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WATCH
The benefit of Going with a Small CRO as your Development Partner
WATCHLost in Translation - How to Get Clinical Operations and Data Management to Speak the Same Language
Presented at Medidata NEXT 2022 in New York City.WATCHExploring the Impact of Decentralized Clinical Trials
As a full-service CRO at the heart of drug development, PROMETRIKA has witnessed the increasingly rapid shift toward remote medicine and the impact this has on clinical trials. On the leading end of this spectrum is the push toward de-centralized…WATCHAchieving Effective Outsourcing Strategy that Truly Supports Development Goals for Emerging Biotechs
PROMETRIKA’s Chelsey Ryan, Associate Director of Clinical Operations and Pharmacovigilance, speaks at the Chief Medical Officer Summit 360°WATCHPractical Operational and Data Collection Challenges
WATCHData Certainty in Times of COVID-19 and Beyond: from eSource to Submission
Chelsey Ryan, Senior Clinical Trial Manager, PROMETRIKA, LLC joined this MassBio panel discussion on the imperative that clinical trial sponsors embrace technical innovation to meet the demands of today’s world. This forum focused on how tools such…WATCHThe Era of Flexible Monitoring: Centralized Data Review and TSDV
The benefit of Going with a Small CRO as your Development Partner
Lost in Translation - How to Get Clinical Operations and Data Management to Speak the Same Language
Presented at Medidata NEXT 2022 in New York City.
Exploring the Impact of Decentralized Clinical Trials
As a full-service CRO at the heart of drug development, PROMETRIKA has witnessed the increasingly rapid shift toward remote medicine and the impact this has on clinical trials. On the leading end of this spectrum is the push toward de-centralized clinical trials (DCT) that promises many benefits in costs, patient inclusion, and execution of clinical trials.
Achieving Effective Outsourcing Strategy that Truly Supports Development Goals for Emerging Biotechs
PROMETRIKA’s Chelsey Ryan, Associate Director of Clinical Operations and Pharmacovigilance, speaks at the Chief Medical Officer Summit 360°
Practical Operational and Data Collection Challenges
Data Certainty in Times of COVID-19 and Beyond: from eSource to Submission
Chelsey Ryan, Senior Clinical Trial Manager, PROMETRIKA, LLC joined this MassBio panel discussion on the imperative that clinical trial sponsors embrace technical innovation to meet the demands of today’s world. This forum focused on how tools such as eSource and Direct Data Capture help trialists make confident, informed decisions, ensuring certainty of data from initial collection to regulatory submission.
The Era of Flexible Monitoring: Centralized Data Review and TSDV
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WATCH
PROMETRIKA - Rescue Studies - Ensuring a Smooth Transition - NO Q&A
WATCHLost in Translation - How to Get Clinical Operations and Data Management to Speak the Same Language
Presented at Medidata NEXT 2022 in New York City.WATCHPractical Operational and Data Collection Challenges
WATCHMigration of Rave Coder
PROMETRIKA Data Management and Database Programming successfully implemented Rave Coder on an existing study in Rave following the decommissioned of dsNavigator. Synonym lists were created and tested in the PROMETRIKA sandbox before Coder was…WATCHePRO Data Integration with Rave
PROMETRIKA LLC was one of the first Medidata CRO partners to become accredited in the Patient Cloud platform. In this presentation, you will hear about the usage of a fully integrated ePRO solution with Rave and Patient Cloud.WATCHStudy Conduct Medical Coding
In this session, Cathy Hult, Senior Manager, PROMETRIKA, LLC presents PROMETRIKA’s recent experience implementing the Medidata coder after many years of using an external, standalone, coding tool.WATCHUpgrade to RaveX - It's Worth It!
RaveX cloud-based EDC software is improved! We discuss the differences between Rave and RaveX, including new EDC User Interface updates, changes in Navigation within RaveX, updates to Task Management, changes to the subject home page, and…WATCHNEXT NYC l October 2018 l Breakout Session l Why Rave EDC?
Presented by … Amanda Rychel, PhD … Senior Project Manager, PROMETRIKA, LLC … RaveX is the latest version of Medidata’s popular EDC solution for collecting clinical trial data. Its predecessor, “classic” Rave, has been in use in the industry since…WATCHPROMETRIKA Discovers the Power of a Unified Platform
Hear from PROMETRIKA on their unified platform approach to data collection across complex trials.PROMETRIKA - Rescue Studies - Ensuring a Smooth Transition - NO Q&A
Lost in Translation - How to Get Clinical Operations and Data Management to Speak the Same Language
Presented at Medidata NEXT 2022 in New York City.
Practical Operational and Data Collection Challenges
Migration of Rave Coder
PROMETRIKA Data Management and Database Programming successfully implemented Rave Coder on an existing study in Rave following the decommissioned of dsNavigator. Synonym lists were created and tested in the PROMETRIKA sandbox before Coder was implemented. Synonym lists for Medical History, Concomitant Medications, and Adverse Events were programmatically generated from the last dsNavigator export file. PROMETRIKA successfully completed the multiple steps to ensure Coder could seamlessly continue activities in an ongoing study.
ePRO Data Integration with Rave
PROMETRIKA LLC was one of the first Medidata CRO partners to become accredited in the Patient Cloud platform. In this presentation, you will hear about the usage of a fully integrated ePRO solution with Rave and Patient Cloud.
Study Conduct Medical Coding
In this session, Cathy Hult, Senior Manager, PROMETRIKA, LLC presents PROMETRIKA’s recent experience implementing the Medidata coder after many years of using an external, standalone, coding tool.
Upgrade to RaveX - It's Worth It!
RaveX cloud-based EDC software is improved! We discuss the differences between Rave and RaveX, including new EDC User Interface updates, changes in Navigation within RaveX, updates to Task Management, changes to the subject home page, and improvements that allow quicker data entry. We create a subject in RaveX, enter and edit data, perform tasks on log forms, and review features that are no longer supported, why they are not supported, what will replace them and the planned availability of these features.
NEXT NYC l October 2018 l Breakout Session l Why Rave EDC?
Presented by
Amanda Rychel, PhD
Senior Project Manager, PROMETRIKA, LLCRaveX is the latest version of Medidata’s popular EDC solution for collecting clinical trial data. Its predecessor, “classic” Rave, has been in use in the industry since 2001. PROMETRIKA has successfully navigated the waters of this new Rave user interface (UI) and its Cloud Administration component. There are a number of advantages to adopting these newer products in your organization. Watch the video and learn how.
PROMETRIKA Discovers the Power of a Unified Platform
Hear from PROMETRIKA on their unified platform approach to data collection across complex trials.
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WATCH
Migration of Rave Coder
PROMETRIKA Data Management and Database Programming successfully implemented Rave Coder on an existing study in Rave following the decommissioned of dsNavigator. Synonym lists were created and tested in the PROMETRIKA sandbox before Coder was…WATCHData Certainty in Times of COVID-19 and Beyond: from eSource to Submission
Chelsey Ryan, Senior Clinical Trial Manager, PROMETRIKA, LLC joined this MassBio panel discussion on the imperative that clinical trial sponsors embrace technical innovation to meet the demands of today’s world. This forum focused on how tools such…WATCHePRO Data Integration with Rave
PROMETRIKA LLC was one of the first Medidata CRO partners to become accredited in the Patient Cloud platform. In this presentation, you will hear about the usage of a fully integrated ePRO solution with Rave and Patient Cloud.WATCHThe Era of Flexible Monitoring: Centralized Data Review and TSDV
WATCHStudy Conduct Medical Coding
In this session, Cathy Hult, Senior Manager, PROMETRIKA, LLC presents PROMETRIKA’s recent experience implementing the Medidata coder after many years of using an external, standalone, coding tool.WATCHUpgrade to RaveX - It's Worth It!
RaveX cloud-based EDC software is improved! We discuss the differences between Rave and RaveX, including new EDC User Interface updates, changes in Navigation within RaveX, updates to Task Management, changes to the subject home page, and…WATCHNEXT NYC l October 2018 l Breakout Session l Why Rave EDC?
Presented by … Amanda Rychel, PhD … Senior Project Manager, PROMETRIKA, LLC … RaveX is the latest version of Medidata’s popular EDC solution for collecting clinical trial data. Its predecessor, “classic” Rave, has been in use in the industry since…WATCHPROMETRIKA Discovers the Power of a Unified Platform
Hear from PROMETRIKA on their unified platform approach to data collection across complex trials.Migration of Rave Coder
PROMETRIKA Data Management and Database Programming successfully implemented Rave Coder on an existing study in Rave following the decommissioned of dsNavigator. Synonym lists were created and tested in the PROMETRIKA sandbox before Coder was implemented. Synonym lists for Medical History, Concomitant Medications, and Adverse Events were programmatically generated from the last dsNavigator export file. PROMETRIKA successfully completed the multiple steps to ensure Coder could seamlessly continue activities in an ongoing study.
Data Certainty in Times of COVID-19 and Beyond: from eSource to Submission
Chelsey Ryan, Senior Clinical Trial Manager, PROMETRIKA, LLC joined this MassBio panel discussion on the imperative that clinical trial sponsors embrace technical innovation to meet the demands of today’s world. This forum focused on how tools such as eSource and Direct Data Capture help trialists make confident, informed decisions, ensuring certainty of data from initial collection to regulatory submission.
ePRO Data Integration with Rave
PROMETRIKA LLC was one of the first Medidata CRO partners to become accredited in the Patient Cloud platform. In this presentation, you will hear about the usage of a fully integrated ePRO solution with Rave and Patient Cloud.
The Era of Flexible Monitoring: Centralized Data Review and TSDV
Study Conduct Medical Coding
In this session, Cathy Hult, Senior Manager, PROMETRIKA, LLC presents PROMETRIKA’s recent experience implementing the Medidata coder after many years of using an external, standalone, coding tool.
Upgrade to RaveX - It's Worth It!
RaveX cloud-based EDC software is improved! We discuss the differences between Rave and RaveX, including new EDC User Interface updates, changes in Navigation within RaveX, updates to Task Management, changes to the subject home page, and improvements that allow quicker data entry. We create a subject in RaveX, enter and edit data, perform tasks on log forms, and review features that are no longer supported, why they are not supported, what will replace them and the planned availability of these features.
NEXT NYC l October 2018 l Breakout Session l Why Rave EDC?
Presented by
Amanda Rychel, PhD
Senior Project Manager, PROMETRIKA, LLCRaveX is the latest version of Medidata’s popular EDC solution for collecting clinical trial data. Its predecessor, “classic” Rave, has been in use in the industry since 2001. PROMETRIKA has successfully navigated the waters of this new Rave user interface (UI) and its Cloud Administration component. There are a number of advantages to adopting these newer products in your organization. Watch the video and learn how.
PROMETRIKA Discovers the Power of a Unified Platform
Hear from PROMETRIKA on their unified platform approach to data collection across complex trials.
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WATCH
PROMETRIKA - An Unusual Case Study of Mapping Data Into The SDTM DA (Drug Accountability) Domain
WATCHApplying Agile Methodology to Statistical Programming
WATCHOptimizing TLF Generation: Titles and Footnotes-Applying a New Idea to a Basic Approach
WATCHKeys to a Successful Natural History Study: A Statistical Challenge At Its Core
Webinar Series: Keys to a Successful Natural History Study: A Statistical Challenge At Its Core.WATCHKeys to a Successful Natural History Study: Forging Successful Sponsor-Academia Collaborations in the Real World
In this first presentation of a 3-part webinar series, hear about the challenges of designing a successful natural history study and the unique opportunities to partner with academic or non-profit organizations.WATCHSurvey of Statistical Study Design and Analysis Methods for Rare Disease Development Programs
Miganush Stepanians, PhD, PROMETRIKA’s President and CEO provides an overview of the challenges of rare disease development programs and the statistical study design and analysis methods used.PROMETRIKA - An Unusual Case Study of Mapping Data Into The SDTM DA (Drug Accountability) Domain
Applying Agile Methodology to Statistical Programming
Optimizing TLF Generation: Titles and Footnotes-Applying a New Idea to a Basic Approach
Keys to a Successful Natural History Study: A Statistical Challenge At Its Core
Webinar Series: Keys to a Successful Natural History Study: A Statistical Challenge At Its Core.
Keys to a Successful Natural History Study: Forging Successful Sponsor-Academia Collaborations in the Real World
In this first presentation of a 3-part webinar series, hear about the challenges of designing a successful natural history study and the unique opportunities to partner with academic or non-profit organizations.
Survey of Statistical Study Design and Analysis Methods for Rare Disease Development Programs
Miganush Stepanians, PhD, PROMETRIKA’s President and CEO provides an overview of the challenges of rare disease development programs and the statistical study design and analysis methods used.
FEATURED VIDEO
PROMETRIKA - 20 Years of Quality, Integrity, and Innovation!
Over the past 20 years, not only have we helped our clients bring life-changing drugs to market, we have also become key thought leaders in the industry.