Please Wait.....
Report
Lysosomal Storage Diseases Therapeutics Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, Segmented By Treatment (Enzyme Replacement Therapy, Stem Cell Therapy, Substrate Reduction Therapy, others), By Indication (Gaucher's Disease, Fabry Disease, Pompe's Disease, Mucopolysaccharidosis, others), By End User (Hospitals, Clinics), By Region & Competition, 2020-2030F
Market Report I 2025-03-24 I 180 Pages I TechSci Research
Global Lysosomal Storage Diseases Therapeutics Market was valued at USD 7.60 billion in 2024 and is anticipated to witness an impressive growth in the forecast period with a CAGR of 7.20% through 2030. Lysosomal Storage Diseases (LSDs), also known as lysosomal storage disorders, are a group of rare genetic disorders characterized by abnormalities in lysosomes. Lysosomes are cellular organelles responsible for breaking down various molecules and cellular waste products. When lysosomes malfunction due to genetic mutations, they cannot perform their normal functions effectively. As a result, undigested substances accumulate within the lysosomes and disrupt cellular processes. This accumulation leads to a wide range of symptoms and organ damage, affecting multiple systems in the body. Most LSDs result from deficiencies of specific lysosomal enzymes. These enzymes are responsible for breaking down complex molecules, such as lipids (fats), glycoproteins, and mucopolysaccharides. When a particular enzyme is deficient or absent, the corresponding substrate accumulates within lysosomes. There are over 50 different LSDs, each associated with a specific lysosomal enzyme deficiency. Examples of LSDs include Gaucher's disease, Tay-Sachs disease, Fabry disease, Pompe disease, Niemann-Pick disease, and mucopolysaccharidoses (MPS). Each LSD has its unique clinical features and disease course. For instance, according to the National Institutes of Health (NIH), as of April 2022, Pompe disease affects approximately 1 in 40,000 individuals in the United States.
Key Market Drivers
Advances in Research and Development
Gene therapy has emerged as a promising approach for treating certain LSDs. Researchers are exploring methods to deliver functional genes into affected cells to restore enzyme production. Clinical trials and studies have shown promising results for diseases like mucopolysaccharidosis type II (Hunter syndrome) and Niemann-Pick disease type A and B. According to a July 2022 study published by the National Library of Medicine, lysosomal storage disorders (LSDs) are more prevalent when considered collectively, with a combined incidence of 1 in 5,000 to 1 in 8,000. The study highlights that ethnicity and geography influence LSD occurrence. For instance, Gaucher disease (GD) affects 1 in 40,000 to 1 in 60,000 in the general population but is significantly higher among Ashkenazi Jews (1 in 800). Similarly, Tay-Sachs disease (1 in 3,900), Niemann-Pick A, and mucolipidosis IV are more common in this group. In Finland, aspartylglucosaminuria occurs in 1 in 18,500 individuals. The increasing burden of LSDs is expected to drive market growth for lysosomal storage disease treatments in the coming years.
Small molecule chaperones are designed to stabilize mutant enzymes, allowing them to function more effectively. These therapies aim to correct the underlying enzymatic defects in LSDs. Some chaperone therapies have received regulatory approval and are available for patients with conditions like Fabry disease. Substrate Reduction Therapy (SRT) involves reducing the production of the toxic substrate that accumulates in lysosomes in LSDs. Medications like miglustat and eliglustat have been developed as SRTs and are used to treat diseases such as Gaucher's disease and Niemann-Pick type C. Ongoing research has led to the development of improved Enzyme Replacement Therapy (ERTs) with enhanced stability, bioavailability, and pharmacokinetics. These advancements aim to increase the effectiveness and convenience of treatment for patients with LSDs. Researchers are investigating the potential benefits of combining different therapeutic approaches, such as ERTs with chaperone therapies or gene therapy with small molecules. These combinations may offer synergistic effects and improved patient outcomes. Advances in biomarker research have led to the identification of specific markers that can aid in the diagnosis, monitoring, and assessment of disease progression in LSDs.
Key Market Challenges
Limited Understanding of Disease Mechanisms
In many LSDs, the underlying genetic and molecular mechanisms are complex and not fully understood. This complexity makes it challenging to develop targeted therapies that address the root cause of the disease. Without a comprehensive understanding of the disease mechanisms, it is difficult to identify specific drug targets and design effective treatments. LSDs encompass a wide range of rare genetic disorders, each with its unique pathophysiology. Understanding the variations in disease mechanisms among different LSDs is essential for developing tailored treatments. Limited knowledge of these variations can hinder therapeutic development efforts. Biomarkers are crucial for disease diagnosis, monitoring, and assessing treatment efficacy. However, without a deep understanding of disease mechanisms, it can be challenging to identify reliable biomarkers for LSDs, which are necessary for clinical trials and personalized medicine approaches. The lack of insight into disease mechanisms contributes to a high failure rate in drug development for LSDs. Many potential drug candidates do not progress past preclinical or early clinical stages because they do not effectively target the underlying disease processes. In the absence of a clear understanding of disease mechanisms, drug developers may face challenges related to off-target effects. These unintended consequences can lead to safety concerns and hinder the development of safe and effective therapies. The complexity of LSDs and the limited understanding of their mechanisms can make it difficult to secure research funding. Potential investors and grant providers may be hesitant to fund projects without a clear path to success, leading to underfunding of critical research efforts.
Key Market Trends
Chaperone Therapies
Chaperone therapies involve the use of small molecules that can stabilize and enhance the activity of misfolded or unstable lysosomal enzymes in LSDs. These molecules act as chaperones by assisting in the correct folding and trafficking of the enzyme to its target location within the lysosome. Chaperone therapies are designed to address the specific genetic mutations that lead to enzyme misfolding and dysfunction in LSDs. They target the underlying cause of the disease by helping the enzyme reach its active form, which is essential for substrate degradation. Many chaperone therapies are administered orally, which is a more convenient and patient-friendly route of administration compared to intravenous infusions or other invasive methods. This can improve treatment adherence and patient quality of life. Chaperone therapies have been developed and tested for various LSDs, including Fabry disease, Pompe disease, Gaucher's disease, and others. This broad applicability makes them relevant to multiple LSD subtypes. Some chaperone therapies have demonstrated clinical success and received regulatory approvals in different regions. For example, migalastat has been approved for the treatment of Fabry disease. Chaperone therapies hold the potential to modify the course of the disease by restoring enzyme activity and reducing substrate accumulation. This can lead to improvements in clinical outcomes and the prevention of disease progression. Researchers are exploring the possibility of combining chaperone therapies with other treatment approaches, such as enzyme replacement therapy (ERT) or gene therapy. These combination therapies may offer synergistic benefits and enhanced treatment efficacy. Chaperone therapies align with the trend toward personalized and precision medicine, where treatments are tailored to individual patients based on their specific genetic mutations and disease manifestations.
Key Market Players
- Pfizer, Inc.
- Sanofi SA
- BioMarin Pharmaceutical Inc
- Actelion Ltd.
- Raptor Pharmaceutical Corp.
- Protalix Biotherapeutics Inc.
- Amicus Therapeutics, Inc.
- Quest Diagnostics Inc.
- Amicus Therapeutics Inc.
- Shire Plc
Report Scope:
In this report, the Global Lysosomal Storage Diseases Therapeutics Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:
- Lysosomal Storage Diseases Therapeutics Market, By Treatment:
o Enzyme Replacement Therapy
o Stem Cell Therapy
o Substrate Reduction Therapy
o Others
- Lysosomal Storage Diseases Therapeutics Market, By Indication:
o Gaucher's Disease
o Fabry Disease
o Pompe's Syndrome
o Mucopolysaccharidosis
o Others
- Lysosomal Storage Diseases Therapeutics Market, By End-User:
o Hospitals
o Clinics
- Lysosomal Storage Diseases Therapeutics Market, By region:
o North America
United States
Canada
Mexico
o Asia-Pacific
China
India
South Korea
Australia
Japan
o Europe
Germany
France
United Kingdom
Spain
Italy
o South America
Brazil
Argentina
Colombia
o Middle East & Africa
South Africa
Saudi Arabia
UAE
Competitive Landscape
Company Profiles: Detailed analysis of the major companies present in the Global Lysosomal Storage Diseases Therapeutics Market.
Available Customizations:
Global Lysosomal Storage Diseases Therapeutics Market report with the given market data, TechSci Research offers customizations according to a company's specific needs. The following customization options are available for the report:
Company Information
- Detailed analysis and profiling of additional market players (up to five).
1. Product Overview
1.1. Market Definition
1.2. Scope of the Market
1.2.1. Markets Covered
1.2.2. Years Considered for Study
1.2.3. Key Market Segmentations
2. Research Methodology
2.1. Objective of the Study
2.2. Baseline Methodology
2.3. Key Industry Partners
2.4. Major Association and Secondary Sources
2.5. Forecasting Methodology
2.6. Data Triangulation & Validation
2.7. Assumptions and Limitations
3. Executive Summary
3.1. Overview of the Market
3.2. Overview of Key Market Segmentations
3.3. Overview of Key Market Players
3.4. Overview of Key Regions/Countries
3.5. Overview of Market Drivers, Challenges, Trends
4. Voice of Customer
5. Global Lysosomal Storage Diseases Therapeutics Market Outlook
5.1. Market Size & Forecast
5.1.1. By Value
5.2. Market Share & Forecast
5.2.1. By Treatment (Enzyme Replacement Therapy, Stem Cell Therapy, Substrate Reduction Therapy, others)
5.2.2. By Indication (Gaucher's Disease, Fabry Disease, Pompe's Disease, Mucopolysaccharidosis, others)
5.2.3. By End User (Hospitals, Clinics),
5.2.4. By Region
5.2.5. By Company (2024)
5.3. Market Map
6. Asia Pacific Lysosomal Storage Diseases Therapeutics Market Outlook
6.1. Market Size & Forecast
6.1.1. By Value
6.2. Market Share & Forecast
6.2.1. By Treatment
6.2.2. By Indication
6.2.3. By End User
6.2.4. By Country
6.3. Asia Pacific: Country Analysis
6.3.1. China Lysosomal Storage Diseases Therapeutics Market Outlook
6.3.1.1. Market Size & Forecast
6.3.1.1.1. By Value
6.3.1.2. Market Share & Forecast
6.3.1.2.1. By Treatment
6.3.1.2.2. By Indication
6.3.1.2.3. By End User
6.3.2. India Lysosomal Storage Diseases Therapeutics Market Outlook
6.3.2.1. Market Size & Forecast
6.3.2.1.1. By Value
6.3.2.2. Market Share & Forecast
6.3.2.2.1. By Treatment
6.3.2.2.2. By Indication
6.3.2.2.3. By End User
6.3.3. Australia Lysosomal Storage Diseases Therapeutics Market Outlook
6.3.3.1. Market Size & Forecast
6.3.3.1.1. By Value
6.3.3.2. Market Share & Forecast
6.3.3.2.1. By Treatment
6.3.3.2.2. By Indication
6.3.3.2.3. By End User
6.3.4. Japan Lysosomal Storage Diseases Therapeutics Market Outlook
6.3.4.1. Market Size & Forecast
6.3.4.1.1. By Value
6.3.4.2. Market Share & Forecast
6.3.4.2.1. By Treatment
6.3.4.2.2. By Indication
6.3.4.2.3. By End User
6.3.5. South Korea Lysosomal Storage Diseases Therapeutics Market Outlook
6.3.5.1. Market Size & Forecast
6.3.5.1.1. By Value
6.3.5.2. Market Share & Forecast
6.3.5.2.1. By Treatment
6.3.5.2.2. By Indication
6.3.5.2.3. By End User
7. Europe Lysosomal Storage Diseases Therapeutics Market Outlook
7.1. Market Size & Forecast
7.1.1. By Value
7.2. Market Share & Forecast
7.2.1. By Treatment
7.2.2. By Indication
7.2.3. By End User
7.2.4. By Country
7.3. Europe: Country Analysis
7.3.1. France Lysosomal Storage Diseases Therapeutics Market Outlook
7.3.1.1. Market Size & Forecast
7.3.1.1.1. By Value
7.3.1.2. Market Share & Forecast
7.3.1.2.1. By Treatment
7.3.1.2.2. By Indication
7.3.1.2.3. By End User
7.3.2. Germany Lysosomal Storage Diseases Therapeutics Market Outlook
7.3.2.1. Market Size & Forecast
7.3.2.1.1. By Value
7.3.2.2. Market Share & Forecast
7.3.2.2.1. By Treatment
7.3.2.2.2. By Indication
7.3.2.2.3. By End User
7.3.3. Spain Lysosomal Storage Diseases Therapeutics Market Outlook
7.3.3.1. Market Size & Forecast
7.3.3.1.1. By Value
7.3.3.2. Market Share & Forecast
7.3.3.2.1. By Treatment
7.3.3.2.2. By Indication
7.3.3.2.3. By End User
7.3.4. Italy Lysosomal Storage Diseases Therapeutics Market Outlook
7.3.4.1. Market Size & Forecast
7.3.4.1.1. By Value
7.3.4.2. Market Share & Forecast
7.3.4.2.1. By Treatment
7.3.4.2.2. By Indication
7.3.4.2.3. By End User
7.3.5. United Kingdom Lysosomal Storage Diseases Therapeutics Market Outlook
7.3.5.1. Market Size & Forecast
7.3.5.1.1. By Value
7.3.5.2. Market Share & Forecast
7.3.5.2.1. By Treatment
7.3.5.2.2. By Indication
7.3.5.2.3. By End User
8. North America Lysosomal Storage Diseases Therapeutics Market Outlook
8.1. Market Size & Forecast
8.1.1. By Value
8.2. Market Share & Forecast
8.2.1. By Treatment
8.2.2. By Indication
8.2.3. By End User
8.2.4. By Country
8.3. North America: Country Analysis
8.3.1. United States Lysosomal Storage Diseases Therapeutics Market Outlook
8.3.1.1. Market Size & Forecast
8.3.1.1.1. By Value
8.3.1.2. Market Share & Forecast
8.3.1.2.1. By Treatment
8.3.1.2.2. By Indication
8.3.1.2.3. By End User
8.3.2. Mexico Lysosomal Storage Diseases Therapeutics Market Outlook
8.3.2.1. Market Size & Forecast
8.3.2.1.1. By Value
8.3.2.2. Market Share & Forecast
8.3.2.2.1. By Treatment
8.3.2.2.2. By Indication
8.3.2.2.3. By End User
8.3.3. Canada Lysosomal Storage Diseases Therapeutics Market Outlook
8.3.3.1. Market Size & Forecast
8.3.3.1.1. By Value
8.3.3.2. Market Share & Forecast
8.3.3.2.1. By Treatment
8.3.3.2.2. By Indication
8.3.3.2.3. By End User
9. South America Lysosomal Storage Diseases Therapeutics Market Outlook
9.1. Market Size & Forecast
9.1.1. By Value
9.2. Market Share & Forecast
9.2.1. By Treatment
9.2.2. By Indication
9.2.3. By End User
9.2.4. By Country
9.3. South America: Country Analysis
9.3.1. Brazil Lysosomal Storage Diseases Therapeutics Market Outlook
9.3.1.1. Market Size & Forecast
9.3.1.1.1. By Value
9.3.1.2. Market Share & Forecast
9.3.1.2.1. By Treatment
9.3.1.2.2. By Indication
9.3.1.2.3. By End User
9.3.2. Argentina Lysosomal Storage Diseases Therapeutics Market Outlook
9.3.2.1. Market Size & Forecast
9.3.2.1.1. By Value
9.3.2.2. Market Share & Forecast
9.3.2.2.1. By Treatment
9.3.2.2.2. By Indication
9.3.2.2.3. By End User
9.3.3. Colombia Lysosomal Storage Diseases Therapeutics Market Outlook
9.3.3.1. Market Size & Forecast
9.3.3.1.1. By Value
9.3.3.2. Market Share & Forecast
9.3.3.2.1. By Treatment
9.3.3.2.2. By Indication
9.3.3.2.3. By End User
10. Middle East and Africa Lysosomal Storage Diseases Therapeutics Market Outlook
10.1. Market Size & Forecast
10.1.1. By Value
10.2. Market Share & Forecast
10.2.1. By Treatment
10.2.2. By Indication
10.2.3. By End User
10.2.4. By Country
10.3. MEA: Country Analysis
10.3.1. South Africa Lysosomal Storage Diseases Therapeutics Market Outlook
10.3.1.1. Market Size & Forecast
10.3.1.1.1. By Value
10.3.1.2. Market Share & Forecast
10.3.1.2.1. By Treatment
10.3.1.2.2. By Indication
10.3.1.2.3. By End User
10.3.2. Saudi Arabia Lysosomal Storage Diseases Therapeutics Market Outlook
10.3.2.1. Market Size & Forecast
10.3.2.1.1. By Value
10.3.2.2. Market Share & Forecast
10.3.2.2.1. By Treatment
10.3.2.2.2. By Indication
10.3.2.2.3. By End User
10.3.3. UAE Lysosomal Storage Diseases Therapeutics Market Outlook
10.3.3.1. Market Size & Forecast
10.3.3.1.1. By Value
10.3.3.2. Market Share & Forecast
10.3.3.2.1. By Treatment
10.3.3.2.2. By Indication
10.3.3.2.3. By End User
11. Market Dynamics
11.1. Drivers
11.2. Challenges
12. Market Trends & Developments
12.1. Recent Developments
12.2. Product Launches
12.3. Mergers & Acquisitions
13. Global Lysosomal Storage Diseases Therapeutics Market: SWOT Analysis
14. Porters Five Forces Analysis
14.1. Competition in the Industry
14.2. Potential of New Entrants
14.3. Power of Suppliers
14.4. Power of Customers
14.5. Threat of Substitute Product
15. PESTLE Analysis
16. Competitive Landscape
16.1. Pfizer, Inc.
16.1.1. Business Overview
16.1.2. Company Snapshot
16.1.3. Products & Services
16.1.4. Financials (In case of listed companies)
16.1.5. Recent Developments
16.1.6. SWOT Analysis
16.2. Sanofi SA
16.2.1. Business Overview
16.2.2. Company Snapshot
16.2.3. Products & Services
16.2.4. Financials (In case of listed companies)
16.2.5. Recent Developments
16.2.6. SWOT Analysis
16.3. BioMarin Pharmaceutical Inc
16.3.1. Business Overview
16.3.2. Company Snapshot
16.3.3. Products & Services
16.3.4. Financials (In case of listed companies)
16.3.5. Recent Developments
16.3.6. SWOT Analysis
16.4. Actelion Ltd.
16.4.1. Business Overview
16.4.2. Company Snapshot
16.4.3. Products & Services
16.4.4. Financials (In case of listed companies)
16.4.5. Recent Developments
16.4.6. SWOT Analysis
16.5. Raptor Pharmaceutical Corp.
16.5.1. Business Overview
16.5.2. Company Snapshot
16.5.3. Products & Services
16.5.4. Financials (In case of listed companies)
16.5.5. Recent Developments
16.5.6. SWOT Analysis
16.6. Protalix Biotherapeutics Inc.
16.6.1. Business Overview
16.6.2. Company Snapshot
16.6.3. Products & Services
16.6.4. Financials (In case of listed companies)
16.6.5. Recent Developments
16.6.6. SWOT Analysis
16.7. Amicus Therapeutics, Inc.
16.7.1. Business Overview
16.7.2. Company Snapshot
16.7.3. Products & Services
16.7.4. Financials (In case of listed companies)
16.7.5. Recent Developments
16.7.6. SWOT Analysis
16.8. Quest Diagnostics Inc.
16.8.1. Business Overview
16.8.2. Company Snapshot
16.8.3. Products & Services
16.8.4. Financials (In case of listed companies)
16.8.5. Recent Developments
16.8.6. SWOT Analysis
16.9. Amicus Therapeutics Inc.
16.9.1. Business Overview
16.9.2. Company Snapshot
16.9.3. Products & Services
16.9.4. Financials (In case of listed companies)
16.9.5. Recent Developments
16.9.6. SWOT Analysis
16.10. Shire Plc
16.10.1. Business Overview
16.10.2. Company Snapshot
16.10.3. Products & Services
16.10.4. Financials (In case of listed companies)
16.10.5. Recent Developments
16.10.6. SWOT Analysis
17. Strategic Recommendations
18. About Us & Disclaimer
- Not Sure / Need Reassuring
- Confirm Content
-
Content is provided by our partners and every effort is made to make Market Report details as clear as possible. If you are not sure the exact content you require is included in this study you can Contact us to double check. To do this you can:
Use the ‘? ASK A QUESTION’ below the license / prices and to the right of this box. This will come directly to our team who will work on dealing with your request as soon as possible.
Write to directly on support@scotts-international.com with details. Please include as much information as possible including the name of report or link so our staff will be able to work on you request.
Telephone us directly on 0048 603 394 346 and an experienced member of team will be on hand to answer.
-
- Sample Pages
-
With the vast majority of our partners we can obtain Sample Pages to support your decision. This is something we can arrange without revealing your personal details.
It is important to note that we will not be able to provide you the exact data or statistics such as Market Size and Forecasts. Sample pages usually confirm the layout or the Categories included in Charts and Graphs, excluding specific data.
To ask for Sample Pages by contact us through ‘? ASK A QUESTION’, support@scotts-international.com, or by telephoning 0048 603 394 346.
-
- Check for Alternatives
-
Whilst we try to make our online platform as easy to use as possible there is always the possibility that a better alternative has not been found in your search.
To avoid this possibility Contact us through ‘? ASK A QUESTION’, support@scotts-international.com, or by telephoning 0048 603 394 346 and a Senior Team Member can review your requirements and send a list of possibilities with opinions and recommendations.
-
- Confirm Content
- Prices / Formats / Delivery
- Prices
-
All prices are set by our partners and should be exactly the same as those listed on their own websites. We work on a Revenue share basis ensuring that you never pay more than what is offered elsewhere.
Should you find the price cheaper on another platform we recommend you to Contact us as we should be able to match this price. You can Contact us though through ‘? ASK A QUESTION’, support@scotts-international.com, or by telephoning 0048 603 394 346.
-
- Discounts
-
As we work in close partnership with our Partners from time to time we can secure discounts and assist with negotiations, this is part of our personalised service to you.
Discounts can sometimes be arranged for speedily placed orders; multiple report purchases or Higher License purchases.
To check if a Discount is possible please Contact our experienced team through ‘? ASK A QUESTION’, support@scotts-international.com, or by telephoning 0048 603 394 346.
-
- Available Currencies
-
Most Market Reports on our platform are listed in USD or EURO based on the wishes of our Partners. To avoid currency fluctuations and potential price differentiations we do not offer the possibility to change the currency online.
Should you wish to pay in a different currency to that advertised online we do accept payments in USD, EURO, GBP and PLN. The price will be calculated based on the relevant exchange rate taken from our National Bank.
To pay in a different above currency to that advertised online please Contact our team and a quotation will be sent within a couple of hours with payment details.
-
- Licenses
-
License options vary from Partner to Partner as is usually based on the number of Users that will benefitting from the report. It is very important that License ordered is not breached as this could have potential negative consequences for you individually or your employer.
If you have questions or need confirmation about the specific license we recommend you to Contact us and a detailed explanation will be provided.
-
- Global Site License
-
The Global Site License is the most comprehensive license available. By selecting this license, the Market Report can be shared with other ‘Allowed Users’ and any other member of staff from the same organisation regardless of geographic location.
It is important to note that this may exclude Parent Companies or Subsidiaries.
If you have questions or need confirmation about the specific license we recommend you to Contact us and a detailed explanation will be provided.
-
- Formats
-
The most common format is PDF, however in certain circumstances data may be present in Excel format or Online, especially in the case of Database or Directories. In addition, for certain higher license options a CD may also be provided.
If you have questions or need clarification about the specific formats we recommend you to Contact us and a detailed explanation will be provided.
-
- Delivery
-
Delivery is fulfilled by our partners directly. Once an order has been placed we inform the partner by sharing the delivery email details given in the order process.
Delivery is usually made within 24 hours of an order being placed, however it may take longer should your order be placed prior to the weekend or if otherwise specified on the Market Report details page. Additionally, if details have been not fully completed in the Order process a delay in delivery is possible.
If a delay in delivery is expected you will be informed about it immediately.
-
- Shipping Charges
-
As most Market Reports are delivered in PDF format we almost never have to add additional Shipping Charges. If, however you are ordering a Higher License service or a specific delivery format (e.g. CD version) charges may apply.
If you are concerned about additional Shipping Charges we recommend you to Contact us to double check.
-
- Prices
- Ordering
- By Credit Card
-
We work in Partnership with PayU to ensure payments are made securely in a fast and effortless way. PayU is the e-payments division of Naspers.
Naspers operates in over 133 International Markets and ranks 3rd Globally in terms of the number of e-commerce customers served.
For more information on PayU please visit: https://www.payu.pl/en/about-us
-
- By Money Transfer
-
If you require an invoice prior to payment, this is possible. To ensure a speedy delivery of the Market Report we require all relevant company details and you agree to maximum payment terms of 30 days from receipt of order.
With our regular clients deliver of the Market Report can be made prior to receiving payment, however in some circumstances we may ask for payment to be received before arranging for the Market Report to be delivered.
-
- By Credit Card
- Security
- Website security
-
We have specifically partnered with leading International companies to protect your privacy by using different technologies and processes to ensure security.
Everything submitted to Scotts International is encrypted via SSL (Secure Socket Layer) and all personal information provided to Scotts International is stored on computer systems with limited access in controlled environments.
-
- Credit Card Security
-
We partner with PayU (https://www.payu.pl/en/about-us) to ensure all credit card payments are made securely in a fast and effortless way.
PayU offers 250+ various payment channels and eWallet services across 4 continents allowing buyers to pay electronically, whether on a computer or a mobile device.
-
- Website security