Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina)
$1799
Category: Pharma Webinars | Date: January 19, 2012, 2:00 pm GMT
Course Description This two-day comprehensive Course on Latin America Regulatory compliance requirements will cover topics ranging from pre-clinical and clinical requirements through product regis...
Understanding and Implementing the Medical Device Directive
$1799
Category: Pharma Webinars | Date: January 26, 2012, 2:00 pm GMT
Most medical devices marketed in the European Union must follow the Medical Device Directive (MDD); IVD device and active implantable devices have other directives. The MDD can be complicated, especia...
Pharmaceutical Hazard Categorization and Control
Free
Category: Pharma Webinars | Date: January 11, 2012, 6:00 pm GMT
Xcelience is delighted to present a free webinar from their "Scentific Seminar Series." These webinars engage the pharmaceutical community about the challenges of drug development. This webinar,...
Clear as Mud: Obtaining & Marketing your 510(K) with Today’s FDA
$479
Category: Pharma Webinars | Date: January 27, 2012, 2:00 pm GMT
An interactive workshop to ensure you understand how to obtain a 510(k) in today's environment at FDA. Knowing how to get your application through FDA quickly can save millions of dollars in unnece...
The Ins and Outs of CTMS Data Migration
Free
Category: Pharma Webinars | Date: February 16, 2012, 3:00 pm GMT
You are considering implementing a new clinical trial management system (CTMS), or maybe you have already made the decision. But you are wondering: What should we do with the data in our legacy system...
Oracle Clinical / Remote Data Capture Implementation Standards and Best Practices
Free
Category: Pharma Webinars | Date: February 2, 2012, 3:00 pm GMT
As your organization implements or upgrades to a newer version of Oracle Clinical (OC) and Remote Data Capture (RDC), there are many considerations to take into account. Educating yourself on best pr...
How to Migrate Drug Safety and Pharmacovigilance Data Cost-Effectively and with Minimum Risk
Free
Category: Pharma Webinars | Date: January 25, 2012, 3:00 pm GMT
With the advancement of technology and the high cost of maintaining legacy safety and pharmacovigilance systems, organizations are forced to migrate to the latest technologies such as Argus Safety, th...
Open Source Technologies for Clinical Trials
Free
Category: Pharma Webinars, Technology Webinars | Date: November 17, 2011, 5:00 pm GMT
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,...
Implementing Adaptive Clinical Trials
Free
Category: Pharma Webinars | Date: November 16, 2011, 5:00 pm GMT
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 enables to reduce unne...
Navigating Pediatric Regulations in the United States and European Union
Free
Category: Health Webinars, Pharma Webinars | Date: November 8, 2010, 4:00 pm GMT
The FDA and EMA's requirement of pediatric plans for new active ingredients, dosage forms, dosing regimens or routes of administration has made a thorough understanding of such regulations essential. ...
Success Strategies in Life Sciences Industry
Free
Category: Pharma Webinars | Date: November 4, 2011, 7:00 am GMT
The life sciences industry faces many challenges, such as patent protection, increasing cost of conducting research and development (R&D), drying of product pipeline and threat from generics. It i...
Reducing the Barriers to the Conduct and Oversight of Clinical Trials: A Case Study
Free
Category: Pharma Webinars | Date: October 18, 2011, 4:00 pm GMT
In a recent announcement of the proposed revisions to existing federal regulations governing human research subjects, the US Department of Health and Human Services (HHS) acknowledged, “There is ver...
CDISC® SDTM Conversion
Free
Category: Pharma Webinars | Date: October 26, 2011, 5:00 pm GMT
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...
Medidata Rave® Custom Functions
Free
Category: Pharma Webinars, Technology Webinars | Date: October 11, 2011, 5:00 pm GMT
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 limit...
Implementing Adaptive Clinical Trials
Free
Category: Pharma Webinars | Date: September 27, 2011, 5:00 pm GMT
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 enables to reduce unne...
Open Source Technologies for Clinical Trials
Free
Category: Pharma Webinars | Date: September 21, 2011, 5:00 pm GMT
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 ...
CRO Governance Model for Emerging & Virtual Biopharma
Free
Category: Pharma Webinars | Date: August 17, 2011, 5:00 pm GMT
Regulatory requirements have significantly lengthened and complicated clinical trials, resulting in an 11% annual rise in clinical testing expenses and delays in FDA submission. Because of their scale...
Searching the Scientific Literature More Effectively
Free
Category: Pharma Webinars | Date: August 24, 2011, 4:00 pm GMT
With thousands of articles being published weekly, there is no shortage of available information relevant to ones research. But how do you sift through so much information to find the experimental obs...
Open Source Technologies for Clinical Trials
Free
Category: Pharma Webinars | Date: August 25, 2011, 5:00 pm GMT
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 ...
CDISC® SDTM Conversion
Free
Category: Pharma Webinars | Date: August 18, 2011, 5:00 pm GMT
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...
Accelerate Your Research and Discovery
Free
Category: Pharma Webinars | Date: July 28, 2011, 3:00 pm GMT
The information space in which life scientists work is growing in complexity and volume, especially with the technological advances of next generation sequencing which have brought about an exponentia...
Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs By compliance2go
$189
Category: Pharma Webinars | Date: October 4, 2011, 6:00 pm GMT
Summary This Medical Device training will be discussing the newly-updated requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Directive and the European requirements...
Drug Master Files (DMFs) – Understanding and Meeting Your Global Regulatory and Processing Responsibilities
$189
Category: Pharma Webinars | Date: October 14, 2011, 6:00 pm GMT
Description : This DMFs (Drug Master Files) training will discuss the current review and enforcement climate within FDA and the manner in which drug master files (DMFs) are reviewed by FDA personnel. ...
Welcome to M and C Packaging India
Free
Category: Pharma Webinars | Date: July 21, 2011, 9:00 am GMT
We are attempting here to make you aware of the benefits that other organizations like yours have realized from working with M&C Packaging. It would be our pleasure to demonstrate our capabilities...
Implementing the Rave Custom Functions Best Suited to your Clinical Study Requirements
Free
Category: Pharma Webinars | Date: July 20, 2011, 5:00 pm GMT
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 limit...
CDISC Express Demo
Free
Category: Pharma Webinars | Date: July 28, 2011, 5:00 pm GMT
Discover CDISC® Express, our free innovative SDTM mapping tool. CDISC Express is a free SAS application that automatically converts clinical data into CDISC SDTM using an Excel framework. CDISC E...
Open Source Technologies for Clinical Trials
Free
Category: Pharma Webinars | Date: July 19, 2011, 5:00 pm GMT
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,...
Flexible Study Design in Oracle Clinical and Remote Data Capture 4.6
Free
Category: Pharma Webinars | Date: August 25, 2011, 3:00 pm GMT
Oracle Clinical (OC) / Remote Data Capture (RDC) 4.6 provides the ability to conduct global clinical trials more efficiently and effectively. The newest release features significant enhancements that ...
Using Siebel Clinical for Your Specific Job Function
Free
Category: Pharma Webinars | Date: September 22, 2011, 3:00 pm GMT
Siebel Clinical is well-known as a robust clinical trial management system (CTMS) that streamlines clinical trial management. The system can be operated uniquely by users in various roles at sponsor a...
Top 10 Reasons Why You Need a Clinical Trial Management System
Free
Category: Pharma Webinars | Date: August 23, 2010, 3:00 pm GMT
Trying to build a business case for a clinical trial management system (CTMS) at your organization? Let us help you! BioPharm Systems’ Clinical Trial Management Solutions practice has decades of exp...
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A while back we have launched the Request a webinar feature, so that our visitors can tell us what they are interested in. To all webinar hosts out there, here ...
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