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BASi

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West Lafayette, Indiana, US

About BASi

Founded: 1974 Type: Public Company Size: 51-200 employees

BASi® provides drug developers with superior scientific research and innovative analytical instrumentation, which saves time, saves money, and saves lives, to bring revolutionary new drugs to market quickly and safely.

Founded in 1974, Bioanalytical Systems, Inc. (BASi) is a publicly traded, global company... Show more »

BASi® provides drug developers with superior scientific research and innovative analytical instrumentation, which saves time, saves money, and saves lives, to bring revolutionary new drugs to market quickly and safely.

Founded in 1974, Bioanalytical Systems, Inc. (BASi) is a publicly traded, global company headquartered in West Lafayette, Indiana, that provides contract research services and sophisticated, niche instrumentation to the life sciences industry, primarily in drug research, discovery, and development in commercial and academic settings. BASi also provides critical testing services for biotech and the rapidly growing generic and biosimilars drug sectors.

For four decades, BASi has established itself as an industry leader in contract research and as a resource for instrumentation that meets the demanding requirements of today’s research labs. This can be attributed to an exceptional scientific team, originally established by company founder, Purdue University chemistry professor Peter Kissinger, and our leadership team, all of whom are results oriented and client focused. Indeed, the world’s leading pharmaceutical companies, academic centers, and myriad of startup companies in drug development and biotech count on BASi’s expertise in the demanding fields like electrochemistry and mass spectrometry; our unique capabilities in liquids, creams, patches and transdermals; and our unparalleled record with FDA audits to execute projects accurately, on schedule and on budget.

BASi instrumentation like the BASi Culex NxT™ automated sampling system can be found in labs around the world and is readily available through our dynamic online “store”. This dynamic portal provides customers with a wealth of information, access to experts, the ability to customize instrumentation for their lab, and a wide range of consumables. BASi has a second location near Evansville, Indiana, dedicated to meeting the requirements of the preclinical toxicology and veterinary markets via animal models.

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Our Services (91)


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Toxicology

Price on request

Studies: Pilot/lead optimization, Acute, Sub-chronic, Chronic
Species: Rodents, Canines, Nonhuman Primates, Swine/Minipigs, Rabbits, Guinea pigs
Routes of Administration: Oral (Gavage, Capsule/tablet), Parenteral (Intramuscular, Intraperitoneal, Intravenous, Subcutaneous, Sublingual, Dermal, Intradermal, Ocular, Intravaginal, Rectal, Intranasal)

Studies: Pilot/lead optimization, Acute, Sub-chronic, Chronic
Species: Rodents, Canines, Nonhuman Primates, Swine/Minipigs, Rabbits, Guinea pigs
Routes of Administration: Oral (Gavage, Capsule/tablet), Parenteral (Intramuscular, Intraperitoneal, Intravenous, Subcutaneous, Sublingual, Dermal, Intradermal, Ocular, Intravaginal, Rectal, Intranasal)

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In vivo PK/PD Studies

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Our in vivo automated sampling lab is one of the largest in the USA. We have stationed 48 automated sampling Culex systems for a quick turn-around of your PKPD data. Our goal is to provide you with studies that meet your unique information needs while minimizing the number of study animals.

Our in vivo automated sampling lab is one of the largest in the USA. We have stationed 48 automated sampling Culex systems for a quick turn-around of your PKPD data. Our goal is to provide you with studies that meet your unique information needs while minimizing the number of study animals.

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In vitro Bioavailability/Bioequivalence Studies

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BASi® has proven experience and expertise with the FDA guidance documents and regulations on In Vitro Bioequivalence studies. The group's pharmaceutical product testing expertise mixed with the corporation's knowledge of bioequivalence studies and regulations creates the perfect match for our In Vitro services. BASi leverages the... Show more »

BASi® has proven experience and expertise with the FDA guidance documents and regulations on In Vitro Bioequivalence studies. The group's pharmaceutical product testing expertise mixed with the corporation's knowledge of bioequivalence studies and regulations creates the perfect match for our In Vitro services. BASi leverages the FDA guidances and all applicable literature sources to develop a sound scientific, regulatory plan.

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DART Studies

Developmental and Reproductive Toxicology Studies
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LC-MS

Liquid Chromatography-Coupled Mass Spectrometry
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Assay Development

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Small Molecule Bioanalysis

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Large Molecule Bioanalysis

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Clinical Biomarkers

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Biomarker Analysis

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Dermal Toxicity Studies

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Liquid Chromatography (LC)

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Pharmacology & Toxicology

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Project Management

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Clinical Chemistry

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UV-VIS Spectroscopy

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Controlled Release Systems

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Process Consulting

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Storage

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Product Stability Testing

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Drug Discovery & Development

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R&D Services

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Quality Assurance

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In vivo Toxicity Testing

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Synthetic Chemistry

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Contract Services Directory

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In vivo Drug Efficacy Testing

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Preclinical Study Design

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Patient Recruitment

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Micro FT-IR Analysis

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Spectroscopy

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Laboratory Equipment Manufacturing

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Batch Release Testing

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Animal Model in vivo Analyses

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HPLC

High Performance Liquid Chromatography
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High Throughput Screening (HTS)

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GMP Auditing

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GLP Auditing

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Forced Degradation Studies

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Drug Discovery

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Solubility and Dissolution Testing

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Regulatory Affairs Services

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Contract Research

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Consulting

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Phase I Clinical Trials

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Clinical Sample Analysis

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Scientific Sourcing

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Formulation Services

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Gas Chromatography (GC)

Gas Chromatography
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Combinatorial Chemistry

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Fluorescence Spectroscopy

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Chemical Analysis

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Toxicity Animal Model

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Product Development, Testing, and Packaging

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Human Blood Collection Service

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Biomarker Discovery

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Biological Testing

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Bioanalytical Assays

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Bioanalytical Analysis LC/MS/MS

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Analytical Method Validation

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Analytical Method Development

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Analytical Chemistry Services

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Clinical Trials, Consulting, and Management

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Animal Models and Studies

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Accelerated Stability Testing

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Mass Spectrometry

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Human Biospecimen Collection

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Spectrophotometry

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In vitro ADME/DMPK Studies

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Imaging & Spectroscopy

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Chemistry and Materials

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Cells and Tissues

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Antibody/Antigen Detection Based Testing

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Physical Analysis Methods

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Manufacturing Services

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Bioanalysis

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Separation/Purification Services

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Strength Analysis

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Clinical Research

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Clinical Laboratory Services

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Hit Identification

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Biology

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Chromatography

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Biospecimens

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Liquid Chromatography Coupled Mass Spectrometry Methods

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ADME/DMPK Studies

Drug Metabolism and Pharmacokinetics
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Biomarkers

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Engineering and Fabrication

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Safety Pharmacology

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Product Quality Control

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Clinical Ancillary and Sample Services

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Dane Brankle

Market Analyst
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Stephanie Miller

Director, Client Services

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