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Our Services

Human safety isn’t expensive, it is priceless

Avoid costly recalls and potential safety issues, partner with ARL-EuTech to ensure compliance.

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Pharmaceutical

ARL-EuTech is the laboratory for many pharmaceutical companies. Our highly experienced team has been providing analytical services to the pharmaceutical industry for eighteen years. Work is conducted in our state-of-the-art facilities.

ARL-EuTech skilled staff has been working hand-in-hand with pharmaceutical companies. Our knowledge-based company will become an extension of your own laboratory. Our services performed are done under strict confidentiality. ARL-EuTech services are conducted in our state-of-the-art facilities and performed under GLP/cGMP guidelines of the FDA. Keep in mind, safety is not expensive it is priceless!

Contact us for the following services:

Separation and Identification

  • Impurities
  • Metabolites
  • Degradation products
  • Unknown compounds
  • Co-eluting compounds
  • Chiral compounds
  • Residual solvents
  • USP 232/233/2232

Extractables/Leachables

  • Developing routine extractable methods
  • Extraction utilizing USP protocols
  • Extractable/Leachable evaluations
  • Extractable screening
  • Scientific instruments & laboratory consumables
  • Characterization of extractables
  • Simulation study
  • Toxicology assessment
  • FDA extraction testing and controlled extraction
  • Ensuring the compatibility of drug and closure packaging
  • Ensuring safety relative to packaging
  • Adulterants that may enter the supply chain instrumentation used to analyze extracts (GC-MS, LC-MS, HPLC, FT-IR, ICP-MS).

Stability Testing

  • Accelerated stability
  • Degradation kinetics
  • Identification of degradation products
  • Shelf life

Raw Material Testing

  • Loss on drying
  • Heavy metals
  • Full Monograph Testing
  • Impurity testing
  • Appearance
  • Molecular Weight Determination
  • Deformulation
  • Many other analytical tests using (GC-MS, LC-MS, HPLC, FT-IR, ICP-MS, etc.)

Release Testing

  • Method development and validation
  • Method verification and transfer
  • cGMP drug release testing
  • Compendial testing

Compounding Pharmacies/Hospitals

  • Solving FDA Related Issues
  • Anti-Factor IIA potency as per USP monograph for heparin sodium
  • Verification of USP methods
  • Stability testing

Heparin/LMWH

  • Anti-Factor IIA potency
  • Verification of USP methods
  • EP and USP monograph testing

Method Development and Validation

EuTech Scientific Services, Inc. has over two decades of experience in method development and validation. Our expert technical staff enables us to develop and validate specialized methods of analysis for a number of products such as yours. We adhere to GLP guidelines provided by the FDA. Our state of the art laboratory is equipped to meet all your analytical needs.

EuTech Scientific Services can be entrusted with all your method development and validation projects. Our protocols are flexible and can be designed to meet your specific needs. EuTech staff prides itself on providing accurate, dependable data in a timely, cost and effective manner.

Analytical Characteristics Used to Define Our Method Validation:

  • Accuracy
  • Precision
  • Specificity
  • Detection Limit
  • Quantitation Limit
  • Linearity
  • Range
  • Robustness

Contact us for the following services:

  • Chromatographic Techniques including: HPLC, GC, GC-MS/MS, LC-MS/MS, ICP-MS and FTIR Spectroscopy
  • Protocol Validation and transfer
  • Residual Solvents
  • Extractables/Leachables Studies
  • Trace Organics
  • Forced degradation studies
  • Stability Studies
  • Details of active ingredients
  • Impurity profiling and identification
  • Heparin
  • Cannabis

Medical Devices

EuTech Scientific Services, Inc. serves medical device companies by aiding in the development of their quality assurance program of medical devices and in their research and development.

We understand the medical device industry needs very well. Our skilled staff has been working hand-in-hand with medical devices for more than two decades. We offer the highest quality comprehensive service.

EuTech is fully compliant with GLP regulations. All work is performed in strict confidentiality.We accept Research and Method Development contracts from Medical Device companies for their products/methods.

Products

We perform research projects to improve existing products or introduce a complete new line of products. Our services in this area are very extensive and have resulted in state-of-the-art and unique products. We assure you the quality of our work.

Methods

We perform research in changing or revising existing methods to improve the process, reduce costs, and minimize procedure time. We perform verification or validation of the methods as required.

Contact us for the following services:

Analysis

  • Residue Quantification
  • Binding Assays
  • Extractable and leachable Testing
  • Formulation and Process Development
  • Regulatory and Compliance Support
  • Litigation Support
  • Containers and Closures Testing
  • Physico-Chemical Testing

Physico-Chemical Testing

  • Pore size distribution and bubble point
  • Gas and liquid permeability
  • Material/chemical characterization
  • Compressibility
  • Resilience
  • Filter integrity
  • Water uptake
  • Durometry
  • Plastometry
  • Spectrophotometry
  • Photolysis
  • Calorimetry

Stability

  • Shelf life
  • Accelerated aging
  • Verification of compatibility of ingredients and packaging composition
  • Controlled temperature and humidity across a wide range of conditions

Cannabis and Hemp

    Hemp/cannabis analytical services

  • Cannabinoid profile
  • Heavy metals
  • Pesticides
  • Potency
  • Quantitation and relative Ratio of CBD and THC
  • Residual solvent
  • Moisture content
  • Terpene profile
  • Microbiology

Our experienced scientific team have validated methods in hand to analyze your hemp and CBD products in all matrices. Many of our clients have engaged us to follow the quality from origin in farm to processing to final product. This allows us to ensure the quality, safety and safeguarding the potency of every step of the way.

Our mission is to ensure the safety and the quality of your Cannabis and Hemp products. ARL-EuTech staff prides itself in providing accurate, dependable data in a timely, and cost effective manner. Please feel free to contact us to help you out for setting up your quality program for all your hemp and related products from beginning to the end product. Our skilled staff has all the expertise and experience to take care of your all analytical chemistry needs utilizing our state of the art laboratories and Instrumentation.

We have pick up and sample collection service if needed and have the DEA license for schedule I to V.

Environmental Analysis

The environmental division of ARL-EuTech is Complete Analysis Laboratories (CALI) located in Highland Park, NJ. CALI is one of the most experienced laboratories in the United States for more than three decades. In 2015 ARL-EuTech acquired CALI assets. Combining the resources of the two companies allows professional handling of all analytical chemistry customers.

Certifications

CALI is an NJDEP Certified Environmental Laboratory# 12070, Our staff prides itself on providing accurate, dependable data in a timely, cost and effective manner. Our lab is committed to developing partnerships with our clients.

We invite you to contact CALI Labs to explore ways we can provide answers for a challenging analytic Environmental project. We are determined that our staff is capable of customizing services and methods that fulfills your inquiries.

Pickup Services

We will come to your facility to pick up grab samples or set up samplers to collect samples. You share your agreement with the state for the type of testing and frequency your business is required by New Jersey State and we will set up the logistics and collect samples and give you results in time to remain compliant and avoid any unnecessary fine.

Services We Provide

  • Elemental microanalysis
  • Environmental analysis
  • Soil testing
  • Chemical testing
  • Waste water analysis
  • Drinking water analysis

Clients

  • Schools and daycares
  • Hospitals
  • Manufacturing industries
  • Local businesses generating waste water

Complete USP Micro Testing

Microbiological analysis is one of ARL’s “bread and butter” operations. Since its genesis in 2000, ARL has built its success around testing accuracy and on-time reporting. We offer BAM, AOAC, and USP methods, including USP 2021/2022, USP 51, USP 61/62, and USP 71. We have the experience to help you select the most appropriate method for your product and determine your acceptance criteria. Our expertise will add another level to your quality control and quality assurance programs. No matter your quality objectives, ARL’s team will help you achieve success.

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