What We Offer
Eva Nutra is a privately owned nutraceutical manufacturing company offering the ultimate in USP and cGMP contract manufacturing. We proudly provide quality manufacturing, competitive pricing, and quick turn-around times. Our in-house lab located in Las Vegas, Nevada, uses top-of-the-line machinery and experienced formulators to provide high-quality, efficient production capabilities from start to finish.
Vitamin and Supplement Production
Eva Nutra is capable of producing 50,000,000+ capsules per week with additional capabilities in tablets, including chewable and fast melts at a full-turn key capacity
Full Turn-Key and White Label Options
Eva Nutra can handle every aspect of the manufacturing process from concept to completion, or simply choose from our selection of pre-made formulations for your product.
Advanced Packing Solutions
Featuring three fully crewed high capacity lines with single serving packet and sample capabilities.
Custom Packaging
The design team brings your product to life with effective branding through unique labels, logos, and more.
State-of-the-Art Lab
Our USP certified lab is located in-house to maintain quality control while producing a variety of advanced multivitamins, botanicals, and nutraceuticals.
Quality Standards
Eva Nutra has a proven record of meeting the required industry GMPs for dietary supplements. Quality requirements at Eva Nutra demand that each product be consistent in identity, purity, strength, composition, and free of contaminants. Over 90 quality checkpoints are at work within our HEPA air filtered, climate controlled facility. Our relentless quality begins the moment ingredients are received at Eva Nutra. Incoming ingredients are first inspected before verifying their certificates of authenticity. Once verified, the ingredients undergo testing and screenings for odors, heavy metals, bacterial information, known contaminants, and concentration testing. The raw materials go through another round of testing and the products tested once more before being released. This guarantees the finished products will contain only what is on the label. Our knowledgeable personnel hold over 140 years of combined experience in nutraceutical manufacturing and are devoted to excellence in each product.
Specifications
Same as raw materials, we create specifications for each product which include purity/strength/composition test, contamination test (such as micro, heavy metals), weight variation, disintegration, and others.
Testing
The finished products are tested according to current specification by scientifically valid in-house methods (micro, heavy metal, mineral, weight variation, disintegration) or third party lab (HPLC, GC) to check if they meet label claims.
Stability
The stability testing is preformed to provide optimal storage conditions and expiration date.
Documentation
All finished product samples are related GMP documents are kept for future review and traceability.
In-House Lab
Eva Nutra’s state-of-the-art facility has the latest in equipment and technology. Each machine is hand selected for exceptional output capability and efficiency to provide quality products without compromise. Our current machines and technologies include:
Agilent 1260 Infinity II
Liquid Chromatography
One of the latest High Performance Liquid Chromatography machines (HPLC) available. HPLC is used to determine the purity and identity of organic compounds, and to specify the exact amount of phytochemicals present in plant extracts and all active ingredients in our products.
CAMAG High Performance Thin Layer Chromatography
Eva Nutra utilizes the most advanced form of thin-layer chromatography. This powerful analytical tool confirms and establishes the identity of every complex mixture and natural product that Eva Nutra manufactures
NEOGEN Soleris Next GenerationMicrobial Testing
This automated microbial testing machine uses advanced technology to test products for bacteria, yeast, mold, lactic acid and more in 48 hours instead of 5-7 days. This valuable tool helps us maintain quality, safety, and regulatory compliance.
Agilent 7900 ICP-MS
This technology enables our team to measure samples for heavy metals. Agilent's advanced matrix system allows for better trace level detection compared to other systems, ensuring that what's on the label is what's in the bottle.
PerkinElmer Frontier FTIR Spectrometer:
Fourier-Transform Infrared Spectroscopy (FTIR) technology is the starting point for samples in our lab. This machine uses infrared light to determine the identity of samples, allowing us to rule out contaminants and impurities to maintain quality control and consistency.
In-House Design
Bring your product to life with Eva Nutra’s design services for more effective branding. Our design team will help create eye-catching and FDA compliant assets ensuring that your information is presented in a concise, easy-to-interpret format.The design team brings your product to life through unique labels, logos, and more.
We are USP audited to confirm regulatory acceptance and verification of our manufacturing consistency and accuracy, assuring that nothing but top quality products are available to our customers. Our USP certified lab is located in-house and features the latest in quality control machinery such as the Agilent 7900 ICP-MS, CAMAG High-Performance Thin-Layer Chromatography, Agilent 1260 Infinity II Liquid Chromatography, Fourier-Transform Infrared Spectroscopy, microbial testing, and more.
Learn MoreUnited States Pharmacopeia (USP)
- Founded in 1820 to protect patients from poor-quality medicine.
- Before DSHEA, USP set the standards for acceptable “Nutritional supplements”
- Launched Dietary Supplement Verification Program in 2001 to combat quality inconsistencies in the market.
- USP focuses on Health Products (Pharmaceutical & Dietary Supplements)Formation of DSHEA recognized USP-NF standard as official but voluntary.
- USP published the Supplement Compendium (DSC) in 2009, to help the dietary industry ensure products meet spec entity, strength, quality, purity, packaging, and labeling.
- Retest/Spot Check conducted 1-6 times per year using samples purchased in stores.
- USP may preform testing beyond specified test on if there is probability that the product contains known contaminants.
- Tests for dissolution and disintegration.
- USP can conduct unannounced audits to check for compliance.
Turn Around Time
Eva Nutra understands that a rapid turnaround time is crucial when placing your order. We are outfitted for full turn-key manufacturing runs with turn-around times of 10-12 weeks from start to finish. State-of-the-art machinery housed within our 92,000 square foot facility provides for high-capacity production with output capability of 50,000,000+ capsules per week. The in-house lab in Las Vegas, Nevada has over 100 employees and a complete R&D staff to ensure production is completed fast, clean, and efficiently.
We are USP audited to confirm regulatory acceptance and verification of our manufacturing consistency and accuracy, assuring that nothing but top quality products are available to our customers. Our USP certified lab is located in-house and features the latest in quality control machinery such as the Agilent 7900 ICP-MS, CAMAG High-Performance Thin-Layer Chromatography, Agilent 1260 Infinity II Liquid Chromatography, Fourier-Transform Infrared Spectroscopy, microbial testing, and more.
Learn MoreUnited States Pharmacopeia (USP)
- Founded in 1820 to protect patients from poor-quality medicine.
- Before DSHEA, USP set the standards for acceptable “Nutritional supplements”
- Launched Dietary Supplement Verification Program in 2001 to combat quality inconsistencies in the market.
- USP focuses on Health Products (Pharmaceutical & Dietary Supplements)Formation of DSHEA recognized USP-NF standard as official but voluntary.
- USP published the Supplement Compendium (DSC) in 2009, to help the dietary industry ensure products meet spec entity, strength, quality, purity, packaging, and labeling.
- Retest/Spot Check conducted 1-6 times per year using samples purchased in stores.
- USP may preform testing beyond specified test on if there is probability that the product contains known contaminants.
- Tests for dissolution and disintegration.
- USP can conduct unannounced audits to check for compliance.
NSF International
- Founded in 1944 as National Sanitation Foundation but now currently known as NSF International.
- NSF provides accreditation services outside of dietary supplements, (i.e. automotive, construction, water, food, sustainability, etc.) They are like the jack of all trades, master of none.
- NSF suppliers standards that are traceable to USP.
- NSF-ANSI 173-03 Dietary Supplement Standards reference USP’s monographs.Retest/Spot Check conducted once a year with samples provided by manufacturer.
- Only tests for disintegration without disintegration.
- NSF is updating GMP Standard Certification with inputs provided from other agencies.
Experienced
Turn-Key Dietary
Supplement
Manufacturer
What We Offer
Eva Nutra is a privately owned nutraceutical manufacturing company offering the ultimate full service experience with the latest equipment technologies and highest quality standards without compromising the value our customers need to compete in the modern marketplace. We provide exceptionally high quality, competitive pricing and quick turn around times. Featuring a pharmacist led USP Certified full in-house lab located in Las Vegas, NV. We maintain an optimal manufacturing environment. We focus on superior quality and customer service to truly partner with our customers.
Vitamin and Supplement Production
Eva Nutra is capable of producing 50,000,000+ capsules per week with additional capabilities in tablets, including chewable and fast melts at a full-turn key capacity
Full Turn-Key and White Label Options
Eva Nutra can handle every aspect of the manufacturing process from concept to completion, or simply choose from our selection of pre-made formulations for your product.
Advanced Packing Solutions
Featuring three fully crewed high capacity lines with single serving packet and sample capabilities.
Custom Packaging
The design team brings your product to life with effective branding through unique labels, logos, and more.
State-of-the-Art Lab
Our USP certified lab is located in-house to maintain quality control while producing a variety of advanced multivitamins, botanicals, and nutraceuticals.
Quality Standards
Eva Nutra has a proven record of meeting the required industry GMPs for dietary supplements. Quality requirements at Eva Nutra demand that each product be consistent in identity, purity, strength, composition, and free of contaminants. Over 90 quality checkpoints are at work within our HEPA air filtered, climate controlled facility. Our relentless quality begins the moment ingredients are received at Eva Nutra. Incoming ingredients are first inspected before verifying their certificates of authenticity. Once verified, the ingredients undergo testing and screenings for odors, heavy metals, bacterial information, known contaminants, and concentration testing. The raw materials go through another round of testing and the products tested once more before being released. This guarantees the finished products will contain only what is on the label. Our knowledgeable personnel hold over 140 years of combined experience in nutraceutical manufacturing and are devoted to excellence in each product.
Specifications
Same as raw materials, we create specifications for each product which include purity/strength/ composition test, contamination test (such as micro, heavy metals), weight variation, disintegration, and others.
Testing
The finished products are tested according to current specification by scientifically valid in-house methods (micro, heavy metal, mineral, weight variation, disintegration) or third party lab (HPLC, GC) to check if they meet label claims.
Stability
The stability testing is preformed to provide optimal storage conditions and expiration date.
Documentation
All finished product samples are related GMP documents are kept for future review and traceability.
In-House Lab
Eva Nutra’s state-of-the-art facility has the latest in equipment and technology. Each machine is hand selected for exceptional output capability and efficiency to provide quality products without compromise. Our current machines and technologies include:
Agilent 1260 Infinity II
Liquid Chromatography
One of the latest High Performance Liquid Chromatography machines (HPLC) available. HPLC is used to determine the purity and identity of organic compounds, and to specify the exact amount of phytochemicals present in plant extracts and all active ingredients in our products.
CAMAG High Performance Thin Layer Chromatography
Eva Nutra utilizes the most advanced form of thin-layer chromatography. This powerful analytical tool confirms and establishes the identity of every complex mixture and natural product that Eva Nutra manufactures
NEOGEN Soleris Next GenerationMicrobial Testing
This automated microbial testing machine uses advanced technology to test products for bacteria, yeast, mold, lactic acid and more in 48 hours instead of 5-7 days. This valuable tool helps us maintain quality, safety, and regulatory compliance.
Agilent 7900 ICP-MS
This technology enables our team to measure samples for heavy metals. Agilent's advanced matrix system allows for better trace level detection compared to other systems, ensuring that what's on the label is what's in the bottle.
PerkinElmer Frontier FTIR Spectrometer:
Fourier-Transform Infrared Spectroscopy (FTIR) technology is the starting point for samples in our lab. This machine uses infrared light to determine the identity of samples, allowing us to rule out contaminants and impurities to maintain quality control and consistency.
In-House Design
Bring your product to life with Eva Nutra’s design services for more effective branding. Our design team will help create eye-catching and FDA compliant assets ensuring that your information is presented in a concise, easy-to-interpret format.The design team brings your product to life through unique labels, logos, and more.
We are USP audited to confirm regulatory acceptance and verification of our manufacturing consistency and accuracy, assuring that nothing but top quality products are available to our customers. Our USP certified lab is located in-house and features the latest in quality control machinery such as the Agilent 7900 ICP-MS, CAMAG High-Performance Thin-Layer Chromatography, Agilent 1260 Infinity II Liquid Chromatography, Fourier-Transform Infrared Spectroscopy, microbial testing, and more.
- Founded in 1820 to protect patients from poor-quality medicine.
- Before DSHEA, USP set the standards for acceptable “Nutritional supplements”
- Launched Dietary Supplement Verification Program in 2001 to combat quality inconsistencies in the market.
- USP focuses on Health Products (Pharmaceutical & Dietary Supplements)Formation of DSHEA recognized USP-NF standard as official but voluntary.
- USP published the Supplement Compendium (DSC) in 2009, to help the dietary industry ensure products meet spec entity, strength, quality, purity, packaging, and labeling.
- Retest/Spot Check conducted 1-6 times per year using samples purchased in stores.
- USP may preform testing beyond specified test on if there is probability that the product contains known contaminants.
- Tests for dissolution and disintegration.
- USP can conduct unannounced audits to check for compliance.
Turn Around Time
Eva Nutra understands that a rapid turnaround time is crucial when placing your order. We are outfitted for full turn-key manufacturing runs with turn-around times of 6-8 weeks from start to finish. State-of-the-art machinery housed within our 92,000 square foot facility provides for high-capacity production with output capability of 50,000,000+ capsules per week. The in-house lab in Las Vegas, Nevada has over 100 employees and a complete R&D staff to ensure production is completed fast, clean, and efficiently.