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How Due Diligence in Accurate Adverse Event Reporting is the Key to a clean FDA Audit Subject: Why Should You Attend: Presently, there is an increase in real-time FDA...
Posted 10/6/2011 2:08:20 PM
Predicting Product Life Using Reliability Analysis Methods Subject: Why Should You Attend: When developing new products, it is imperative that...
Posted 10/6/2011 2:11:51 PM
FDA Warning Letter Closeout Program Subject: This FDA warning letter closeout program will discuss how to successfully...
Posted 10/6/2011 2:18:26 PM
3-hr Virtual Seminar: Outsourcing Medical Device Software Development with Compliance to IEC 62304 Subject: Why Should You Attend: In order for a medical device company to meet the...
Posted 10/6/2011 2:24:08 PM
Process Validation for Biological Products – Fitting PV into Process Development and QbD with New Regulations Subject: This Process Validation training for biological products will provide valuable...
Posted 10/6/2011 2:36:35 PM
FDA's 2011 Draft Guidance on Financial Disclosure by Clinical Investigators Subject: This webinar will help you understand FDA’s draft guidance on financial...
Posted 10/6/2011 2:40:14 PM
FDA's new enforcement initiative – Strategic Software Validation Planning for Executives and Managers Subject: This Software Validation training webinar will discuss how to approach Strategic...
Posted 10/7/2011 10:08:27 AM
Understanding and Implementing the Medical Device Directive Subject: Most medical devices marketed in the European Union must follow the Medical...
Posted 10/10/2011 11:43:55 AM
Full Day Virtual Seminar: Understanding and Effectively Controlling Biofilm in Pharmaceutical Water Systems Subject: This 6-hr training will focus on important microbial issues with pharmaceutical...
Posted 10/10/2011 12:01:07 PM
Application of CAPA to the Device Sterilization Process Subject: Do you use a Contract Sterilizer for your medical device sterilization? Are...
Posted 10/10/2011 12:11:24 PM

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