/EINPresswire.com/ -- TORONTO, ON--(Marketwired - May 15, 2017) - During a live broadcast, industry expert and CEO of ClinDisc s.r.o., Dmitriy Gorichev will outline the benefits of an active eTMF system, along with a review of how the upcoming European Medicines Agency (EMA) regulations can affect your eTMF workflows.

There is no "silver bullet" tool to help you ensure the quality of a clinical trial but selecting a proper electronic trial master file (eTMF) solution is one of the keys to success. Many companies use homegrown systems as eTMF solutions, but those lack some vital functionalities to cover the complete TMF Workflow process. Additionally, they might not be user-friendly and sometimes they're more complex than necessary. Moreover, when it comes to data archiving it can become very challenging and time consuming to ensure that the structure of the data and all metadata are properly preserved for many years of storage.

Improper organization of TMF workflows can be a waste of resources for a company, and can put it at a greater risk of non-compliance. Nobody can argue that eTMF data quality can be a big issue. However, by having properly organized processes with a system which can facilitate them, eTMF data quality can become your strong point.

In this webinar, we will be covering various aspects of proper organization of eTMF workflow including:

• How to achieve a balance between rich functionality of a professional eTMF solution and a user-friendly system
• How to make eTMF active, reminding users about missing documents
• Making the right files available with just a few clicks

The speaker will also discuss the Quality Checks and DIA TMF Reference Model and how to make sure the right documents are filed correctly. An outline of how you can do this in a timely manner without employing extra staff to do the filing and verification, to make sure you are always audit ready will be reviewed.

Join Dmitriy Gorichev on Monday, June 5, 2017 at 11am EDT (4pm BST). For more information or to register for this complimentary event, visit: eTMF Workflows: Active eTMF to Improve the Quality of Clinical Trials

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global Life Sciences community. Every year thousands of industry practitioners (from pharmaceutical & biotech companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.

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