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ClinCapture® Demo
Live demo of ClinCapture, Clinovo's open source electronic data capture (EDC) system
The development of open source technology in the clinical arena has been rapidly growing, explained top-tier panelists from leading pharmaceutical, biotechnology, and medical device companies at a Silicon Valley BioTalks. They described how open source technologies save time, improve re-usability and simplify the customization of systems to a company's needs.
This webinar will demonstrate how open source technology presents an innovative solution to the current challenging climate, and will include a demo of ClinCapture, Clinovo's open source clinical trial system for Electronic Data Capture. Our open source EDC experts validated and enhanced the #1 open source platform that leverages over 11,000 users and developers.
CDISC® Express Demo
Live demo of CDISC Express®, our free CDISC® SDTM mapping tool
The mission of CDISC is to develop and support global, platform-independent data standards to improve medical research. As a CDISC® Gold Member, Clinovo has been continuously supporting the adoption of CDISC® standards to accelerate clinical trials. This webinar benefits industry professionals looking for efficient ways to convert clinical data to global standards.
Speaker: Ale Gicqueau, CEO and President at Clinovo
Medidata Rave® Custom Functions
Implementing the Rave Custom Functions Best Suited to your Clinical Study Requirements
Configuring a clinical EDC study in Medidata Rave is simple with good training. Study builders can easily configure eCRFs and review complex edit checks and derivations. However, they often face limitations in Rave when using edit checks and derivations. As we will demonstrate in our webinar, custom functions are better adapted to address complex study protocol requirements. Our Medidata Rave experts will discuss key benefits and programming techniques to implement the custom functions best-suited to your clinical study requirements.
Speakers: Pascal Royet, VP of Business Operations at Clinovo, and Venkat Sungishala, Sr. Manager of EDC at Clinovo
Open Source Technologies for Clinical Trials #1
Eric Morrie, Manager for Clinical Programming at Abbott Vascular, shares his expertise in open source systems for clinical trials
Open source is becoming more and more prevalent in clinical trials, introducing an innovative way to save costs while keeping high clinical data quality and security. With over 10,000 users, clinical open source EDC systems are a strong example of the tremendous value clinical open source software can bring to the clinical trial process of pharmaceutical, biotechnology and medical device companies. Open source technologies are used for Business Intelligence, CDISC®, cancer research etc. What systems are used in the industry? What are the key benefits of open source technologies for sponsors? What are the best practices for a successful implementation of clinical open source softwares?
Speakers: Eric Morrie, Clinical Programming Manager at Abbott Vascular and Marc Desgrousilliers, Chief Technology Officer at Clinovo
Implementing Adaptive Clinical Trials
Best practices to successfully plan for an adaptive clinical trial
With the ever rising cost and complexity of clinical trials, adaptive design is a promising solution highly regarded by both pharmaceutical companies and regulatory agencies. It promotes cost reduction whilst improving overall efficiency. By allowing pre-planned modifications in studies, adaptive trials allow higher flexibility with shorter timelines and, ultimately, better chances of success.
What are the different types of adaptive clinical trials? What are the main advantages of this method and the main risks? What are the best practices to implement and conduct successful adaptive trials using existing EDC tools?
Speakers: Peter Shabe, President of Advance Research Associates and Pascal Royet, VP of Business Operations at Clinovo
Open Source Technologies for Clinical Trials #2
Mark Burns, Clinical Data Specialist at Intuitive Surgical, shares his expertise in open source systems for clinical trials
We continue our series of webinar of open source technologies for clinical trials. Our keynote speaker for this second webinar is Mark Burns, Clinical Data Specialist at Intuitive Surgical.
Open source is becoming more and more prevalent in clinical trials, introducing an innovative way to save costs while keeping high clinical data quality and security. With over 10,000 users, clinical open source EDC systems are a strong example of the tremendous value clinical open source software can bring to the clinical trial process of pharmaceutical, biotechnology and medical device companies. Open source technologies are used for Business Intelligence, CDISC, cancer research etc. What systems are used in the industry? What are the key benefits of open source technologies for sponsors? What are the best practices for a successful implementation of clinical open source softwares?
Speakers: Mark Burns, Clinical Data Specialist at Intuitive Surgical, and Marc Desgrousilliers, VP of Technical Operations at Clinovo
CRO Governance Model for Emerging & Virtual Biopharma
Implementing effective organizational strategies to manage the CRO-sponsor relationship
Regulatory requirements have significantly lengthened and complicated clinical trials, resulting in an 11% annual rise in clinical testing expenses and delays in FDA submission. To avoid these rising clinical testing expenses, biotechnology companies outsource their clinical trial management to Contract Research Organizations (CROs). Because of its scale and cost advantage, the virtual company model has been attracting more and more companies. However, operating virtually represents challenges to both biotech companies and CROs. This webinar benefits executives looking for organizational strategies that optimize their relationships with sponsor companies, in order to achieve positive clinical trial endpoints.
Speaker: Matthew Smith, VP of Business Operations at Clinovo