Pharmaceutical Stability and Storage Services Market Size to Surpass USD 5.24 Bn by 2032

The global pharmaceutical stability and storage services market size reached USD 3.21 billion in 2023 and is projected to surpass around USD 5.24 billion by 2032, with a CAGR of 5.6% from 2023 to 2032.

Ottawa, Feb. 12, 2024 (GLOBE NEWSWIRE) — The pharmaceutical stability and storage services market size accounted for USD 3.38 billion in 2024 and is estimated to reach around USD 4.42 billion by 2029, According to Precedence Research. North America led the market with the largest market share of 54% in 2022.

The pharmaceutical stability and storage services market is driven by the growing pharmaceutical sector, the rise in personalized medicine, technological advancements, rising outsourcing trends and others.

The U.S. pharmaceutical stability and storage services market size was USD 1.49 billion in 2023, grew to USD 1.57 billion in 2024, and is expected to surpass around USD 2.49 billion by 2032, growing at a CAGR of 5.6% from 2023 to 2032.

Pharmaceutical stability and storage services are critical aspects of the pharmaceutical industry that focus on maintaining the quality, safety and efficacy of pharmaceutical products throughout their lifecycle. These services ensure that drugs and other medical products remain stable, potent, and safe for use from the time of manufacturing through distribution, storage and until they reach the end-user. The growing investment is expected to drive the pharmaceutical stability and storage services industry during the forecast period.

  • For instance, after investing more than USD 1.25 million, the Advanced Therapeutic Medicinal Products (ATMP) and small molecule diagnostics provider, Symbiosis Pharmaceutical Services, a specialized Contract Development and Manufacturing Organization (CDMO), has introduced new internal analytical and microbiological capabilities. Completely approved by the UK Regulatory Agency (MHRA), this service offering expansion will strategically improve the business’s primary sterile manufacturing service (also known as “fill/finish”) and offer a comprehensive internal Quality Control (QC) function to support Symbiosis’s aseptic product manufacturing.

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Key Insights:

  • The stability segment is expected to dominate the market during the forecast period.
  • The small molecule segment is expected to capture a significant market share over the forecast period.
  • The in-house segment held the largest market share in 2023 of more than 60% and is expected to continue the same pattern during the forecast period.

Global Pharmaceutical Stability and Storage Services Market, By Region, 2022-2032 (USD Million)

Region 2022 2023 2027 2032
North America 1,649.10 1,735.50 2,148.90 2,867.30
Europe 616.3 650.4 813.9 1,100.20
Asia Pacific 597.3 629.3 782.8 1,050.30
LAMEA 192.8 196.2 210 226
  • North America is expected to hold a significant market share during the forecast period. The market growth in the region is attributed to the growing biopharmaceutical sector. The biopharmaceutical sector in North America is significant, with a high number of biotech and pharmaceutical companies developing and manufacturing biologics. These products often have specific storage requirements, driving the demand for specialized stability and storage services.
  • For instance, according to recently disclosed statistics on the US bioscience sector, the Biotechnology Innovation Organization (BIO) and the Council of State Bioscience Associations (CSBA) estimated its value at USD 2.9 trillion in 2021. According to the research, nearly 127,000 enterprises in the US industry employed 2.1 million people in 2021.
  • Over the anticipated period, the need for pharmaceutical stability and storage services will also be driven by the rising prevalence of uncommon disorders and specialized medications. A sickness or condition that affects fewer than 200,000 Americans is considered a rare disorder, according to the National Organization for Rare Disorders, Inc. Overall, about 30 million Americans suffer from more than 7,000 rare diseases. Thus, the aforementioned statistics are expected to propel the market expansion during the forecast period.

The North America pharmaceutical stability and storage services market size was reached at USD 1.73 billion in 2023 and is anticipated to reach around USD 2.86 billion by 2032.

The Europe pharmaceutical stability and storage services market size was valued at USD 650.4 million in 2023 and is projected to hit around USD 1,100.2 million by 2032.

The Asia Pacific pharmaceutical stability and storage services market size surpassed USD 597.3 million in 2023 and is expected to be worth around USD 1,050.3 million by 2032.

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Pharmaceutical Stability and Storage Services Market Scope

Report Coverage Details
Global Market Size in 2023 USD 3.21 Billion
Global Market Size by 2032 USD 5.24 Billion
Growth Rate from 2023 to 2032 CAGR of 5.6%
U.S. Market Size in 2023 USD 1.49 Billion
U.S. Market Size by 2032 USD 2.49 Billion
Base Year 2022
Forecast Period 2023 to 2032
Segments Covered By Services, By Molecule, By Mode, and Geography

Pharmaceutical Stability and Storage Services Market Report Highlights:

Global Pharmaceutical Stability and Storage Services Market, By Services, 2022-2032 (USD Million)

Services 2022 2023 2027 2032
Stability 1,976.60 2,080.10 2,575.10 3,435.10
Storage 1,078.90 1,131.30 1,380.60 1,808.80

The stability segment is expected to dominate the market during the forecast period. Stability testing involves subjecting pharmaceutical products to specific environmental conditions such as temperature, humidity and light over a designated period.

The aim is to assess the product quality properties variations over time. These tests are also provided by specialized facilities to pharmaceutical companies. These facilities create controlled environments and conduct studies to determine the shelf life, storage conditions, and packaging requirements for different drug formulations. Thereby, driving the segment expansion.

Global Pharmaceutical Stability and Storage Services Market, By Molecules, 2022-2032 (USD Million)

Molecules 2022 2023 2027 2032
Small Molecule 1,676.50 1,763.90 2,182.30 2,908.70
Large Molecule 1,379.00 1,447.40 1,773.40 2,335.10

The small molecule segment is expected to capture a significant market share over the forecast period. Continuous monitoring of storage conditions is essential for small molecule drugs. Real-time monitoring systems are employed to ensure that temperature, humidity and other environmental factors remain within specific limits. Additionally, the development of small molecule drugs has come a long way in the past thirty years. Approximately 90% of all pharmaceutical medications are small molecules. Fever, migraines, cancer, diabetes, and other prevalent diseases are all treated with it. The need for safe testing and storage of small-molecule pharmaceuticals is being driven by their application in the treatment of prevalent diseases and conditions.

Global Pharmaceutical Stability and Storage Services Market, By Modes, 2022-2032 (USD Million)

Modes 2022 2023 2027 2032
In-house 1,816.80 1,911.90 2,366.90 3,157.20
Outsourcing 1,238.70 1,299.40 1,588.80 2,086.70

The in-house segment held the largest market share in 2023 of more than 60% and is expected to continue the same pattern during the forecast period. The segment expansion is attributed to the advantages of in-house stability services. These services provide companies with direct control and oversight of stability testing processes and conditions. In addition, companies can make real-time decisions regarding product stability, allowing for swift adjustments to formulations, packaging or storage conditions.

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Market Dynamics:

Driver: Increasing demand for biosimilars

The market for biosimilars has grown dramatically in recent years because of their similarity to biologics and generally cheaper cost. The use of biosimilars in the treatment of autoimmune disorders, cancer, and other chronic illnesses has grown significantly. Due to the high frequency of these diseases around the world, there will likely be an increase in demand for biosimilars as well as a need for their stability and storage. Because different regulatory bodies have varying data requirements and testing criteria for evaluating a product’s stability, marketing items throughout the market can be difficult. This is expected to raise the need for outsourcing services in the industry.        

Restraint: High investment and complex regulatory landscape

Establishing and maintaining state-of-the-art stability and storage facilities require significant capital investment. This can be a restraint, especially for smaller pharmaceutical companies with limited financial resources. In addition, compliance with stringent regulatory requirements, including Good Manufacturing Practices (GMP) and other guidelines, can be challenging and resource intensive. Meeting regulatory standards for storage and stability testing necessitates ongoing investments in technology, personnel, and infrastructure. Therefore, the high investment and complex regulatory landscape might be a major restraining factor for the market expansion.

Opportunity: Growing complexity of pharmaceuticals

The pharmaceutical industry is evolving with the development of more complex and sensitive drug formulations. Specialized storage and stability services are required to meet the unique needs of these products, which may be susceptible to temperature fluctuations, light exposure, or other environmental factors. Thus, these complexities in the pharmaceutical industry are expected to offer a lucrative opportunity for the pharmaceutical stability and storage services market during the forecast period.

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Recent Developments:

  • In October 2022, Cambrex announced the growth of Q1 Scientific, its stability storage division that provides pharmaceutical, medical device, and life sciences businesses with environmentally controlled stability storage services. Q1 Scientific plans to expand its Waterford, Ireland, location by 10,000 square feet and construct a new 20,000-square-foot cGMP facility in Belgium. Situated around 50 miles from Brussels in the conveniently accessible Liege region, Q1 Scientific’s new state-of-the-art temperature-controlled and monitored storage facility will be built in Belgium. To facilitate long-term, intermediate, and expedited stability studies, the facility will offer 35,000 temperature-controlled storage rooms for all major ICH climatic zones, including 2–8°C and 25°C / 60%RH and 40°C / 75%RH.
  • In October 2023, the range of high-performing pharmaceutical component solutions from Clariant, a specialty chemicals firm with a focus on sustainability, has been expanded to include new products that will aid in the development of safe and efficient medications. To position itself as the industry’s one-stop shop for solutions, Clariant will introduce three new VitiPure® excipients at CPHI Barcelona. These excipients enable a variety of Active Pharmaceutical Ingredient (API) formulations and administration routes, even for sensitive ones like mRNA vaccines and biological medications.

Market Key Players:

  • Catalent, Inc.
  • Charles River Laboratories International, Inc
  • Almac Group
  • Eurofins Scientific
  • Lucideon Limited
  • Intertek Group Plc
  • Alcami Corporation
  • Element Materials Technology
  • Q1 Scientific
  • BioLife Solutions
  • Masy BioServices
  • Roylance Stability Storage Limited
  • Reading Scientific Services Ltd.
  • Als Ltd.
  • Auriga Research Private Limited

Market Segmentation

By Services

  • Stability
    • Drug Substance
    • Stability Indicating Method Validation
    • Accelerated Stability Testing
    • Photostability Testing
    • Others
  • Storage
    • Cold
    • Non-cold

By Molecule

  • Small Molecule
    • Research Products
    • Commercial Products
  • Large Molecule
    • Research Products
    • Commercial Products

By Mode

  • In-house
  • Outsourcing

By Geography

  • North America
  • Europe
  • Asia-Pacific
  • Latin America
  • The Middle East and Africa

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