home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
 
  HUM-MOLGEN -> Events -> Courses and Workshops  
 

Navigating Pediatric Trials from recruitment to successful on-time completion - Webinar by GlobalCompliancePanel

 
  September 22, 2010  
     
 


GlobalCompliancePanel, Online Training Webinar
2010-10-12


Areas Covered in the Session:

  • Compilation of various regulatory and guidance documents from the FDA and OHRP on the conduct of research involving children
  • Recent guidances on compliance and general considerations in the conduct of research on children
  • General Considerations for the Clinical Evaluation of Drugs in Infants and Children
  • Discuss Clinical Investigation of Medicinal Products in the Pediatric Population
  • Nonclinical Evaluation of Pediatric Drug Products

Who Will Benefit: This webinar will provide valuable assistance to all personnel in: Pharmaceutical, Biotechnology, CROs and Research Facilities Conducting Clinical Trials including:

  • Pediatric Affairs
  • Pediatric Strategy
  • Pediatrics
  • Clinical Research
  • Clinical Development
  • Clinical Operations
  • Clinical Affairs
  • Medical Affairs
  • Clinical Trial Management
 
 
Organized by: GlobalCompliancePanel
Invited Speakers: Sandy Soliman: - Sandy is currently the co-founder and Chief Clinical Officer of Research Alliance LLC.; a consulting firm focused on global clinical trial solutions, tools, and training to streamline drug development to market. The firm advises clinical research sites, pharmaceutical drug development, biotech, medical device, and contract support organizations. Sandy began her journey in Clinical Research over 13 years ago. Her experience spans key aspects in multiple therapeutic areas and phases of drug development in the roles of study coordinator, site monitor, clinical research project manager, and trainer. She has effectively provided clinical research education and customized training in areas of the clinical research process, the FDA regulations, GCP (Good Clinical Practice) and the International Conference of Harmonization (ICH) guidelines. Sandy has created company-wide SOPs for a variety of relevant processes related to clinical research including, but not limited to, Informed Consent Process, Scheduling, Follow-up, Adverse Effect Reporting, etc. She has also been pivotal in coordinating, arranging, and managing the infrastructure of the company policies and procedures. She has also been awarded the National Association of Women Business Owners – NYC Chapter Phoenix Award 2008 and the National Association of Women Business Owners – NYC Chapter Golden Glove Award 2008.
 
Deadline for Abstracts: 2010-10-11
 
Registration:

  Live live online training only for one participant
Price: $195.00

Corporate Live 4 to 10 participants from a single location (For multiple locations contact Customer Care)

Price: $895.00

 

E-mail: webinars@GlobalCompliancePanel.com
 
   
 
home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
 
 
 

Generated by meetings and positions 5.0 by Kai Garlipp
WWW: Kai Garlipp, Frank S. Zollmann.
7.0 © 1995- HUM-MOLGEN. All rights reserved. Liability, Copyright and Imprint.