MakroCare Exhibiting at Risk-Based Monitoring in Clinical Studies
MakroCare, an International Development and Commercialization services firm that is dedicated to support life sciences industry, will be exhibiting at Risk-Based Monitoring in Clinical Studies event.
- Newark, NJ (1888PressRelease) October 18, 2013 - Risk-Based Monitoring (RBM) in Clinical Studies will be held at Sonesta Hotel in Philadelphia, PA from 24th to 25th Oct 2013.
MakroCare, an International Development and Commercialization services firm that is dedicated to support life sciences industry, will be exhibiting at this event. Visitors/Delegates are welcome to our booth to know more about our company, services and capabilities in supporting implementation RBM.
This in-depth event on RBM will equip attendees with strategies to achieve high quality , tremendous time and cost savings in clinical trial management. The emerging practices being pushed by the FDA and industry initiatives are trending to reduce SDV and improve quality, efficiencies by implementing a risk-based approach to monitoring.
Beyond Theory - Proven Strategies to Implement and Standardize Approaches for High-Quality, Risk-Based Monitoring:
1) Gain critical updates directly from a panel of TransCelerate members on their initiative to create industry standards
2) Achieve time and cost savings by reducing source data verification (SDV) through a risk-based approach
3) Hear directly from the FDA about its draft guidance and expectations for documentation and monitoring
4) Gain insight from industry leaders through case studies that employ various risk-based approaches
5) Identify technology advancements that effectively reduce and streamline SDV
6) Answer the burning question - How much is enough?
Who Should Attend:
Executive, Senior-level director or manager within the pharmaceutical, biotech or CRO industries with responsibilities or involvement in the following areas: Clinical Operations, Clinical Compliance, Study Monitoring, Clinical Quality, Clinical Research, Data Management, EDC Operations, Quality Assurance, Regulatory Affairs, Study Management, This conference will also benefit EDC and clinical monitoring service vendors, as well as clinical and quality risk consultants.
###
space
space
Satisfied Users & 
Approved Press Releases
Print
Email
Report Spam