China Cardiovascular Drug Market is at around $11.12 Bn in 2022 and is projected to reach $16.81 Bn in 2030, exhibiting a CAGR of 3.8% during the forecast period. The adoption of digital healthcare is a key factor driving the rise of the China Cardiovascular Drugs Market. The market is dominated by key players like Shanghai Fosun Pharmaceutical Group Co., Ltd., Jiangsu Hengrui Medicine Co., Ltd., Pfizer Inc., Bayer AG, Janssen Pharmaceuticals, Inc., AstraZeneca, Sanofi, Novartis, and Merck & Co., Inc.
China Cardiovascular Drug Market is at around $11.12 Bn in 2022 and is projected to reach $16.81 Bn in 2030, exhibiting a CAGR of 3.8% during the forecast period.
Heart and blood vessel illnesses are collectively referred to as cardiovascular diseases. These comprise deep vein thrombosis, pulmonary embolism, congenital heart disease, peripheral artery disease, rheumatic heart disease, and coronary heart disease. The three main groups of drugs used to treat heart-related problems are ACE inhibitors (like ramipril), antiarrhythmics (like amiodarone), and angiotensin-II antagonists (like losartan).
China has a socialist market economy, meaning that the vast majority of the economy is made up of state-owned businesses. The open-market economy that relies on supply and demand underpins the operations of the state-owned sector. China's economy is the largest in terms of purchasing power parity (PPP) and the second largest in terms of nominal GDP in the world.
Global revenue for the pharmaceutical sector reached $138.33 Bn in 2022, a significant increase over the preceding 20 years. Growth of the domestic pharmaceutical industries as several businesses are creating and producing generic cardiovascular medications that are both high-quality and reasonably priced, as China's domestic pharmaceutical market is expanding quickly. This increases market competition and lessens reliance on prescription imports.
Fosun Pharma is a multinational pharmaceutical and healthcare sector firm that engages directly in the areas of medical diagnostics, medicines, medical devices, and healthcare services. It broadens its operations in the retail and pharmaceutical distribution sectors. In the first half of 2023, the pharmaceutical industry brought in $2.26 Bn, growing 11.64% over the period-on-period growth.
Market Growth Drivers:
Adoption of Digital Healthcare Technologies: Increasing the use of online pharmacies and telemedicine is boosting patient convenience and improving access to cardiovascular drugs in rural places.
Government Initiatives: The Chinese government has put in place several programs to increase access to and the cost of healthcare, such as encouraging the use of generic medications. The market for necessary cardiovascular drugs is strengthened by this.
Growth of the Domestic Pharmaceutical Industry: As a result of the rapid expansion of China's domestic pharmaceutical market, numerous companies are developing and manufacturing generic cardiovascular drugs that are both of excellent quality and competitively priced.
Market Restraints Analysis:
Regulatory Obstacles: Pharmaceutical businesses operating in China may find it difficult to navigate the country's intricate regulatory environment. Strict approval procedures and frequent rule modifications might cause delays or prevent the release of new cardiovascular medications.
Pricing Pressures: The Chinese government's focus on affordability places a heavy weight on the cost of heart medications. This may discourage investment in novel and maybe more costly treatments by encouraging producers to concentrate on producing generic versions of their products.
Challenges related to Intellectual Property: Despite China's significant advancements in this area, issues with patent infringement and illicit generic production persist. This may deter international businesses from funding R&D for the Chinese market.
Under the State Council of China, the National Medical Products Administration (NMPA) is a national office overseeing drugs. It is run by the State Administration for Market Regulation. Applicant sends the NMPA a New Drug Application (NDA). The applicant's production facilities are inspected on-site by the NMPA once it has reviewed the NDA. The NMPA has the right to ask the applicant for more clinical data or other pertinent information. Regulations of the NMPA are often changed, necessitating ongoing attention and adjustment. The NMPA may have different criteria than other authorities.
Key Players:
1. Executive Summary
1.1 Disease Overview
1.2 Global Scenario
1.3 Country Overview
1.4 Healthcare Scenario in Country
1.5 Patient Journey
1.6 Health Insurance Coverage in Country
1.7 Active Pharmaceutical Ingredient (API)
1.8 Recent Developments in the Country
2. Market Size and Forecasting
2.1 Epidemiology of Disease
2.2 Market Size (With Excel & Methodology)
2.3 Market Segmentation (Check all Segments in Segmentation Section)
3. Market Dynamics
3.1 Market Drivers
3.2 Market Restraints
4. Competitive Landscape
4.1 Major Market Share
4.2 Key Company Profile (Check all Companies in the Summary Section)
4.2.1 Company
4.2.1.1 Overview
4.2.1.2 Product Applications and Services
4.2.1.3 Recent Developments
4.2.1.4 Partnerships Ecosystem
4.2.1.5 Financials (Based on Availability)
5. Reimbursement Scenario
5.1 Reimbursement Regulation
5.2 Reimbursement Process for Diagnosis
5.3 Reimbursement Process for Treatment
6. Methodology and Scope
By Drug Type
By Disease Indication
By Distribution Channel
Methodology for Database Creation
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