FDA
The U.S. Food and Drug Administration regulates drugs, biologics, medical devices, diagnostics, and certain software products.
A working glossary for healthcare-system, regulatory, payment, and market-access terms used throughout the site.
The U.S. Food and Drug Administration regulates drugs, biologics, medical devices, diagnostics, and certain software products.
The National Medical Products Administration is China’s primary regulator for drugs and medical devices.
The National Healthcare Security Administration is central to China’s insurance, pricing, reimbursement, and procurement reforms.
The National Health Commission oversees major health policy, public health, hospitals, and system administration.
Coverage refers to whether a payer will pay for a service or product under defined circumstances.
Reimbursement refers to payment for a covered service or product, including amount, billing pathway, and payer rules.
A Chinese centralized purchasing policy that uses purchase volume commitments to reduce prices for selected drugs or devices.
A regulated Chinese model for online healthcare services connected to licensed medical institutions.
The broad public insurance structure that finances much of covered medical care in China, with local benefit variation.
A county-level hospital that anchors local access and connects rural patients to higher-level referral systems.
An organizational linkage among hospitals and lower-level providers intended to improve coordination and tiered care.
A contracted primary-care model intended to improve continuity, prevention, and chronic disease management.
The development of digital systems for hospitals, public health, insurance, administration, and regional platforms.
The portion of healthcare cost paid directly by households rather than by insurance or government funding.
A high-level hospital category associated with advanced care, referral capacity, specialists, and institutional prestige.
A top-grade hospital classification often used as shorthand for elite hospital status, though specialty strength still varies.
A formal evaluation process tied to hospital capability, quality systems, management, and classification.
A network arrangement linking higher-level hospitals with lower-level facilities to support referral and capacity building.
The administrative, financial, clinical, and policy structure that shapes public hospital behavior.
A hospital with major teaching, research, and advanced-care functions, often linked to a university or medical college.
A hospital that receives patients from lower-level facilities or broader regions for more complex care.
A hospital organized around a disease area, patient population, medical discipline, or clinical service line.
A structural page explaining an institution’s role rather than a current rating or quality endorsement.
The trust a product, service, or care model gains from use or support by respected clinical institutions or experts.
A profile format that explains how a city functions as a healthcare node, including hospitals, referral patterns, and regional role.
A hospital or city that receives patients from a broader region for more complex care.
The healthcare delivery, public-health, provider, and administrative environment within a municipality or city.
A group of hospitals connected to a university or medical school that may influence teaching, research, and clinical practice.
The process of assessing whether a product or service can gain adoption within a city, province, or regional healthcare market.
A page that explains a province as a healthcare geography, including anchor cities, hospitals, access constraints, and policy implementation.
A page that explains a multi-province area such as western China, the Greater Bay Area, or the Yangtze River Delta.
A city that organizes regional healthcare capacity through major hospitals, universities, referral flows, and administrative influence.
Variation in access, capacity, affordability, or outcomes across provinces, cities, rural areas, and remote regions.
A region where healthcare activity is shaped by adjacent jurisdictions, travel, policy coordination, or institutional exchange.
The broad public medical insurance system that finances much of covered care in China, with local variation in benefits and reimbursement.
Urban Employee Basic Medical Insurance, an employment-linked basic medical insurance arrangement.
Urban Resident Basic Medical Insurance, a legacy resident coverage category important to reform history.
New Rural Cooperative Medical Scheme, a legacy rural coverage program central to rural insurance expansion.
National Reimbursement Drug List, the key reimbursement list for medicines under basic medical insurance.
National Healthcare Security Administration, the agency central to insurance, payment, pricing, and procurement reform.
Locally sponsored or city-linked supplemental insurance designed to fill selected gaps in basic coverage.
A purchasing mechanism that links committed volume to lower prices for selected drugs, devices, or consumables.
A payment method that groups cases by diagnosis-related categories to constrain open-ended fee-for-service incentives.
A Chinese payment reform using data-driven diagnosis-intervention packets and point-based local fund management.
A distribution reform intended to reduce intermediary layers and markups in pharmaceutical distribution.
Device and consumable categories, such as implants or procedure-linked products, that can be subject to procurement pressure.
A reform that removed hospital drug markups and forced compensation and service-pricing changes.
Community-based rural health workers associated with Mao-era cooperative medicine and basic rural care.
Mass public-health mobilization campaigns focused on sanitation, prevention, vector control, and local participation.
A formalized field of practice, education, hospitals, products, regulation, and cultural identity in China.
A state-recognized medical institution organized around Traditional Chinese Medicine services, often within modern hospital infrastructure.
A TCM practice and product category involving formulas, prepared products, raw materials, quality control, and regulation.
A TCM-associated practice used in China and internationally, with evidence and policy debates varying by condition and setting.
A long-duration condition requiring prevention, monitoring, medication management, follow-up, and often coordination between primary and specialty care.
The population-level impact of illness, disability, death, and care needs, often used to connect epidemiology with health-system priorities.
Deaths related to pregnancy or childbirth, used as an indicator of maternal health and system capacity.
Deaths among infants, used as an indicator of child health, neonatal care, public health, and social conditions.
Heart and vascular disease, including conditions that require prevention, acute care, procedures, rehabilitation, and long-term management.
The systematic collection and use of health data for disease control, outbreak response, and population-health management.
Functional, social, and medical support for people with sustained care needs due to aging, disability, illness, or frailty.
China’s household registration system, which can affect access to public services, insurance administration, and local benefits.
Financial hardship or impoverishment caused by illness costs despite insurance or assistance.
Severe or high-cost illness that can expose the limits of insurance coverage and household financial resilience.
Children remaining in their home communities while one or both parents migrate for work.
A medicine intended for a rare disease, requiring separate analysis of approval, pricing, reimbursement, and access.
A federal U.S. health insurance program primarily serving older adults and selected disabled populations.
A joint state-federal U.S. program covering low-income and medically vulnerable populations, with substantial state variation.
Health insurance offered through employment and a central coverage source for working-age Americans.
Private-plan Medicare coverage administered by contracted plans using managed-care tools.
An intermediary that administers prescription drug benefits, formulary design, pharmacy networks, and rebate arrangements.
A utilization management process requiring payer approval before selected services, drugs, devices, or procedures are covered.
A method that compares institutions, incentives, financing, regulation, and patient pathways rather than country labels alone.
A useful shorthand for U.S. healthcare’s multiple payer, provider, regulatory, and contractual structures.
A useful shorthand for Chinese healthcare policy, where central direction is translated through provincial, municipal, and hospital-level implementation.
The chain from regulatory permission to payment, procurement, adoption, and patient access.
A requirement or policy pressure that keeps certain data processing, storage, transfer, or governance within a jurisdiction.
The rules and institutions governing clinical AI safety, data use, validation, deployment, monitoring, and accountability.
The U.S. Food and Drug Administration, the federal agency regulating drugs, biologics, medical devices, diagnostics, and certain software-based medical products.
China’s National Medical Products Administration, the agency responsible for regulating drugs, medical devices, cosmetics, and related product registration.
Software intended for one or more medical purposes that performs those purposes without being part of a hardware medical device.
Clinical evidence about product use and outcomes derived from analysis of real-world data, subject to fit-for-purpose quality tests.
The system for detecting, assessing, understanding, and preventing adverse drug reactions and related drug safety risks.
Lifecycle monitoring after approval or registration, including adverse event reporting, signal detection, field action, and benefit-risk management.
The adaptation of a global regulatory dossier, claim, evidence plan, labeling, data strategy, and postmarket system to local regulatory requirements.
The pharmacologically active component of a medicine, distinct from excipients, packaging, and finished-dose formulation.
A contract development and manufacturing organization that provides development, manufacturing, analytical, or supply services for life-sciences companies.
A contract research organization that supports clinical trials, regulatory submissions, data management, monitoring, and development operations.
A biological product that is highly similar to an approved reference biologic, requiring comparability evidence rather than ordinary generic-drug logic.
A drug market-access strategy built around China’s National Reimbursement Drug List, price negotiation, patient affordability, and hospital access.
The controlled movement of process know-how, data, methods, biological materials, software, or manufacturing capability between organizations.
Costly, procedure-linked medical devices or materials, such as implants or specialist-use products, that are often exposed to procurement reform.
A diagnostic test performed on specimens taken from the human body, such as blood, tissue, or other samples.
Diagnostic testing performed near the patient or clinical decision point rather than in a central laboratory.
The use of scanned pathology slides, image-management systems, and related software for pathology review, consultation, or analysis.
A laboratory that receives specimens from other providers for specialized or centralized testing.
A channel partner that supports hospital access, logistics, tendering, service coordination, or sales for medical devices.
A regulated China-specific online medical institution model, often linked to physical hospitals or platform-based healthcare services.
A software-based intervention intended to treat or manage a disease or condition, requiring clinical evidence and a payment pathway.
The collection and review of patient health data outside traditional care settings, usually requiring a care-management workflow.
A U.S. policy concept involving practices that interfere with access, exchange, or use of electronic health information except as permitted by law or regulation.
The ability of health data systems to exchange and use information meaningfully across organizations, platforms, and care settings.
Health-related data that move or are accessed across jurisdictions, creating privacy, security, localization, consent, and governance risks.
The pathway by which a product moves from approval or availability to practical use through payment, procurement, hospital access, and adoption.
A procurement process in which qualified suppliers compete under specified purchasing, price, quality, or volume rules.
A structured approach to legitimate engagement with scientific, clinical, or institutional experts who influence evidence, training, and adoption.
The adaptation of product claims, evidence, service, data architecture, manufacturing, price, and commercial model to local market conditions.
A structured assessment of market attractiveness, adoption barriers, competitive position, payment route, channel feasibility, and execution risk.
The ordering of classification, evidence, submission, partner, data, reimbursement, and channel decisions to avoid rework and weak approvals.
The degree to which a product claim, evidence package, quality system, documentation, labeling, and postmarket plan are prepared for FDA interaction.
A code set used to identify medical services and procedures, especially physician and other professional services.
A coding system used by Medicare and other payers that includes CPT codes and additional codes for products, supplies, and services.
The plan for obtaining payer recognition that a product or service is medically necessary and payable for specified patients or indications.
A hospital committee or process that evaluates new products for clinical, operational, safety, supply-chain, and economic value.
The service, complaint handling, training, quality, reporting, repair, and customer-success infrastructure after product launch.
China’s central health administration body with major roles in health planning, delivery-system policy, public health, and medical service administration.
China’s regulator for drugs, medical devices, diagnostics, cosmetics, and related product registration and postmarket regulation.
China’s public-health institution for disease prevention, surveillance, technical guidance, public-health research, and outbreak-related functions.
A broad national health strategy framing long-term prevention, health promotion, public health, delivery reform, and population-health priorities.
China’s Personal Information Protection Law, a major personal-information governance law with important implications for health data.
An evidence process that evaluates clinical, economic, budget, and implementation value to inform reimbursement, pricing, procurement, or policy decisions.
Policy efforts to change public hospital incentives through pricing, payment, procurement, compensation, governance, and quality reforms.
Private care targeted to affluent, expatriate, employer-covered, or internationally insured patients seeking convenience, service quality, or specialist access.
A private or premium hospital segment oriented toward foreign-facing, multilingual, internationally insured, or high-service-standard care.
A preventive screening and health-assessment business model often tied to employer benefits, private pay, and diagnostic packages.
A planning framework for developing a specialty area such as oncology, cardiology, diabetes, rehabilitation, ophthalmology, or dental care.
A strategy for working with commercial insurers or supplemental payers rather than relying only on basic medical insurance.
支付方是否愿意在特定条件下支付某项医疗服务、产品或药品。
实际支付路径和支付金额,包括谁收款、收多少、在哪种服务场景下收。
美国医疗服务和程序编码体系中的核心代码体系之一,常用于描述专业服务和程序。
美国医疗编码体系之一,常用于 Medicare 和其他支付流程中的产品、供应品和服务识别。
支付方要求某些服务、药品、检查或器械在支付前先获批准的使用管理机制。
美国医院评估新产品临床、运营、供应链和经济价值的采购相关机制。
美国诊断编码语境中常用的 ICD-10 临床修订版本,用于描述诊断和医学必要性背景。
诊断相关组,用于住院病例分组和支付或管理分析。
Pharmacy Benefit Manager,管理处方药福利、formulary、返点、药房网络和使用管理的中介机构。
面向新兴技术、服务和程序的临时代码,不自动代表成熟支付。
Medicare 是否在特定条件下覆盖服务或产品,可能涉及 NCD、LCD 和合理必要性标准。
医院对新产品的临床、经济、运营、供应链和风险价值进行评估的流程。
These pages explain how the site evaluates sources, weighs evidence, uses official data, maintains terminology, supports Chinese-language readers, and preserves historical material.
A category of evidence source, such as official agency material, administrative data, peer-reviewed literature, field evidence, or strategic inference.
A practical confidence label based on the type of source supporting a claim and the decision it is meant to inform.
A policy of retaining historical pages while keeping them separate from current guidance.
A selective simplified Chinese explanation layer for high-value cross-border topics rather than a full mirror of the English site.
These pages provide concise entry points into system, hospital, province, insurance, reform, TCM, population health, medtech, biopharma, digital health, market entry, regulatory, Chinese reader, FAQ, agency, and timeline topics.
A navigation page that groups related pages by decision problem rather than by alphabetical order.
A site index that groups system-level U.S., China, and comparative healthcare pages.
A site index for cross-border commercialization, reimbursement, procurement, partner, and readiness pages.
A site index for FDA, NMPA, clinical trial, drug, device, diagnostic, postmarket, and evidence pathway pages.
A page structure used to correct false equivalences and common interpretation errors.
A chronological orientation page that links historical developments to current analytical clusters.