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$189

Issue & Crisis Management; Capabilities that all FDA-regulated Businesses Should Have

Live Tuesday, May 28, 2013
01:00 | 02:00 PM - EDT , 60 Minutes
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$189

Strategic Portfolio Planning for Global Drug Development – approaches, techniques, tools

Live Wednesday, May 29, 2013
12:30 | 01:30 PM - EDT , -660 Minutes
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$189

Corrective Actions – what’s new from ISO 13485 auditors and FDA

Live Wednesday, May 29, 2013
02:30 | 03:30 PM - EDT , 60 Minutes
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$189

Key Issues in FDA & FTC Regulation of Dietary Supplements

Live Thursday, May 30, 2013
01:00 | 02:00 PM - EDT , 60 Minutes
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04

Serious Product Quality Problems – Dealing with the Press and the Public

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05

Clinical trial regulations, GCP compliance and FDA inspections

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06

Shared facilities and the move to science based risk assessments

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11

New HIPAA Breach Notification Standards - Tougher Rules Require Risk Assessment

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12

Good Laboratory Sanitation and Chemical Safety

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18

Premarket Submission, Validation & Cubersecurity for Software in Medical Devices

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19

Hosting Regulaotory Audits (fda, emea & health canada)

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20

Optimal capacity planning and resource allocation for a portfolio of clinical trials

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