openPR Logo
Press release

Homeopathy Products Market Proposals & Trends Leading to 18.2% CAGR Growth during 2017-2026

05-30-2018 02:29 PM CET | Health & Medicine

Press release from: Fact.MR

Fact.MR

Fact.MR

Growing awareness of alternative medicine has presented huge pathway for growth in adoption of homeopathy products. Individuals across the globe are opting for effective yet natural medications that offer permanent healing without side effects. People are more inclined towards medications, for instance homeopathy, that offer permanent cure to avoid unnecessary healthcare costs and inconvenience.

Request For Sample Report @ https://www.factmr.com/connectus/sample?flag=S&rep_id=604

This has led to an upsurge in the use of alternative medicines, and in turn supported the growth in sales of homeopathy products. This has offered companies involved in manufacturing and distribution of homeopathy products an upward growth path with increasing number of patients preferring homeopathy over invasive medications and allopathy.

According to analysis carried out by Fact.MR, the global market for homeopathy products is poised to expand at a high value CAGR during the period of assessment, 2017-2026. By end of the year of assessment (2026), the sales of homeopathy products are estimated to touch a valuation of more than US$ 23 Bn and is projected to expand at a volume CAGR of 17.1% during the period of forecast. This growth in sales of homeopathy products is mainly driven by rising awareness of homeopathy treatment and increasing preference for zero side effect medications and economical but effective drugs.

Protect Consumers Who Chose Alternative Remedies – FDA’s New Approach Towards Regulating Homeopathic Drugs

Food and Drug Administration is looking forward to introduce “risk based enforcement approach” to drugs that are labelled homeopathic in the America market. With a view to protect patients that prefer homeopathic products, FDA is to update current policy to address situations wherein homeopathic treatments are marketed especially for serious conditions or diseases, but the products have not offered clinical advantages. This new policy would cover all products that are labelled homeopathic but contain potentially dangerous and unsafe ingredients or which are do not follow standard manufacturing practices.

FDA’s approach to regulate homeopathic products would reflect the present criticality and complexity of the entire market. Few examples of products that could be subject to FDA’s enforcement approach are children’s and infant products that are labelled to comprise ingredients related to potentially significant concerns associated with safety, for instance nux vomica and belladonna; as well as products that are being marketed for serious maladies such as heart diseases and cancer.

Increasing Inclination Towards Non-Invasive Remedies to Spur Sales of Homeopathic Products

Invasive treatments to cure disorders and malignancies are considered as last resort by people, who are more focused on using alternative medications such as naturopathy and homeopathy. With growing demand for medications that are to be consumed orally, supported by increasing preference for orally administered medications and drugs that are exempt of side effects, consumption of homeopathy products is set to increase in the coming years.

Browse Full Report with TOC @https://www.factmr.com/report/604/homeopathy-products-market

Allopathy also includes strong drugs, but are not suitable for every individual. Moreover, with respect to costing, allopathic medications are highly priced and showcase temporary effect on the illnesses. The illness can return even after the dosage of the prescribed drug is over. Cases of drug abuse is another fact, owing to which people are shifting towards natural medications. Homeopathy products offer preventive measures, boost immune systems, are inexpensive and do not have side effects. This is expected to spur the sales of homeopathy products in the years to follow.

The global market for homeopathy products is highly competitive and consists of numerous international and regional vendors. Competitive environment in homeopathy products market is expected to intensify in the years to follow with growth in innovations and product line extensions based on treatment of various disorders and ailments. Key participants in the global homeopathy products market include Boiron Group, Biologische Heilmittel Heel GmbH, A Nelson & Co Ltd., GMP Laboratories of America, Inc., and Standard Homeopathic Company (Hyland’s, Inc.), to name a few.

Check Discount @ https://www.factmr.com/connectus/sample?flag=D&rep_id=604

About Fact.MR

Fact.MR is a fast-growing market research firm that offers the most comprehensive suite of syndicated and customized Healthcare Market Research Reports. We believe transformative intelligence can educate and inspire businesses to make smarter decisions. We know the limitations of the one-size-fits-all approach; that's why we publish multi-industry global, regional, and country-specific research reports.

Contact Us

Fact.MR
11140 Rockville Pike
Suite 400
Rockville, MD 20852
United States
Email: sales@factmr.com
Web: https://www.factmr.com/Get More Industry Insights At: https://www.linkedin.com/company/factmr

This release was published on openPR.

Permanent link to this press release:

Copy
Please set a link in the press area of your homepage to this press release on openPR. openPR disclaims liability for any content contained in this release.

You can edit or delete your press release Homeopathy Products Market Proposals & Trends Leading to 18.2% CAGR Growth during 2017-2026 here

News-ID: 1066173 • Views:

More Releases from Fact.MR

Bioinformatics Market is Growing at a CAGR of 13.4% by 2034 | Fact.MR Report
Bioinformatics Market is Growing at a CAGR of 13.4% by 2034 | Fact.MR Report
The latest report on the Bioinformatics Market, projecting robust growth driven by the increasing demand for genomic research, advancements in artificial intelligence (AI), and the rising adoption of precision medicine. Valued at USD 14.29 billion in 2024, the global market is forecast to expand at a compound annual growth rate (CAGR) of 13.4%, reaching USD 50.25 billion by 2034. This significant growth underscores the critical role of bioinformatics in decoding
Residential Robotic Vacuum Cleaner Market to Reach USD 11.6 Billion by 2033 | Key Players: iRobot Corporation, Neato Robotics, Inc., Yujin Robot, Co., Ltd., and Dyson Inc
Residential Robotic Vacuum Cleaner Market to Reach USD 11.6 Billion by 2033 | Ke …
Fact.MR today released its latest report on the Residential Robotic Vacuum Cleaner Market, projecting robust growth driven by increasing demand for automation, busy lifestyles, and advancements in smart home technologies. Valued at USD 3.0 billion in 2023, the global market is forecast to expand at a compound annual growth rate (CAGR) of 14.4%, reaching USD 11.6 billion by 2033. This significant growth highlights the rising adoption of robotic vacuum cleaners
Brain-Computer Interface Market is Estimated to Reach USD 6.5 Billion by 2033
08-29-2025 | Health & Medicine
Fact.MR
Brain-Computer Interface Market is Estimated to Reach USD 6.5 Billion by 2033
The global brain-computer interface (BCI) market was valued at USD 1.6 billion in 2022 and is projected to reach USD 6.5 billion by 2033, growing at a compound annual growth rate (CAGR) of 13.6% from 2023 to 2033. This expansion reflects the increasing adoption of BCI technologies in medical applications, driven by advancements in neuroscience, AI, and sensor technologies. BCIs enable direct communication between the brain and external devices, offering
Orally Disintegrating Tablet Market is Projected to Reach USD 72.68 Billion by 2034 | Key Players: Johnson & Johnson Services Inc; Teva Pharmaceutical Industries Ltd.; Sun Pharmaceutical Industries Ltd.; Takeda Pharmaceutical Company Limited
08-29-2025 | Health & Medicine
Fact.MR
Orally Disintegrating Tablet Market is Projected to Reach USD 72.68 Billion by 2 …
The global orally disintegrating tablet (ODT) market is valued at USD 24.45 billion in 2024 and is forecasted to expand at a compound annual growth rate (CAGR) of 11.5%, reaching USD 72.68 billion by 2034. This robust growth is driven by the increasing demand for patient-friendly dosage forms, particularly among the elderly, pediatric, and dysphagic populations, who benefit from ODTs' ease of administration without water and rapid dissolution. ODTs enhance

All 5 Releases


More Releases for FDA

DreaMed receives 5th FDA Clearance
TEL AVIV, Israel: DreaMed Diabetes LTD. ("DreaMed" or the "Company"), developer of the endo.digital Clinical Decision Support System announced today that it has received its 5th U.S Food and Drug Administration (FDA) clearance that expands the scope of AI enhanced treatment recommendations to patients on fixed meal insulin regimens. endo.digital is the first decision support system that has been cleared to assist healthcare providers in the management of diabetes
FDA Compliant Blood Storage and Preservation
Accsense Monitoring System Automates Data Archive and Alarming CAS DataLoggers provided the temperature alarming and monitoring system to a hospital blood bank looking to replace their old paper chart recorders as they became unreliable and spare parts were harder to find. For proper blood storage and preservation, the lab’s medical units needed to maintain storage temperatures between 2°C to 6°C (36°F to 43°F), given the perishability of blood components. The facility
FDA grants orphan drug status to Vicore
US Food and Drug Administration has awarded Vicore Pharmaceuticals with orphan Drug designation for the treatment of Idiopathic Pulmonary Fibrosis (IPF). FDA’s Orphan Drug Designation program provides certain incentives for companies developing therapeutics to treat rare diseases or conditions, defined as those affecting less than 200,000 individuals in the U.S. A drug candidate and its sponsor must meet several key criteria in order to qualify for, and obtain, orphan drug
New FDA Design Control Training Courses
Salt Lake City, Utah - February 23 2017 - Procenius Consulting is a medical device consulting firm specializing solely in medical device design controls regulation (21 CFR 820.30). Announcing New Design Control Training Courses Procenius Consulting has just launched two new training courses covering basic and advanced topics of medical device design control regulation. These courses focus on compliance, practical implementation and industry best practices techniques for developing or improving a
fda online training
GRC Training Solutions provides end-to-end FDA compliance solutions for those companies who want to maximize security, minimize operational costs, improve staff productivity and stay on top of all their compliance documentation. GRC Training Solutions boasts a team of experts and specialists who have a proven track record in working with the biotechnology, medical device, diagnostic and pharmaceutical fields. Our team will work with you closely and develop solutions that meet
11-09-2016 | Science & Education
GRCTS
FDA online training
Description: Device firms, establishments or facilities that are involved in the production and distribution of medical devices intended for use in the U.S are required to register annually. Most establishments that are required to register with the FDA are also required to list the devices that are made there and the activities that are performed on those devices. Initially, FDA issued a 28-page Proposed Rule that would amend its regulations regarding