The quality of data collected during a clinical trial is the single most important factor determining its success.
Effective Clinical Data Management (CDM) plays a critical role in unlocking the value of clinical trial data by ensuring that it is integrated, characterized and easily accessible.
In addition to improving clinical trial outcomes, CDM is also crucial for adhering to the increased focus regulatory bodies are placing on data quality.
However, the reality for most businesses is that clinical trial data is still siloed, lacking in standardization and subject to human error. With that in mind, Pharma IQ Live: Clinical Data Management Excellence 2022 will be focused on:
Improving data quality through quality assurance processes and controlled data entry
Ensuring compliance by building in the required data standards and guidelines
Enhancing efficiency through automated workflows and data uploads
Increase speed to market by ensuring the submissions to the relevant regulatory bodies meet the necessary standards, are complete and of the necessary quality
Click on any of the register buttons on this page. Enter your information and secure your place
Step 2: Confirmation Email
This will be dispatched upon registration and will contain information like how to login to your Pharma IQ account - be sure to check your access in plenty of time!
Step 3: Schedule Time
Mark the time in your calendar so you can be free of distractions to watch the presentations
Step 4: Watch the Event
Click the link in the confirmation email and prepare questions for our industry-leading speakers
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