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Main address: Margarethenstrasse 47 4053 Basel, Switzerland ,
Tel:+41 61 865 60 60 , E-mail: info(at)clinerion.com Website:

Clinerion Quality Risk Management System

Clinerion Quality Risk Management System

Cloud-based risk management system for controlling risks to clinical trial quality.

Clinerion Patient Recruitment System

Clinerion Patient Recruitment System

Optimized study design, precise site selection and faster patient recruitment for clinical research - in real time.



Webinars

Learn all about how Clinerion enhances the speed and efficiency of your clinical trials.



Webinar: Quality Risk Management in Clinical Trials and Pharmacovigilance

Date: January 19, 2017.
Time: 12:00 PM - 1:30 PM Eastern.

Webinar instructors: Randy Ramin-Wright, Head of Quality Risk Management and Klaudia Keller, Senior Quality Risk Analyst.

Registration: www.barnettinternational.com/Web-Seminars/Quality-Risk-Management-in-Clinical-Trials-and-Pharmacovigilance/

Description: The ICH Q9 Quality Risk Management (QRM) guideline has become an accepted standard, facilitating the development and implementation of a systematic risk-based approach to quality management of clinical trials and pharmacovigilance. Industry and regulatory bodies, including the EMA and FDA, have recognized the need and benefits of implementing a risk-based approach to quality management.

This web seminar is designed to provide a strong conceptual foundation of the principles of quality risk management with a clear focus on the application of these principles. We will address applying QRM to support decision-making throughout the clinical trial management and pharmacovigilance process, allocating limited resources effectively to areas of high risk, and preparing the participant to become an active contributor towards risk-based quality management at his/her organization.

Learning objectives:

  • Define Quality Management System (QMS) levels for applicable areas in clinical trials and pharmacovigilance.
  • Build quality at key points in the process.
  • Apply QRM principles: Identification and quantification of key risk indicators.
  • Implement a quality by design approach to overcome shortcomings in quality and compliance.
  • Leverage existing information to support decision-making in resource allocation within clinical trials.
  • Create a governance model to support mitigation strategies and the overall QMS infrastructure.


Webinar Series: Patient Recruitment for Clinical Trials Based on Hospital e-Records (Session III (Americas))

Date: September 21, 2016.

Webinar instructor: Randy Ramin-Wright, Clinerion Account Manager.

Registration: now closed.

Description:
Are you conducting clinical trials?
Do you want to attract international clinical trial sponsors?
Do you want to increase trial revenue and efficiency?

One of the biggest challenges in clinical research is identifying patients whose profiles match study protocols. Clinerion’s Patient Recruitment System is free for hospitals and supports patient search by querying hospital medical records. Our partner hospitals have higher visibility to international trial sponsors. At the same time, the amount of effort required to identify suitable patients is greatly reduced.

In the webinar we will demonstrate our easy-to-use Patient Recruitment System, highlighting how we make the clinical trials process at hospitals and pharmaceutical companies quicker and more efficient.

During the webinar, we will address frequently asked questions, such as those regarding patient privacy and data security. You will be able to add comments or ask questions.

This webinar addresses the following roles:

  • President / CEO / Superintendent / Hospital Manager
  • Head of Clinical Trial Unit
  • Chief Information Officer / IT Director
  • Commercial / Business Development Director
  • Executives responsible for clinical trials at pharmaceutical companies and CROs
     

We are looking forward to meeting you at the webinar!
The Clinerion Team



Webinar Series: Patient Recruitment for Clinical Trials Based on Hospital e-Records (Session II (Europe))

Date: September 20, 2016.

Webinar instructor: Dr. Tigran Arzumanov, Clinerion Head of Sales.

Registration: now closed.

Description:
Are you conducting clinical trials?
Do you want to attract international clinical trial sponsors?
Do you want to increase trial revenue and efficiency?

One of the biggest challenges in clinical research is identifying patients whose profiles match study protocols. Clinerion’s Patient Recruitment System is free for hospitals and supports patient search by querying hospital medical records. Our partner hospitals have higher visibility to international trial sponsors. At the same time, the amount of effort required to identify suitable patients is greatly reduced.

In the webinar we will demonstrate our easy-to-use Patient Recruitment System, highlighting how we make the clinical trials process at hospitals and pharmaceutical companies quicker and more efficient.

During the webinar, we will address frequently asked questions, such as those regarding patient privacy and data security. You will be able to add comments or ask questions.

This webinar addresses the following roles:

  • President / CEO / Superintendent / Hospital Manager
  • Head of Clinical Trial Unit
  • Chief Information Officer / IT Director
  • Commercial / Business Development Director
  • Executives responsible for clinical trials at pharmaceutical companies and CROs
     

We are looking forward to meeting you at the webinar!
The Clinerion Team



Webinar Series: Patient Recruitment for Clinical Trials Based on Hospital e-Records (Session I (Asia))

Date: September 6, 2016.

Webinar instructor: Dr. Tigran Arzumanov, Clinerion Head of Sales.

Registration: now closed.

Description:
Are you conducting clinical trials?
Do you want to attract international clinical trial sponsors?
Do you want to increase trial revenue and efficiency?

One of the biggest challenges in clinical research is identifying patients whose profiles match study protocols. Clinerion’s Patient Recruitment System is free for hospitals and supports patient search by querying hospital medical records. Our partner hospitals have higher visibility to international trial sponsors. At the same time, the amount of effort required to identify suitable patients is greatly reduced.

In the webinar we will demonstrate our easy-to-use Patient Recruitment System, highlighting how we make the clinical trials process at hospitals and pharmaceutical companies quicker and more efficient.

During the webinar, we will address frequently asked questions, such as those regarding patient privacy and data security. You will be able to add comments or ask questions.

This webinar addresses the following roles:

  • President / CEO / Superintendent / Hospital Manager
  • Head of Clinical Trial Unit
  • Chief Information Officer / IT Director
  • Commercial / Business Development Director
  • Executives responsible for clinical trials at pharmaceutical companies and CROs
     

We are looking forward to meeting you at the webinar!
The Clinerion Team



Webinar: EHR-Driven Patient Recruitment Has Arrived!

Date: May 24, 2016.
Webinar instructor: Randy Ramin-Wright, Head of Quality Risk Management

Description: Could the non-recruiting site be a thing of the past? We hope so! Join us for this webinar to explore ways of using Big Data to find your perfect patient and help solve the challenge of recruiting anonymous patients. Faster and more efficient recruitment mechanisms can lead to significantly more patients being enrolled. Experience how new patient recruitment technology can potentially identify 10 to 30 times more ‘real world’ patients than those found through manual screening in a matter of minutes instead of weeks or months. Let your data speak for itself and start attracting more studies today!

Learning Objectives:

  • Understand ways in which technology can help identify suitable clinical study candidates for given protocols faster and more efficiently, ultimately leading to more patients enrolled.
  • Appreciate why your site is more likely to be selected for a clinical trial.
  • Recognize how the operational efficiencies of your site can increase.
  • Consider why connecting your site to a clinical research site network opens up new opportunities and can lead to a wider range of clinical trials bringing innovative drugs to your patient community.


Webinar: Quality Risk Management in Clinical Trials and Pharmacovigilance

Date: April 7, 2016.
Webinar instructors: Randy Ramin-Wright, Head of Quality Risk Management and Klaudia Keller, Senior Quality Risk Analyst

Description: The ICH Q9 Quality Risk Management (QRM) guideline has become an accepted standard, facilitating the development and implementation of a systematic risk-based approach to quality management of clinical trials and pharmacovigilance. Industry and regulatory bodies, including the EMA and FDA, have recognized the need and benefits of implementing a risk-based approach to quality management.

This web seminar is designed to provide a strong conceptual foundation of the principles of quality risk management with a clear focus on the application of these principles. We will address applying QRM to support decision-making throughout the clinical trial management and pharmacovigilance process, allocating limited resources effectively to areas of high risk, and preparing the participant to become an active contributor towards risk-based quality management at his/her organization.

Learning objectives:

  • Define Quality Management System (QMS) levels for applicable areas in clinical trials and pharmacovigilance
  • Build quality at key points in the process
  • Apply QRM principles: Identification and quantification of key risk indicators
  • Implement a quality by design approach to overcome shortcomings in quality and compliance
  • Leverage existing information to support decision-making in resource allocation within clinical trials
  • Create a governance model to support mitigation strategies and the overall QMS infrastructure
     

Who should attend:

  • Clinical Research, Operations, and Development Professionals
  • Medical Affairs Personnel
  • Safety and Risk Management/Operations Personnel
  • Compliance, Regulatory Affairs, and Clinical Quality Assurance Personnel


Webinar: Risk Based Monitoring Application Demo - New Interface & Analytics

Date: January 27, 2016.
Webinar presenter: Randy Ramin-Wright, Head of Quality Risk Management

Description: We at Clinerion offer a cloud-based industry-hardened Quality Risk Management System that empowers both big and small clinical research organizations to execute Risk-based Study Oversight and Risk-based Monitoring.

We have released a brand new version of our Quality Risk Management System including a modern, user friendly interface providing enhanced risk data analytics.

Watch for yourself and see how you can use Clinerion's Risk Based Monitoring Application to identify and mitigate your clinical quality risks and thereby make risk based monitoring a reality at your organization!

If you did not have the opportunity to hear the webinar live, then feel free to download the presentation slides and watch the video recording of the webinar.

If you have further questions regarding the webinar topic, or if you are interested in piloting the Risk Based Study Oversight and Monitoring approach and technology, please contact our speaker:

Randy Ramin-Wright: Randy Ramin-Wright

Download Webinar Presentation Slides: Webinar RBM Demo PDF.
Watch Webinar Video Recording: 



Webinar: Are You Prepared for the New ICH GCP Addendum?

Date: October 20, 2015.

The ICH has decided to modernize its approach to GCP in order to keep pace with the scale and complexity of clinical trials and to ensure appropriate use of technology.

In this webinar Peter Schiemann previewed what modern GCP will contain and underscored its likely impact on the organization, gave advice on how to prepare for its arrival and Randy Ramin-Wright explained and demonstrated how Clinerion's risk-based study oversight technology, the Quality Risk Radar fulfills the demands of modern GCP which includes Risk Based Monitoring.

If you did not have the opportunity to hear the webinar live, then feel free to download the presentation slides and watch the video recording of the webinar.

If you have further questions regarding the webinar topic, or if you are interested in piloting the Risk Based Study Oversight and Monitoring approach and technology, please contact our Speakers:

Dr. Peter Schiemann: Dr. Peter Schiemann.
Randy Ramin-Wright: Randy Ramin-Wright.

Download Webinar Presentation Slides: ICH GCP Addendum PDF.
Watch Webinar Video Recording:

Webinars