American Preclinical Services of Minneapolis, MN at MEDICA 2017 in Düsseldorf -- MEDICA Trade Fair
Service

American Preclinical Services

8945 Evergreen Blvd., 55433 Minneapolis, MN
USA

Telephone +1 763 7177990
Fax +1 763 7172042
quoting@apsemail.com

This company is co-exhibitor of
Minnesota Trade Office

Hall map

MEDICA 2017 hall map (Hall 16): stand A18

Fairground map

MEDICA 2017 fairground map: Hall 16

Our range of products

Product categories

  • 07  Medical Services and Publications
  • 07.10  Technical equipment management, Test houses / Certification Bodies

Technical equipment management, Test houses / Certification Bodies

  • 07  Medical Services and Publications
  • 07.10  Technical equipment management, Test houses / Certification Bodies
  • 07.10.01  Biocompatibility testings

Biocompatibility testings

Our products

Product category: Technical equipment management, Test houses / Certification Bodies, Biocompatibility testings

In-vivo Testing

APS offers an array of in-vivo testing. We have both large and small animal capabilities with numerous study designs that can be used for biocompatibility evaluations. Let our experienced staff help you select or design the right in-vivo tests to meet all of your requirements.

Sensitization Testing
  • Guinea Pig Maximization
  • Buehler
  • Murine Local Lymph Node Assay (LLNA)
Implantation Testing
  • Subcutaneous Implant
  • Intramuscular Implant
Irritation Testing
  • Intracutaneous Reactivity 
  • Vaginal Mucosal Irritation
  • Systemic Toxicity Testing
  • Materials Mediated Pyrogenicity
  • Acute Systemic Toxicity
  • Sub-acute Toxicity
  • Sub-chronic Toxicity
  • Chronic Toxicity
In-Vivo Thrombogenicity Testing
  • Canine, Porcine, Ovine, Bovine
  • 4hr, 72hrs
  • Standard and Custom Designs

Not all in-vivo thrombogenicity studies are created equal.

As the designs of medical devices continue to become more advanced, the overall placement of the device challenges traditional methods. Currently, devices subject to a standard thrombogenicity test are typically placed into the jugular vein with minimal concern as to the impact of blood flow, fit or placement. In reality the traditional design lacks the ability to ensure a proper placement of a device and it is not possible to confirm that proper blood flow has been maintained prior to starting the four-hour indwelling period.

The in-vivo thrombogenicity studies are especially challenging tests for many labs to conduct, given the required equipment, in-house technical expertise and implantation methodologies needed. APS offers you these services, plus superior surgical and interventional deployment techniques using fluoroscopy, which makes the test more reliable and reproducible.

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Product category: Technical equipment management, Test houses / Certification Bodies, Biocompatibility testings

In-vitro Testing

American Preclinical Services has a broad range of in-vitro testing services. We offer multiple methodologies that can be used for the evaluation of biocompatibility, toxicology and lot-release testing. Depending on your regulatory requirements, our in-vitro services offer tests that meet ISO 10993, USP <87>, and JMHLW guidelines.

We are passionate about offering alternative methods that can be used for the evaluation of your product. If you have a specific test methodology that may not be in our current scope, please contact us today to discuss availability and/or a validation plan to meet all of your testing needs.

Cytotoxicity Testing
  • Agar Overlay
  • Direct Contact
  • MEM Elution
  • Neutral Red Uptake
  • MTT
  • Limulus Amebocyte Lysate (LAL)

Genotoxicity Testing
  • AMES (Bacterial Mutagenicity)
  • Chromosome Aberration
  • Mouse Lymphoma Assay
  • Mouse Micronucleus Assay (Peripheral Blood Method)

Hemocompatibility Testing
  • Hemolysis (ASTM, USP and JMHLW)
  • Complement Activation C3a and SC5b Assay
  • Partial Thromboplastin Time (PTT)
  • Prothrombin Time Assay (PT)
  • Platelet and Leukocyte
  • In-vitro Blood Loop

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About us

Company details

Discover American Preclinical Services (APS)

APS is a State of the Art, AAALAC and ISO17025 accredited, USDA registered and GLP compliant Contract Research Organization (CRO) located in Minneapolis, MN specializing in medical device and pharmaceutical testing.

By utilizing our catalogue of services, which includes regulatory consulting, ISO10993 biocompatibility testing, analytical testing, interventional, surgical, toxicology, pharmacology, pain, physician training, bioskills, animal model development, and complete pathology services, you’ll be able to develop and conduct a powerful preclinical program.

Whether your company is a startup or an established industry leader, our experienced scientific staff has the expertise to meet your research needs and timelines. Pilot and screening evaluations, feasibility and efficacy testing or ultimately GLP safety studies of the finished product, you will have industry experts to rely on every step of the way.

We strive to deliver comprehensive, yet rapid service with the understanding that in product development, the only constant is change. We’ve tailored our processes, capacity, and customer service to keep up with today’s fast paced business cycles. APS will go from a quote to a ready to implement study design with your time lines in full focus.

Challenge us -- we will meet your challenge

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