Drug Delivery Devices Market Scope And Analysis

  • Report Code : TIPHE100000854
  • Category : Life Sciences
  • Status : Published
  • No. of Pages : 289
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Drug Delivery Systems Market Analysis and Scope (2019 to 2027)

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Drug Delivery Systems Market Report Scope

Report Attribute Details
Market size in 2018 US$ 1,243.11 Billion
Market Size by 2027 US$ 2,302.23 Billion
Global CAGR (2018 - 2027) 7.2%
Historical Data 2016-2017
Forecast period 2019-2027
Segments Covered By Route of Administration
  • Oral
  • Transmucosal
  • Injectable
  • Topical
  • Implantable
  • Ocular
By Distribution Channel
  • Hospital Pharmacies
  • Retail Pharmacies
  • Online Pharmacies
By Application
  • Hospitals & Clinics
  • Home Care Settings
Regions and Countries Covered North America
  • US
  • Canada
  • Mexico
Europe
  • UK
  • Germany
  • France
  • Russia
  • Italy
  • Rest of Europe
Asia-Pacific
  • China
  • India
  • Japan
  • Australia
  • Rest of Asia-Pacific
South and Central America
  • Brazil
  • Argentina
  • Rest of South and Central America
Middle East and Africa
  • South Africa
  • Saudi Arabia
  • UAE
  • Rest of Middle East and Africa
Market leaders and key company profiles
  • BD Becton Dickinson Company
  • Boston Scientific Corporation
  • Novo Nordisk A S
  • Bausch Health Companies Inc
  • Baxter International Inc
  • Boehringer Ingelheim
  • Novartis AG
  • GlaxoSmithKline plc
  • Johnson Johnson Services Inc
  • Recent Developments:

     

    Inorganic and organic strategies such as mergers and acquisitions are highly adopted by companies in the drug delivery system market. A few recent key market developments are listed below: 

    • In June 2022, Gufic Biosciences Ltd launched a new drug delivery system, Dual Chamber Bags, at affordable prices for the first time in India. One of the most important USPs of these ready-to-use Dual Chamber Bags by Gufic is that they prevent contamination and protects the potency and efficacy of the drug. These bags also offer ease of handling at the time of reconstitution and also help in avoiding the dilution errors since the drug is present with the exact required quantity of the diluent to be used.
    • In February 2022, Takeda received US FDA approval for TAKHZYRO (lanadelumab-flyo) injection in a single-dose prefilled syringe (PFS), which is used to prevent attacks of hereditary angioedema (HAE) in adult and pediatric patients 12 years of age and older. The PFS is ready to use and requires fewer preparation steps than the current TAKHZYRO vial injection, while also reducing supplies and waste.