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Pharmaceutical Research Software

16 software items found

MonolixSuite™ - Pharmacometric Analysis Software

MonolixSuite™ - Pharmacometric Analysis Software

by:Simulations Plus   based inLancaster, CALIFORNIA (USA)
Modules like PKanalix® support compartmental and non-compartmental analyses, while Simulx® excels in clinical trial simulations, enhancing decision-making in drug development. MonolixSuite aims to streamline complex analyses, making it a valuable asset for pharmaceutical researchers and ...
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Stability - ASAPprime

Stability - ASAPprime

by:FreeThink Technologies Inc.   based inMontvale, NEW JERSEY (USA)
The ASAPprime software is the only commercially-available software that enables pharmaceutical scientists to quickly and accurately determine drug substance and drug product shelf-life based on the Accelerated Stability Assessment Program (ASAP). This state-of-the-art, statistical software allows prediction of small-molecule drug product use periods, shelf-lives and drug substance retest periods ...
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EvidNet - Version EVIX-EXPLO - Graphic User Interface(GUI) based Exploratory Data Analysis (EDA) Tool

EvidNet - Version EVIX-EXPLO - Graphic User Interface(GUI) based Exploratory Data Analysis (EDA) Tool

by:EvidNet Inc.   based inSeongnam-si, SOUTH KOREA
EVIX-EXPLO™ is a graphic user interface(GUI)-based exploratory data analysis (EDA) tool. Using EVIX-EXPLO™, anyone can perform data analytic without the need for coding. Conduct end to end analyses from dataset creation to viewing analysis results in a web ...
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Provantis - Integrated Preclinical Windows-Based Software

Provantis - Integrated Preclinical Windows-Based Software

by:Instem Group   based inStone, UNITED KINGDOM
Provantis is a modern, fully integrated Windows-based system for organizations and universities engaged in non-clinical evaluation studies. From single-user Pathologists to full-function global Toxicology/Pathology laboratories, Provantis streamlines processes and workflows with straightforward, intuitive functionality for simple and complex studies within a GLP or non-GLP ...
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Proprietary Software for Development Division

Proprietary Software for Development Division

by:InterX   based inBerkeley, CALIFORNIA (USA)
InterX Development Division focuses on bridging the risk gap in Drug Discovery from drug targets to novel candidates. The Development Division applies InterX’s proprietary computer-aided drug design platform, while developing collaborations with Research Centers, Pharma companies, Start-ups, Academia and Accelerators. Such collaborations help distill the drug discovery process – from ...
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Novatek - Automated Proofreader and Proof Reading Software

Novatek - Automated Proofreader and Proof Reading Software

by:Novatek International   based inMontreal, QUEBEC (CANADA)
All healthcare and life science organizations that develop and manufacture products rely greatly on accurate informative text and printed labels to communicate to their end user and build their product brands successfully. Novatek’s software provides effective proof reading results to support the industry’s highest standards; eliminating printing errors in all product information ...
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NOTOCORD-hem - Software Platform for Acquisition, Display and Analysis

NOTOCORD-hem - Software Platform for Acquisition, Display and Analysis

by:Instem Group   based inStone, UNITED KINGDOM
NOTOCORD-hem™, developed by NOTOCORD, and now part the Instem solutions portfolio is the leading software platform for the acquisition, display and analysis of physiological signals, with a focus on the areas of Cardiovascular, Respiratory and Nervous System Research. NOTOCORD-hem is used by pharmaceutical companies, contract research ...
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QEdge - Full Product Quality (PQR)

QEdge - Full Product Quality (PQR)

by:Sarjen Systems Pvt. Ltd.   based inAhmedabad, INDIA
Pharmaceutical companies are required to submit a full Product Quality Review (PQR) or APQR in the U.S. and PQR in Europe to government health authorities annually, detailing key aspects of the manufacturing process for each drug they produce. APQR or PQR is a mandatory requirement that used to verify the consistency and appropriateness of an existing manufacturing process. It plays a critical ...
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Medidata - AI Integrated Evidence

Medidata - AI Integrated Evidence

by:Medidata   based inNew York, NEW YORK (USA)
Medidata AI Integrated Evidence connects historical data from more than 23,000 cross-sponsor clinical trials and 7 million patient volunteers with real world data to deliver powerful insights and the necessary evidence clinical development leaders need to increase the probability of trial success. Artificial intelligence and data can help fuel new ways of working on clinical trials and beyond. ...
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Freyr Reports - Regulatory Services in Mexico, COFEPRIS Registration, Mexico Regulatory Partner

Freyr Reports - Regulatory Services in Mexico, COFEPRIS Registration, Mexico Regulatory Partner

by:Freyr Solutions   based inPrinceton, NEW JERSEY (USA)
Freyr is a leading, niche, full-service global Regulatory Solutions and Services Company supporting, Large, Medium and Small size global Life sciences companies, (Pharmaceutical | Medical Device| Consumer Healthcare | Cosmetics | Food and Food Supplements | Chemicals) in their entire Regulatory Intelligence value-chain. With regional offices in Europe, North America, MENA and APAC regions and ...
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Halo - Image Analysis Platform Software

Halo - Image Analysis Platform Software

by:Indica Labs Inc.   based inAlbuquerque, NEW MEXICO (USA)
With unmatched ease-of-use and scalability, powerful analytic capabilities, and the fastest processing speeds available for digital pathology, pharmaceutical, healthcare and research organizations worldwide are using HALO for high-throughput, quantitative tissue analysis in oncology, neuroscience, metabolism, toxicology and more. ...
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Medidata - AI Synthetic Control Arm (SCA)

Medidata - AI Synthetic Control Arm (SCA)

by:Medidata   based inNew York, NEW YORK (USA)
Medidata AI Synthetic Control Arm (SCA®) offers the only external control arm created with cross-industry historical clinical trial data from 25,000+ clinical trials and 7 million patients. SCA can enable scientific research, cut costs and accelerate timelines in scenarios where a control group is hard to recruit or retain, such as rare or imminently life-threatening diseases with inadequate ...
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Sapio - Histopathology LIMS Software

Sapio - Histopathology LIMS Software

by:Sapio Sciences   based inBaltimore, MARYLAND (USA)
With our LIMS configurable technology and workflow templates, projects are completed in a fraction of the time and cost of standard LIMS ...
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Ontosight Discover - AI-based Discovery Engine for Real-Time Insights

Ontosight Discover - AI-based Discovery Engine for Real-Time Insights

Manufactured by:Intelligence   based inEschborn, GERMANY
Ontosight® Discover – a one stop solution for all relevant information within the pharmaceutical industry. The AI and blockchain powered discovery engine connects trillions of data points to accelerate your drug discovery and research process. You get real-time data insights on a fingertip for empowered, inspired & faster decisions. Automate up to ...
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Paige - Novel Predictive and Prognostic Tissue-Based Biomarkers Software

Paige - Novel Predictive and Prognostic Tissue-Based Biomarkers Software

by:Paige AI, Inc.   based inNew York City, NEW YORK (USA)
Paige is pioneering novel predictive and prognostic tissue-based biomarkers from tissue. By combining leading technology with groundbreaking AI, Paige derives novel insights from images of routine hematoxylin and eosin (H&E) stained tissue to identify morphologic features and biomarkers with clinical utility. Using proprietary computational pathology with exclusive clinical data ...
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Novatek - Clinical Assay Management Software

Novatek - Clinical Assay Management Software

by:Novatek International   based inMontreal, QUEBEC (CANADA)
In clinical studies, assessing and managing risks, as well as establishing areas of uncertainty that contribute to risk, are critical to a company’s decision making processes. Many business units within pharmaceutical, biotechnology and clinical research organizations must comply with federal regulations concerning their processes and computerized systems. ...
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