Clinical Studies,CRA,Clinical Research,Clinical Tr 2011 - Live webinar on Managing high-enrolling sites: CRO’s perspective By Compliance2go
Date2011-12-09
Deadline2011-12-08
Venuetexas, USA - United States
Keywordshealthcare;medical devies;biotech
Topics/Call fo Papers
Managing high-enrolling sites: CRO’s perspective
Friday, December 09, 2011
Description
Why should you Attend:
In the mutli-site cinical studies, it is quite common that one or more sites in several coutnries become high enrollers. These sites require more attention and support from the clinical research team (CRA, PM, Regulatory, Medical Monitoirs). If the clinical study was organized and managed at theses sites as required by the protocol, REB, regulatory authorities and ICH/GCP - these sites generate large amounts of valid, verifiable data - which is so important for sponsors and for future patients. If however, amount of attention ans support to the high-enrolling sites is not adequate - these sites often deviate from the protocol, study guidelines and even ICG/GCP. In this presentation we will review most common errors made by the sites' staff, and the sponsor's representatives. We will also review successful strategies that allowed high enrolling sites become high quality standards sites and be able to pass various inspections and audits.
Discount: Get 15 % Discount as a early bird registrations. Use Promo code CGO15
Description of the topic:
Managing high enrolling sites - from a perspective of a lead CRA who has several years experience of managing high enrolling sites on different protocols.
Areas Covered in the Session:
- Definition of a high-enrolling site
- Types of high-enrolling sites
- Most common problems encountered at high enrolling sites
- Case review
- Strategies implemented to ensure the high enrolling sites remain compliant and involved
-Importance of properlty managing high enrolling sites.
Who will benefit:
Regulatory Associates
Site staff
CRAs
PMs
Medical Monitors.
About Speaker
Alex Aptovcov MD, MBA, Senior Clinical Research Consultant based in Ontario, Canada. Alex holds the degrees of Doctor of Medicine from the National Medical University, Kiev, Ukraine and Masters of Busines Administration, Victoria, British Columbia, Canada. Alex has more than fifteen years of clinical research experience - as sub-Investigator in Ukraine, Patient Recruitment Consultant in New York and as Clinical Research Consultant (Canada, USA). For the last five years, Alex has worked on complex studies with a number of high enrolling sites
Purchase formats: Live: $189.00 One Dial In - Unlimited attendance $249 Recorded: $289.00, CD: $349.00
For any assistance contact us at support-AT-compliance2go.com or call us at 877.782.4696
http://www.compliance2go.com/index.php?option=com_...
Friday, December 09, 2011
Description
Why should you Attend:
In the mutli-site cinical studies, it is quite common that one or more sites in several coutnries become high enrollers. These sites require more attention and support from the clinical research team (CRA, PM, Regulatory, Medical Monitoirs). If the clinical study was organized and managed at theses sites as required by the protocol, REB, regulatory authorities and ICH/GCP - these sites generate large amounts of valid, verifiable data - which is so important for sponsors and for future patients. If however, amount of attention ans support to the high-enrolling sites is not adequate - these sites often deviate from the protocol, study guidelines and even ICG/GCP. In this presentation we will review most common errors made by the sites' staff, and the sponsor's representatives. We will also review successful strategies that allowed high enrolling sites become high quality standards sites and be able to pass various inspections and audits.
Discount: Get 15 % Discount as a early bird registrations. Use Promo code CGO15
Description of the topic:
Managing high enrolling sites - from a perspective of a lead CRA who has several years experience of managing high enrolling sites on different protocols.
Areas Covered in the Session:
- Definition of a high-enrolling site
- Types of high-enrolling sites
- Most common problems encountered at high enrolling sites
- Case review
- Strategies implemented to ensure the high enrolling sites remain compliant and involved
-Importance of properlty managing high enrolling sites.
Who will benefit:
Regulatory Associates
Site staff
CRAs
PMs
Medical Monitors.
About Speaker
Alex Aptovcov MD, MBA, Senior Clinical Research Consultant based in Ontario, Canada. Alex holds the degrees of Doctor of Medicine from the National Medical University, Kiev, Ukraine and Masters of Busines Administration, Victoria, British Columbia, Canada. Alex has more than fifteen years of clinical research experience - as sub-Investigator in Ukraine, Patient Recruitment Consultant in New York and as Clinical Research Consultant (Canada, USA). For the last five years, Alex has worked on complex studies with a number of high enrolling sites
Purchase formats: Live: $189.00 One Dial In - Unlimited attendance $249 Recorded: $289.00, CD: $349.00
For any assistance contact us at support-AT-compliance2go.com or call us at 877.782.4696
http://www.compliance2go.com/index.php?option=com_...
Other CFPs
- Live webcast on HIPAA Security Compliance - How Risk Analysis simplifies priorities and ensures compliance BY Compliance2go
- Live webinar on Excel Spreadsheet Compliance with 21 CFR 11 by Compliance2go
- Few day to Register on Live webcast Utilizing a Risk-based Approach to Meet Sponsor Monitoring Obligations By Glenda Guest & Lee Truax-Bellows BY Compliance2go
- Few days to register Live Webcast on US, EU and Japan GMP Requirements: Practical ICH Area Differences, Healthcare Authority Inspection Focus By Compliance2go
- Few days to register On Live webinar The 510(k) Submission Process By Compliance2go
Last modified: 2011-11-30 05:50:56