Tuesday, February 25, 2014

Budgeting for Clinical Trials: Understanding Costs of a Study and Which Costs Sponsors are Responsible to Cover

February 25, 2014 from 10am to 11am – Online Event This 90-minute webinar will help you understand what the true costs are for completing a clinical study and the unanticipated costs that may arise. You will learn about costs that a sponsor must incl… Organized by ComplianceOnline | Type: clinical
Automating Laboratory Assays For the Bench

February 25, 2014 from 10am to 11am – Online Event This webinar on automating laboratory assays will teach you how to translate an assay that is performed manually to one that is fully automated, with high quality and with proper validation and quali… Organized by ComplianceOnline | Type: medical
Pharmaceutical Government Price Reporting: Impact of Obamacare

February 25, 2014 from 10am to 11am – Online Event This webinar on drug price reporting will discuss the changes to the Medicaid Drug Program and its impact on pharmaceutical and biotech companies. Why Should You Attend: The Medicaid Drug Program is… Organized by ComplianceOnline | Type: pharmaceutical
Archiving Clinical Trial Documents - Understanding Regulatory Requirements for Paper and Electronic Records

February 25, 2014 from 10am to 10am – Online Event This webinar will cover regulatory requirements for archiving clinical trial documents, both paper and electronic records. It will focus on the key components of a digital preservation strategy to en… Organized by ComplianceOnline | Type: clinical
Cal/OSHA Inspections and Citations - Proven Strategies for Success

February 25, 2014 from 10am to 11am – Online Event This webinar will review recent inspection focus areas by Cal-OSHA inspectors, discuss how you should prepare for the inspection, and demonstrate proven strategies that will help you be successful bo… Organized by ComplianceOnline | Type: healthcare
Webinar On - Submitting FDA Electronic Regulatory Filings – Drug Establishment Registrations and Drug Listings

February 25, 2014 from 12pm to 1pm – Online Description : FDA gives a number of reasons for the decision to move away from paper submissions. These include: electronic review of drug labels for compliance, elimination of data entry errors, and… Organized by compliancetrainings | Type: online, training