Eurofins US

The business focuses on providing technical studies and regulatory consultancy to help manufacturers, agri‑tech innovators, plant breeders and the seed industry bring new solutions to market and keep existing products compliant.

Core service areas

• Field and laboratory studies for plant protection products

Conducting GLP‑compliant field and lab studies to determine the safety and efficacy of new chemical and bio‑rational crop protection products.

• Agrochemical registration support

Designing and executing study programmes and providing expert interpretation to support agrochemical registration dossiers and responses to data call‑ins.

• Regulatory consultancy and due diligence

Tailored technical and regulatory due diligence for ag‑biotech and crop protection investments, helping to de‑risk innovation and support market access.

• Seed technologies and plant breeding support

Integrated solutions for plant breeders and the seed industry from R&D through to marketing new varieties.

• REACH and chemicals-related testing

Studies and guidance to support REACH and other chemical safety frameworks where they intersect with agricultural products.

Industries served

The Agroscience Services page lists several broad industries:

• Agriculture – end‑to‑end services to develop, register and maintain sustainable agricultural innovations.
• Biocides / non‑crop pest control – efficacy and safety testing for household pest control, public health vector control and professional pest management products.
• Chemicals – studies and guidance for industrial and specialty chemical manufacturers seeking compliant market access.
• Pharmaceuticals – environmental risk assessment (ERA) programmes for human and veterinary medicinal products.

Safety and assessment focus areas

The service descriptions group technical expertise into:

• Biological assessment – understanding product performance and impact in biological systems.
• Consumer and human safety – assessing potential risks to users and bystanders.
• Environmental safety – evaluating effects on soil, water, non‑target organisms and wider ecosystems.
• Product chemistry – characterising active ingredients and formulations to meet regulatory expectations.

What the page does not publish

• It does not state which specific studies are performed by which laboratory or field station, or which regions individual sites cover.
• It does not provide any prices, fees, rate cards, cost ranges, or example quotes.
• It does not state turnaround times, capacity, or detailed study protocols.

Anyone needing details on a particular study type, location, capacity, timing or pricing must contact Eurofins Agroscience Services directly through the site's contact options or via a relevant business contact.

Overview

The Assurance and Inspection Services page for North America presents Eurofins as a partner to help businesses manage compliance, quality and safety risks early, particularly in the food, consumer product, healthcare and cosmetics sectors.

Services are organised around sustainability, audit and certification, inspection and quality assurance, training, labelling support and advisory work. The page also emphasises that certification activities are carried out by independent Certification Bodies and that impartiality is protected.

Key service areas

Sustainability services

Support for environmental and social responsibility programmes, including:

• Zero Waste to Landfill Certification – designed for manufacturing industries.
• Better Cotton – third‑party verification services to support Better Cotton Initiative (BCI) commitments.
• amfori BEPI – programmes aimed at reducing environmental impact and improving operational efficiency.
• GOTS and Textile Exchange certification – accredited certification services for GOTS and Textile Exchange standards (GRS, OCS, RCS and CCS).
• ZNU Standard – assessment of company‑wide sustainable management systems.

Audit and certification

Independent audit and certification services, including:

• Ethical and social responsibility audits.
• Environmental audits.
• Food, feed and agriculture audits.
• Pharmaceutical, food and dietary supplement compliance audits.
• Cosmetic and OTC drug compliance audits.

(The page notes that certification activities are managed separately from consulting work to maintain impartiality.)

Quality inspection services

Inspection solutions aimed at assessing product quality and conformity throughout production, for example:

• Fabric inspection.
• Product inspection (pre‑production, inline, during production and final random inspection).
• Supplier self‑inspection programmes.
• Video inspection and remote witnessing.
• Inspection Combo and Inspection Studio options.

QA–QC programme for garment industry

A modular, highly cost‑effective quality assurance and quality control programme for garment and apparel supply chains, described as a 12‑module system that can be customised.

Training

Training is offered separately from audit and certification work and does not guarantee certification. Topics include:

• Food safety and quality.
• Healthcare.
• Dietary supplement training.
• E‑learning platforms.
• Higg FEM.
• Social and Labor Convergence Program.
• Wastewater and effluent treatment plants.

Labelling and advisory

• Food and dietary supplement labelling – support to help meet regulatory labelling requirements in different markets.
• Advisory services – independent advisory teams for food, pharmaceutical, cosmetic and other industries, focused on process improvement and risk management.

Industries served

The page lists a broad range of product categories and sectors, including:

• Garments, textiles and footwear.
• Toys, baby and children's products.
• Furniture and hardgoods.
• Pharmaceutical.
• Food.
• Dietary and food supplements.
• Cosmetics.
• Feed and agriculture.
• Electrical and electronics products.
• Business and industrial products.
• Packaging.

What the page does not publish

• It does not specify pricing, fees, cost ranges or example quotes for any audit, inspection, certification or training.
• It does not state exact audit durations, lead times, or capacity by region.
• It does not list detailed programme requirements beyond the brief summaries above.

For details of scope, availability, timelines and pricing, customers are directed to contact Eurofins Assurance and Inspection Services through the site's contact options.

Overview

The Eurofins BioPharma Services network is described as a first‑class biopharmaceutical and medical device services partner. It supports pharmaceutical, chemical, biotechnology, medical device and cosmetic companies through an international network of laboratories and testing units with global reach and harmonised quality systems.

Service offerings span discovery through to commercialisation, with specialist capabilities grouped into:

• Bioanalytical Services.
• BioPharma Central Laboratory.
• BioPharma Product Testing.
• CDMO (Contract Development and Manufacturing Organisation) services.
• Discovery services.
• Medical Device Services.
• PSS Insourcing Solutions.

Services by development phase

Discovery

Support for early‑stage R&D, including:

• Eurofins Discovery – a global CRO offering a large portfolio of products and services to drug discovery researchers, based on decades of industry experience.
• Medical Device Services – regulatory compliance expertise and GMP/GLP/ISO 17025 testing for medical devices.
• PSS Insourcing Solutions – Eurofins teams placed directly at client sites to run laboratory operations under long‑term partnership models.

Preclinical and early development

Services aimed at assessing the safety and biological activity of candidate products:

• Bioanalytical Services – assay development, validation and sample analysis for PK/TK, ADA, NAb and biomarker studies in preclinical and clinical settings.
• BioPharma Product Testing – GMP testing for a wide range of modalities including ADCs, biotherapeutics, cell and gene therapies, mAbs, mRNA/NATs, oncolytic viruses, peptides, small molecules and therapeutic proteins.
• CDMO – development and manufacturing support for biologics and small molecules.
• Medical Device Services – testing to help meet regulatory safety and performance requirements.
• Preclinical and Early Development – integrated bioanalysis and early phase clinical support.
• PSS Insourcing Solutions – on‑site scientific teams supporting preclinical and early development operations.

Clinical research and development

Support for Phase I–III clinical studies:

• Anatomical pathology – histopathology evaluation and related services for preclinical and clinical research.
• Bioanalytical Services – continued PK/TK, ADA, NAb and biomarker support in clinical trials.
• BioPharma Product Testing – GMP testing of clinical supplies.
• Central Laboratory – global CAP‑accredited central labs providing safety, efficacy, biomarker and pathology services for trials in over 85 countries.
• CDMO – manufacturing support for clinical‑stage products.
• Early clinical development – scientific capabilities to support first‑in‑human and early phase studies.
• Medical Device Services – compliance testing for devices used in clinical investigations.
• PSS Insourcing Solutions – embedded teams supporting clinical trial operations.
• Specialty clinical trial laboratories – advanced expertise in infectious disease, immunology, molecular testing and cell and gene therapy, with global logistics.

Approval

Services to verify safety, effectiveness and controls ahead of marketing authorisation, using many of the same capabilities as in the clinical and product testing stages (anatomical pathology, product testing, central lab, CDMO, medical device services, PSS and specialty clinical trial labs).

Commercial and post‑approval

Support for post‑marketing surveillance, quality control and long‑term effectiveness studies, again drawing on:

• Anatomical pathology.
• BioPharma Product Testing.
• CDMO.
• Central Laboratory.
• Medical Device Services.
• PSS Insourcing Solutions.
• Specialty clinical trial laboratory expertise.

What the page does not publish

• It does not provide prices, fees, rate cards, cost ranges or example quotes for any service.
• It does not specify individual laboratory locations or their detailed scopes of accreditation for each method.
• It does not state timelines, capacity limits or guaranteed turnaround times.
• It does not give medical or regulatory advice on whether a particular development strategy will be approved.

For concrete project plans, pricing, study designs or regulatory strategies, the site directs prospective clients to contact Eurofins BioPharma Services directly through the contact options provided.

Directory entries that are published pair a company name, a full address and a business line — for example Eurofins Environment Testing Southeast, LLC at 481 Newburyport Avenue, Altamonte Springs FL 32701, and Eurofins Diatherix Laboratories, LLC at 601 Genome Way, Suite 2100, Huntsville AL 35806.

Contact is by web form per business line. The Environment Testing form asks for full name, city, state, phone number, company, email address, message, country and business line. No opening hours, appointment booking, scheduling tool, price list, rates or fees are published anywhere on the pages read.

The page names the clinical companies in this network: Eurofins Clinical Enterprise, described verbatim as a "CLIA-certified, CAP-accredited lab delivering multiomic testing with integrated data solutions"; Eurofins CellTx; Eurofins Diatherix; Eurofins Genomics; Eurofins Viracor; Eurofins DPT; and Eurofins Transplant Genomics. No accreditation or certification statement beyond that one line about Eurofins Clinical Enterprise is published on this page.

Nothing on the site says what any test result means, whether a person should be tested, how accurate a result is, or when a result will be back. Those are medical determinations and belong with the ordering clinician and the performing laboratory. Anyone asking about their own health, a result, a referral, or whether a test is appropriate should be directed to their clinician and to the specific Eurofins laboratory handling the sample. The page publishes no prices, no cost or fee information, no insurance coverage terms, and no phone number, appointment booking or scheduling tool.

The service groups are

Sustainability Services, listing Chem-ST chemical smart testing, PFAS testing, Total Organic Fluorine (TOF) testing, Origin ID, EUDR deforestation impact assessment, DPP preparation and recycled plastics testing; Testing, covering chemical, physical, mechanical, clinical, environmental, electrical safety and performance testing; Certification and approvals, for softlines and hardlines, electrical and electronics, and construction and building; Expert services and regulatory services, covering regulatory programmes and technical compliance files; Inspections and audits, covering product inspections and environmental, social, technical and security audits; Consumer research and sensory evaluation; and Training, described as industry-specific regulatory and technical courses.

Related pages linked from the same section include Cosmetics and Personal Care, Softlines and Hardlines, Electrical and Electronics, Sustainability Services, SPF testing for sun care products, and SMETA audits, described on the home page as "SMETA 2-pillar and 4-pillar audits".

The page does not publish prices, pricing, rates, fees, cost ranges or quote and estimate figures for any test, inspection, certification or course, and it does not state which laboratory or location performs a given service, what a testing scope covers for a particular product, or how long any of it takes. Contact is by the "Contact us" form on the page; no direct phone number, address or opening hours is printed.

That list is the full extent of what the page publishes about scope. It does not say which of these a particular laboratory performs, what sample types or matrices are accepted, what methods or reporting limits apply, or how long analysis takes. It publishes no price, pricing, cost, rate or fee information, and no quote or estimate figures.

Contact for this business is through a form at eurofins.com/en-us/environment-testing/contact-us/. The form asks for full name, city, state, phone number, company, email address, message, country and business line, with consent checkboxes for data processing and tracking technologies. There is no phone number, email address, street address or opening hours printed on the contact page itself, and no online booking or appointment scheduling tool. A request for a quote, a price, an estimate, sample containers or a sampling schedule has to be made through that form or through a specific laboratory found with the site's location finder.

The page also names industries served, including baby food, beverages, botanicals, milk and dairy, food service and quick-serve restaurants, grain inspection, hemp and CBD products, infant formula, and food ingredients and spices.

No prices, rates, fees, cost figures or quote or estimate amounts are published for any of this, and the page does not say which laboratory location performs which analysis. Contact is by the page's contact form.

These are different businesses run from different laboratories, so an answer about one does not carry over to another. Environmental sample analysis, food safety work, clinical diagnostic testing, forensic services and consumer product testing each belong to a different Eurofins company, and anyone making contact should name the business line they need; the site's contact forms ask the sender to select one.

The site does not publish prices, a price list, rates, fees, cost ranges, or any quote or estimate figure for any service, and it publishes no general phone number for the US organisation. It does not state any individual laboratory's scope of testing, whether a particular sample can be tested, or how long results take. Those questions go to the relevant Eurofins business through its contact form, or to a laboratory found with the site's own location finder.

Ask anyway — the agent will say plainly that it is not published rather than guess.