Brazil's biosimilars market size was valued at $0.4 Bn in 2022 and is estimated to expand at a compound annual growth rate (CAGR) of 23.2% from 2022 to 2030 and will reach $2.5 Bn in 2030. The market is segmented by product type and indication type. The Brazil Biosimilars market will grow with The increased incidence of chronic illnesses, rising healthcare expenses, and the demand for affordable biologic medicine substitutes. The key market players are Roche (CHE), Novartis (CHE), Pfizer (USA), Sanofi (FRA), Merck (USA), and others.
The Brazil Biosimilars market size was valued at $0.4 Bn in 2022 and is estimated to expand at a compound annual growth rate (CAGR) of 23.2% from 2022 to 2030 and will reach $2.5 Bn in 2030. Brazil is the ninth-largest economy in the world, and it boasts one of the biggest and most complicated healthcare systems in the region. The service industry makes up the majority of Brazil's economy, contributing to over 70% of its GDP. Public and commercial healthcare services are both provided under Brazil's mixed healthcare system. Brazilian people can receive free medical treatment through the public healthcare system, known as the Brazilian Unified Health System (SUS), while those who can afford to pay for it can receive care from the private healthcare industry. With a population of over 200 million, the SUS is the world's biggest public healthcare system.
Biosimilars are biological medications that, although not exact replicas of the reference biologics are quite similar to them. Brazil has seen steady growth in the usage of biosimilars over the years as the nation works to improve patient access to low-cost, high-quality medical care. The biosimilar market in Brazil presents significant opportunities for both multinational and local manufacturers, as the country seeks to expand access to affordable and effective treatments for patients.
Market Growth Drivers
In Brazil, several of the original biologic medications that are used to treat illnesses are losing their patent protection, allowing biosimilars to reach the market. Additionally. Because biosimilars are often more affordable than reference biologics, individuals and healthcare systems can save a lot of money by using them. Biosimilars can expand patient access to necessary therapies by lowering costs and increasing availability. The Brazilian government has taken a number of steps to encourage the use of biosimilars, including urging doctors to prescribe them instead of reference biologics and fostering the growth of a biosimilar sector there.
Market Restraints
Brazilian doctors and patients might not be familiar with biosimilars or could worry about their efficacy and safety. Brazil's licensing procedure for biosimilars can be intricate and drawn out, delaying their arrival onto the market.
Furthermore, doctors and patients could have a strong preference for reference biologics, which makes it challenging for biosimilars to obtain market dominance.
Key Players
The National Health Surveillance Agency (ANVISA) in Brazil is the regulatory body in charge of authorizing biosimilars. The stringent approval procedure for biosimilars calls for extensive preclinical and clinical research.
Similar to reference biologics, biosimilars are paid in Brazil through the Brazilian Public Health System (SUS). The same pricing and reimbursement rules that apply to reference biologics also apply to biosimilars. These rules include a reference price system and prices that producers and the Brazilian government have agreed upon. The Brazilian Biosimilar Policy, which intends to encourage the use of biosimilars in the Brazilian healthcare system, also includes biosimilars.
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 Product
The monoclonal antibodies, insulin, granulocyte colony-stimulating factor, erythropoietin, recombinant human growth hormone, etanercept, follitropin, teriparatide, interferons, enoxaparin sodium, glucagon, and calcitonin are among the product categories that make up the biosimilars market. Monoclonal antibodies held a sizable portion of the market in 2020. The market is being driven by elements including the widespread use of monoclonal antibodies in the treatment of autoimmune diseases, cancer, and osteoporosis, as well as the affordability of such treatments.
By Indication
The biosimilars market is divided into oncology, autoimmune and inflammatory diseases, chronic illnesses, blood disorders, growth hormone insufficiency, infectious diseases, and other indications based on the indication (infertility, hypoglycemia, myocardial infarction, postmenopausal osteoporosis, chronic kidney failure, and ophthalmic diseases). The market's largest sector in 2020 will be oncology. This market is expanding as a result of elements like the reduced cost of biosimilars compared to novel biologics and the increased incidence and prevalence of cancer.
Methodology for Database Creation
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How Do We Get It?
Our database is created and maintained through a combination of secondary and primary research methodologies.
1. Secondary Research
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2. Primary Research
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Combining Secondary and Primary Research
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