The GMP Cell Therapy Consumables Market is expected to grow
from US$ 11,031.25 million in 2021 to US$ 59,985.89 million by 2028; it is
estimated to grow at a CAGR of 27.5% from 2022 to 2028.

The “GMP
Cell Therapy Consumables Market” forecast 2028 report analyses the present
and future competitive scenario of the analytics industry. Gmp Cell Therapy
Consumables Market report offers an in-depth analysis on segments including top
companies, products, applications, revenue and regions. a number of topics
including likewise market share, drivers, trends and methods. This report
additionally offers insights into the latest growth and trends. It encapsulates
key aspects of the market, with focus on leading key player’s areas that have
witnessed the highest demand, leading regions and applications.

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The List of Companies -  

-         
Sartorius AG

-         
Thermo Fisher
Scientific Inc

-         
Miltenyi
Biotec BV & Co KG

-         
Bio-Techne
Corp

-         
Corning Inc

-         
FUJIFILM
Irvine Scientific Inc

-         
Lonza Group
AG

-         
BPS
Bioscience Inc

-         
Merck KGaA

-         
Global Life
Sciences Solutions USA LLC

Good
Manufacturing Practices (GMP) ensure that products are consistently produced
and controlled according to quality standards. Cell therapy manufacturing
processes are complex and require an underpinning pharmaceutical quality system
and quality control (QC) laboratory. Also, all aspects of cell therapy
manufacturing require trained personnel. As the process is complex, there may
be chances of contamination; therefore, GMP in cell therapy is becoming
mandatory. Also, the increasing use of cell therapy to treat various diseases
is propelling the demand for cell therapy consumables manufactured according to
GMP regulations.

The companies in the GMP cell therapy consumables market is
making strategic collaborations for the development of new products and cell
therapy treatments. A few strategic collaborations in the GMP cell therapy
consumables market is mentioned below:

- In October 2022, Pluristyx, panCELLa, and Implant
Therapeutics management announced the corporate merger, pending shareholder
approval. The merged company will combine complementary portfolios to offer
end-to-end customer support and provide increased access to a wide range of
induced pluripotent stem cell (iPSC)-related products and services. The
integrated technology and service offerings will greatly accelerate the
development and delivery of revolutionary cell therapies to patients.

- In November 2021, Laurus Labs signed an investment
agreement with Immunoadoptive Cell Therapy Private Limited (ImmunoACT), an
advanced cell and gene therapy company, to acquire a 26.62% stake (fully
diluted basis), subject to the fulfillment of certain conditions.

The increase in strategic collaborations among market
players for cell therapy development has propelled the use of GMP cell therapy
consumables to achieve the desired products, which drives the growth of the GMP
cell therapy consumables market.

Based on process, the GMP cell therapy consumables market is
segmented into cell collection and characterization/sorting and separation,
cell culture and expansion/preparation, cryopreservation, cell processing and
formulation, cell isolation and activation, cell distribution/handling, process
monitoring and control/readministration/quality assurance, and others.. The
cell collection and characterization/sorting and separation segment held the
largest market share in 2021. However, the cryopreservation segment is expected
to register the highest CAGR during the forecast period.

Cryopreservation has become a significant aspect of the
manufacturing process for many cellular therapies. It occasionally comes before
cell culture (conserving the starting cellular material before moving forward
with large-scale manufacturing) and generally follows cell expansion therapies.
The ability to store cells at different points during the manufacturing process
enables the creation of a customized workflow. Selecting GMP-grade or suitable
cryoprotective agents (CPAs) and controlled-rate freezing equipment with
appropriate cooling profiles for immune cells is one of the best practices
adopted to help generate high-quality cells. Sartorius designs NutriFreez cell
freezing solutions for the cryopreservation of cells manufactured in compliance
with GMP services.

In the US, leukemia treatment using CAR T-cell therapy costs
around US$ 800,000 to US$ 900,000. However, Indian start-ups and pharmaceutical
companies are focusing on offering this treatment at a lower cost by reducing
the treatment time and increasing the effectiveness of cell therapy. Also, the
government is investing in cell therapy for leukemia treatment. For instance,
in June 2021, the Department of Biotechnology (DBT) supported the first CAR
T-cell therapy conducted at ACTREC, Tata Memorial Center in Mumbai. This
increased the demand for cell therapy consumables in India as Phase I/II trials
were carried out in the country.

The World Health Organization (WHO), US Food and Drug
Administration (FDA), US Centers for Medicare & Medicaid Services, and Johns
Hopkins University are among the primary and secondary sources referred to
while preparing the report on the GMP cell therapy consumables market.

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TABLE OF CONTENTS

1. Introduction

   1.1 Study Scope

   1.2 The Insight Partners Research Report
Guidance

  
1.3 Market Segmentation

         1.3.1 by Product

         1.3.2 by Cell Therapy

         1.3.3 by End Use

         1.3.4 by End Use

         1.3.5 by Geography

2. Key Takeaways

3. Research Methodology

   3.1 Coverage

   3.2 Secondary Research

   3.3 Primary Research

4. Market Landscape

   4.1 Overview

   4.2 PEST Analysis

         4.2.1 North America PEST Analysis

         4.2.2 Europe PEST Analysis

         4.2.3 Asia Pacific PEST Analysis

         4.2.4 South & Central America PEST
Analysis

         4.2.5 Middle East & Africa PEST
Analysis

   4.3 Experts' Opinion

5. Key Market Dynamics

   5.1 Market Drivers

         5.1.1 Rise in Research & Development
and Drug Discovery

         5.1.2 Increase in Strategic
Collaborations

   5.2 Market Restraints

         5.2.1 Stringent Regulatory Policies

   5.3 Market Opportunities

         5.3.1 Growing Regulatory Approvals for
Cell and Gene Therapy (CGT) Product

   5.4 Future Trends

         5.4.1 Increasing Clinical Trials and
Rising GMP Demand

   5.5 Impact Analysis

6. Global Analysis

7. Revenue and Forecast to 2028 -
by Product

Continued…

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