Industry Provider Profiles Company Type Services
PHT Corporation is the world’s only fully dedicated ePRO (electronic patient reported outcomes) and PRO (patient reported outcomes) Systems provider, and the only company that covers every clinical research phase from exploratory to post market.
PHT offers biopharmaceutical, life sciences, medical device companies and their CROs a unique, patented and comprehensive solution for acquiring, managing and analyzing data collected directly from patients through all phases of clinical development. Hearing the voice of the patients in your trial - directly and without distortion - is more important than ever. PHT's ePRO solutions give sponsors a reliable way to listen by capturing trustworthy self-reported data and by making it instantly available for real-time review.
More than 115 biopharmaceutical companies in 500 plus trials have used PHT's ePRO System to easily collect high quality, regulatory-compliant clinical trial data. PHT's proven ePRO Systems including the LogPad®, NetPRO™ and versatile SitePad® deliver the voice of the patient without distortion in 97 languages from homes and sites in 67 countries. Patient experiences captured firsthand by PHT's ePRO System have been used successfully in at least 18 regulatory submissions and 16 approvals to date resulting in 14 PRO-based label claims for sponsors.
PHT also is the only ISO-certified ePRO provider, giving customers the added assurance of certified logistics and inventory management processes across countries, languages and cultures.
In 2011 new PHT technology advancements now enable sponsors and CROs to:
Collect patient data on smartphones and/or tablets
Monitor ePRO dashboards online or in transit
Connect online 24/7 to the world class PHT Support Center
Transfer and integrate patient data using the latest industry standards
Get training online, on demand and via the medium that best supports the individual’s learning style
For more information on PRO and ePRO innovations, review the interactive content and demonstrations at phtcorp.com. Follow #PHT_ePRO on Twitter.
PHT's LogPad System is the most trusted ePRO solution used in clinical trials around the world. The LogPad System is an end-to-end ePRO solution, from scientific consulting and diary design to real-time data access and study archiving, with a hosted central server and ongoing study support.
The LogPad improves data quality and reduces data variance, enabling sponsors to be confident in their PRO data. The LogPad boasts the most robust set of features and capabilities in the ePRO industry, providing sponsors with the most flexibility when designing their global ePRO trials.
The PHT SitePad Tablet continues to capture site-based questionnaires, patient reported data (PRO) and clinical trial survey data efficiently and easily. Clinicians prefer the touch-screen convenience. It is available with a 10” or 12” screen which is ample size to display each question and all available answers, to avoid scrolling bias.
PHT NetPRO collects patient and clinician data for clinical trials and post-marketing studies via the Internet. Like all other PHT modalities, PHT NetPRO data is immediately viewable by sites and sponsors via the PHT StudyWorks™ portal. PHT NetPRO is an economical method for collecting patient reported outcome data or post-marketing safety data from large populations, and may be used to submit PRO data to support a labeling claim.
StudyWorks is an online portal which provides real-time access to data collected using the LogPad System, SitePad or NetPRO. With standard and custom data summaries and reports, it enables site personnel to manage compliance and enrollment, while helping sponsors stay on top of their global trial at all times. StudyWorks includes three groundbreaking ePRO solutions: SmartReports ™ dashboards report on patient eligibility, enrollment and compliance front and center. SmartReports Mobile™ is the first ePRO smartphone application to track site and subject compliance data. And, customers get online support anytime, anywhere with the new Live Chat 24/7.
eSense enables researchers to collect and evaluate physiological patient measurements together with ePROs. Integrated Peak Expiratory Flow (PEF) Meters and Glucometers enable scientific researchers to collect precise objective physiological data in conjunction with subjective patient-reported outcomes. The PHT eSense ePRO System delivers high-quality, attributable data that is 21 CFR Part 11 compliant.
PHT published the first free tool for choosing ePRO modalities for clinical trial data collection and management. The tool makes it fast and easy to select optimal ePRO modality for collecting patient data during any clinical research phase. Dozens of clinical trial managers within major pharmaceutical companies have used the PHT ePRO Modality Tool successfully to determine the right ePRO modality for specific trial types and phases.
PHT ePRO Designer – Know Before the Trial Starts: ePRO Designer is PHT's proprietary and validated rapid design tool to facilitate development of reliable ePRO studies. It supports multiple languages and allows PHT engineers, partners and sponsors (through Technology Transfer) to develop their own ePRO solutions in-house.
Study Archive – High quality data is the reason you conduct trials. The PHT Study Archive is delivered to sponsors and sites on durable CD- and DVD-ROM media. In addition to all study XML source and metadata, the Archive includes all contextual data for recreation (if required) complete with signatures, audit trails and permissions. The PHT Archive exceeds strict FDA and EMA regulations for data retention and trial reconstruction.
Clinical Trial Success Program (TSP) – Managed from Startup to Closeout: Not only does a successful ePRO system have to be well-designed and technically sound, but it must also be managed expertly, supported fully, and delivered consistently to sites around the world. In order to achieve these goals, PHT has institutionalized the Trial Success Program as its best practice processes for clinical trial deployment and data management. Together with our ISO certified quality management system, TSP ensures repeatable and efficient success for every clinical trial from kickoff to closeout.
PHT Support Center – The PHT in-house, multilingual Study Support Center (SSC) is ready 24/7. The SSCs in Boston and Geneva are staffed exclusively with PHT Technical Analyst and Support Specialists trained in the details of every client study. In addition to this live, telephone support, Live Chat is available online and within the PHT StudyWorks® portal.
PHT Support Center – The PHT in-house, multilingual Study Support Center (SSC) is ready 24/7. The SSCs in Boston and Geneva are staffed exclusively with PHT Technical Analyst and Support Specialists trained in the details of every client study. In addition to this live, telephone support, Live Chat is available online and within the PHT StudyWorks® portal.
In-Depth Training - PHT insists that clinical trial training support Study Monitors, Clinical Investigators and Study Coordinators throughout the life of the trial. As a result, PHT provides a blended training model which includes; protocol-specific ePRO device training & site support documentation, e-learning for self study & re-training, and PHT telephone and online Support Center 24/7. PHT training is available throughout the trial which is essential for long studies and those with complex workflows.
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