: cover;"> <div class="container" style="padding: 13rem 0;"> <h1 style="color:#333;font-size:40px;">药品质量与安全</h1> <p style="line-height: 1.5em;">为深入贯彻《药品管理法》中“保证药品质量，保障公众用药安全和合法权益，保护和促进公众健康”宗旨， RDPAC愿意与作为中国制药行业质量管理标杆企业的会员公司一起，分享全球先进的药品生产管理经验，全生命周期质量管理体系，积极参与医药政策的落地实施及配套法规的献言建策，在上市许可持有人制度下支持上市后药品监管，为患者获得高质量的、安全有效的药品而努力。</p> </div> </div> </div> <div class="row" id="access"> <div class="col-lg-12" style="background: #fff;"> <div class="container" style="padding: 13rem 0;"> <h1 style="color:#333;line-height: 50px;margin-bottom:40px;font-size:40px;">药物可及</h1> <p style="line-height: 1.5em;">我们作为政府和产业间的桥梁纽带，长期促进引导企业与政府的沟通配合，结合国际先行经验和本土实践开展学术研究，在药品价值评估，药品采购供应，以及支付方式改革等医改重点优先任务方面积极建言献策。我们将携会员公司和各界共同努力，助力政府全面建成高质量、多层次、可持续的全民医疗保障体系，让中国的老百姓早日“用得上、用得起”好药新药。</p><p><br/></p><p style="line-height: 1.5em;">建立健全、可持续的药品价格形成和报销政策框架，提高创新和高质量药物患者可及性，将促进药品创新的政策生态体系的发展，进一步改善人民的健康状况，并使《“健康中国2030”规划纲要》的最终目标得以实现。</p><p><br/></p><p style="line-height: 1.5em;">RDPAC携手行业伙伴，共同研究并设计了一个循证、可持续的创新药物价格形成机制和医保报销政策框架，以期实现如下目标： </p><ul class=" list-paddingleft-2" style="list-style-type: disc;"><li><p style="line-height: 1.5em;">提高我国患者对创新药物和优质药物的可及性，减轻患者经济负担，提高我国人民的健康水平； </p></li><li><p style="line-height: 1.5em;">优化医疗资源的分配和利用，鼓励医生和监管方重回以患者需求为中心，并奖励具有高临床价值的药品； </p></li><li><p style="line-height: 1.5em;">鼓励发展具有持续创新力的生态系统，增强国家竞争力。</p></li></ul><p><br/></p> <a href="http://cnadmin.rdpac.org/upload/upload_file/1575476742.pdf" style="display:block;margin-top:40px;color:#116CAF;font-style: italic;font-size:2rem;text-decoration: underline;">《提高创新药物可及性助力健康中国》报告全文下载</a> </div> </div> </div> <div class="row" id="ipr"> <div class="col-lg-7" style="background: url(/images/z3.jpg) left top no-repeat;background-size: cover;min-height:84rem;"> <h1 style="color:#fff;font-size:40px;float:right;margin-top:38rem;margin-right: 40px;">知识产权保护</h1> </div> <div class="col-lg-5"> <div style="color:#333;line-height:40px;width:100%;box-sizing: border-box;padding:10rem 8rem 10rem 4rem;"> <p style="line-height: 1.5em;">加强药物知识产权保护、倡导药物创新，不仅能为中国研发制药行业发展提供有效的激励，更是确保中国患者尽早获得创新、安全药品的根本保障。由于创新药研发的高投入、高风险、长周期等特性，知识产权保护是创新性产业的根基，对于医药产业的可持续发展尤为重要。我们建议从专利申请、数据保护执行、完善专利链接制度和建立专利期延长制度四个方面着手，发挥知识产权保护对医药创新的激励作用。</p> </div> </div> </div> <div style="width:100%;background: url(/images/z5.jpg) left top no-repeat;background-size: cover;" id="business"> <div class="container" style=""> <div class="row"> <div class="col-lg-12" style="padding-bottom: 15rem;"> <h1 style="color:#fff;padding-top:15rem;font-size: 40px">良好商业道德</h1> <div style="color:#fff;line-height: 40px;font-size:24px;"> <p style="line-height: 1.5em;">自2013年起，RDPAC联合国内行业协会致力于推广《医药企业伦理准则》。至2015年，已有17家行业协会、商会签署了实施《医药企业伦理准则》倡议书，要求医药界同仁遵循《伦理准则》中以医疗健康和患者为中心、诚信、独立、合法、透明和责任的六大原则，自觉遵守《伦理准则》各项条款，并呼吁政府继续强化改革、依法行政、扬善惩恶、净化市场，共同助力规范中国医药市场秩序，为大众营造一个健康、有序的医疗保健环境。</p><p><br/></p><p style="line-height: 1.5em;">2018年，来自全国的25家制药及医疗器械领域的协会和商会、医疗卫生领域专业人士相关协会共同签署了《中国制药及医疗器械领域伦理合作共识框架》这是自2013年行业联合推行合规建设以来，第一次将参与机构扩展至医院行业组织，及省市级医药行业协会。这也标志着制药、医疗器械以及医疗卫生专业人士在《共识框架》下正式广泛联合，共同规范落实高标准的道德实践标准，加强医药和医疗器械生产销售企业、相关行业协会、医疗卫生专业人士和政府机关之间的交流，从而促进全民医疗事业的发展。</p> </div> </div> </div> </div> </div> <script> function videoStart() { $("#videoPlay").removeClass('hidden'); 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