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ORTHOPEDIC REGENERATIVE MEDICINE MARKET ANALYSIS

Orthopedic Regenerative Medicine Market, By Type (Stem Cell, Biomaterial and Tissue Engineering), By Application (Osteoarticular Diseases, Rheumatoid Arthritis, Ligament Injuries, Burisitis, Osteoporosis and Others), By Region (North America, Latin America, Europe, Asia Pacific, Middle East, and Africa)

  • Published In : Oct 2023
  • Code : CMI4841
  • Pages :180
  • Formats :
      Excel and PDF
  • Industry : Biotechnology

Market Challenges And Opportunities

  • Increasing product launch: Increasing product launches by key players in the market is expected to drive the growth of the global orthopedic regenerative medicine market. For instance, in March 2022, Molecular Matrix, Inc., a company that focuses on regenerative medicine polymer technology, announced the launch of its Osteo-P Synthetic Bone Graft Substitute (BGS) for use in the musculoskeletal system.
  • Increasing adoption of inorganic growth strategies such as partnership: Increasing adoption of inorganic growth strategies such as partnerships by the key players in the market is expected to drive the growth of the global orthopedic regenerative medicine market over the forecast period. For instance, in September 2020, DSM, a medical device company, announced a partnership with PBC Biomed, a medical device design and development company, to jointly design and develop novel materials for medical devices.

Global Orthopedic Regenerative Medicine Market: Restraint

  • Stringent government regulatory scenario in research and development of orthopedic regenerative medicine: Stringent government regulatory scenario in research and development of orthopedic regenerative medicine is expected to hamper the growth of the global orthopedic regenerative medicine market over the forecast period. Standards are rules, conditions, guidelines, or agreed-upon practices that are adopted within an industry to provide developers with a common framework and promote consistency. Developing regenerative medicine standards is challenging because these technologies and therapies are complex and rapidly evolving. Standards require consensus from stakeholders, which may be difficult to obtain. The U.S. Food and Drug Administration (FDA) ensures the safety, efficacy, and security of human medical products in the U.S. through regulation.

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