Nov 18 2009

Events

@ 4:27 pm

Webinar Course Highlights for Month of May, 2010

10% discount if used before May 31, 2010 Promo Codes: 93490

Date Topic Speaker
20-May-10

How
to successfully audit software systems, and thereby avoid having FDA
write software-related 483′s and warning letters

 

 Dennis Moore
20-May-10

Improving
Sanitation Standard Operating Procedures In the Food Industry

 

 Angeline Benjamin
20-May-10

The
role of Analytical Program to Support Drug Development Process

 

 Kim Huynh-Ba
21-May-10

Method
Verification according to <1226> – Why and How – Verification
of Compendial Methods

 

 Nanda Subbarao
25-May-10

Webinar
on Risk-Based CAPA (Corrective and preventive action) Systems

 

 John E Lincoln
25-May-10

Managing
Out of Trend Results in Pharmaceutical Manufacturing and Quality Control

 

 Dr. Ludwig Huber
25-May-10

GCP/ICH
Obligations of Sponsors, Monitors, and Investigators- barriers and solution

 

 Sandy Rizk Soliman
25-May-10

Supplier
Evaluation and Assessment Program: How to meet FDA QSR and ISO 13485
requirements in a cost effective manner

 

 Jeff Kasoff
26-May-10

FDA
Warning Letter Closeout Program

 

 Alfonso Fuller
26-May-10

Potency
determination of drugs and biologics: design, and development of reliable
potency bioassays

 

 Chitra Edwin
26-May-10

You
have a sterility or Bioburden test failure – Now what?

 

 Gerry O Dell
26-May-10

Why
Pharmacovigilance (Phase IV Trials) will be increasingly seen: What
do they tell us and why are they important?

 

 Charles H Pierce
26-May-10

Reducing
Ethylene Oxide (EO) Sterilization costs while maintaining regulatory
compliance

 

 Marisel Ortiz
26-May-10

Fraud
& Abuse in healthcare sales and marketing – Update on the Law and
Tips on Compliance

 

 Mark DuVal,Mark Gardner
27-May-10

Conducting
Successful Product Complaint Investigations

 

 David Dills

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