Prefilled Syringes Market Size - Growth, Trends, COVID-19 Impact, and Forecasts (2022 - 2027)

出版日期: | 出版商: Mordor Intelligence Pvt Ltd | 英文 114 Pages | 商品交期: 2-3個工作天內



  • 全貌
  • 簡介
  • 目錄




第1章 簡介

  • 市場定義

第2章 調查方法

第3章 摘要整理

第4章 主要影響要素

第5章 市場概要

  • 目前市場方案
  • 開發平台分析
  • 波特的五力分析
    • 供應商談判力
    • 消費者談判力
    • 新加入廠商的威脅
    • 替代產品與服務的威脅
    • 產業內的競爭
  • 法規方案

第6章 成長要素,阻礙因素,機會及挑戰分析(DROC)

  • 市場成長要素
    • 自我護理設備的普及
    • 預填充式注射器相關優點
    • 生技藥品預填充式注射器的使用增加
  • 市場阻礙因素
    • 產品回收
    • 替代藥物輸送方法的利用可能性
  • 市場機會
  • 主要課題

第7章 市場區隔

  • 各材料
    • 玻璃製預填充式注射器
    • 塑膠製預填充式注射器
  • 各應用領域
    • 糖尿病
    • 過敏性反應
    • 關節炎
    • 疫苗
    • 其他
  • 各類型
    • 拋棄式預填充式注射器
    • 可再使用的預填充式注射器
  • 各地區
    • 北美
    • 歐洲
    • 亞太地區
    • 中東、非洲
    • 南美

第8章 競爭情形

  • M&A分析
  • 協定,合作,夥伴關係
  • 新產品的銷售

第9章 主要企業

  • Becton, Dickinson and Company
  • Gerresheimer AG
  • Haselmeier AG
  • Medtronic
  • Nipro
  • Scandinavian Health Limited (SHL Group)
  • Stevanato Group
  • Terumo Corporation
  • Unilife Corporation

第10章 市場未來展望

Product Code: 61912

The market for prefilled syringes is projected to grow, owing to factors, such as increasing adoption of self-care devices, benefits associated with prefilled syringes, and high demand for improved safety in injectables.

The prefilled syringes make injections easy, accurate, and safe for, both, patients and doctors. Pre-filled syringes have emerged as one of the fastest-growing choices for unit dose medication, as the pharmaceutical industry seeks new and more convenient drug delivery methods.

In addition, pharmaceutical companies can get benefit by saving the cost of vials. The prefilled syringes work well with safety devices and auto-injection systems. Pharmaceutical companies are able to minimize drug waste and increase product life span, while patients are able to self-administer injectable drugs at their home instead of the hospital. Pre-filled syringes have also been utilized across a wide range of therapeutic sectors, such as vaccines, blood stimulants, and therapeutic proteins.

Eliminating dosing errors and ease of use are two of the greatest advantages of pre-filled syringes. Consequently, the differential advantages provided by prefilled syringes over traditional syringes are leading to the increased adoption and contributing to the global market growth.

Key Market Trends

Glass Prefilled Syringes are Projected to Experience Highest Growth Over the Forecast Period

The pharmaceutical industry uses glass syringes manufactured from Type 1 borosilicate glass, which consists primarily of silicon dioxide, along with oxides of boron, aluminum, sodium, and potassium. Metal ions, specifically sodium dioxide, are included in the mixture to alter the physical properties of the glass.

Glass syringes are manufactured from tubing glass. The glass tubing is created by heating the glass mixture to approximately 1500°C and continuously pulling the molten glass along a hollow spindle. Processing conditions, such as speed and airflow, are tightly controlled to prevent failures, such as airlines in the glass, from occurring. While glasses are generally unreactive, they are not necessarily inert. Alkali metals can leach out of glass, resulting in pH shifts in the solution. Some drug molecules are also labile for adsorption to the charged surface of the glass, resulting in decreased potency of the drug solution.

There have been reported instances when tungsten residues in the glass syringe Luer cone left behind during manufacturing have led to aggregation and particle formation in protein solutions. Apart from the above-mentioned challenges of drug interaction, glass prefilled syringes are also prone to breakage.

The market for glass prefilled syringes will grow regardless, albeit very sluggishly in the forecast period, primarily due to increased adoption of prefilled syringes in the developing regions, where glass syringes provide reusability and lower cost.

North America Dominates the Market

On January 22, 2013, the US FDA published the long-anticipated Final Rule: "Current Good Manufacturing Practice Requirements for Combination Products", with the purpose of clarifying regulatory requirements for quality systems used to design, develop, and manufacture combination products, and to help ensure consistent and appropriate application and enforcement of these requirements.

Prefilled drug delivery systems, including prefilled syringes, are combination products subject to the Final Rule. From a manufactures perspective, the Final Rule, as provided by the US FDA, tightens the regulations for syringe manufacturers and has made the manufacturing operation more stringent than before. This has acted as a deterrent to global players based in the United States and prevents them from expanding their regional operations, in other regions.

Overall, there is a large concentration of vendors supplying both end products and original components in the prefilled syringe market. The use of prefilled syringes in the United States is consequently ensured by the presence of appropriate vendors. Lifestyle associated illnesses and growing demand for easy-to-administer injectables in patients of chronic disease are helping the US prefilled syringe market flourish.

Competitive Landscape

The market for prefilled syringes is moderately competitive and there is high price competition in the market. The market is comprised of, both, global and local players. Most of the developing countries are having local players that provide prefilled syringes at a lower price. However, the market is majorly dominated by global companies. Few companies are expected to penetrate the market in the near future and they are expected to account for a substantial share of the prefilled syringes market.

Additional Benefits:

  • The market estimate (ME) sheet in Excel format
  • 3 months of analyst support



  • 1.1 Study Deliverables
  • 1.2 Study Assumptions
  • 1.3 Scope of the Study




  • 4.1 Market Overview
  • 4.2 Market Drivers
    • 4.2.1 Growing Adoption of Self-care Devices
    • 4.2.2 Benefits Associated with Prefilled Syringes
  • 4.3 Market Restraints
    • 4.3.1 Product Recalls
    • 4.3.2 Availability of Alternate Drug Delivery Methods
  • 4.4 Porter's Five Force Analysis
    • 4.4.1 Threat of New Entrants
    • 4.4.2 Bargaining Power of Buyers/Consumers
    • 4.4.3 Bargaining Power of Suppliers
    • 4.4.4 Threat of Substitute Products
    • 4.4.5 Intensity of Competitive Rivalry


  • 5.1 By Material
    • 5.1.1 Glass Prefilled Syringe
    • 5.1.2 Plastic Prefilled Syringe
  • 5.2 By Application
    • 5.2.1 Diabetes
    • 5.2.2 Anaphylaxis
    • 5.2.3 Rheumatoid Arthritis
    • 5.2.4 Oncology
    • 5.2.5 Other Applications
  • 5.3 By Type
    • 5.3.1 With Needle​
    • 5.3.2 Without Needle​
  • 5.4 Geography
    • 5.4.1 North America
      • United States
      • Canada
      • Mexico
    • 5.4.2 Europe
      • Germany
      • United Kingdom
      • France
      • Italy
      • Spain
      • Rest of Europe
    • 5.4.3 Asia-Pacific
      • China
      • Japan
      • India
      • Australia
      • South Korea
      • Rest of Asia-Pacific
    • 5.4.4 Middle-East and Africa
      • GCC
      • South Africa
      • Rest of Middle-East and Africa
    • 5.4.5 South America
      • Brazil
      • Argentina
      • Rest of South America


  • 6.1 Company Profiles
    • 6.1.1 Becton, Dickinson and Company
    • 6.1.2 B. Braun Melsungen AG​
    • 6.1.3 Johnson & Johnson​
    • 6.1.4 Baxter International Inc.
    • 6.1.5 Terumo Corporation​
    • 6.1.6 Pfizer Inc.​
    • 6.1.7 Cardinal Health Inc.​
    • 6.1.8 Teva Pharmaceuticals Industries Ltd​
    • 6.1.9 Fresenius SE & Co. KGaA​
    • 6.1.10 Mylan NV ​
    • 6.1.11 Sanofi SA​