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#20: The Sunshine Act: Understanding the Essentials of Compliance

Dates

26 jun 2016 – 26 jun 2016

Location

Track 10 - Public Policy/Health Care Compliance/Law

Precio de lista:

$405
#21: Leadership: How to Organize and Lead People in a Work Group

Dates

26 jun 2016 – 26 jun 2016

Location

Track 16 - Professional Development

Precio de lista:

$405
#22: Successful Drug Development: Best Practices for Clinical Trial Design, Agency Interactions, and Regulatory Document Writing

Dates

26 jun 2016 – 26 jun 2016

Location

Track 08 - Regulatory Affairs

Precio de lista:

$405
#23: How to Prepare for an FDA Inspection

Dates

26 jun 2016 – 26 jun 2016

Location

Track 11 - Innovative Approaches to Ensuring Quality in Clinical Trials and Compliance to Good Clinical Practice (GCP)

Precio de lista:

$405
#23: How to Prepare for an FDA Inspection

Dates

26 jun 2016 – 26 jun 2016

Location

Track 11 - Innovative Approaches to Ensuring Quality in Clinical Trials and Compliance to Good Clinical Practice (GCP)

Precio de lista:

$405
#24: Regulatory Considerations for Drug and Medical Device Development: Current Status and Trend of IND/NDA Practices in China

Dates

26 jun 2016 – 26 jun 2016

Location

Track 08 - Regulatory Affairs

Precio de lista:

$405
#25: Signal Detection: Identifying and Managing Safety Signals

Dates

26 jun 2016 – 26 jun 2016

Location

Track 14 - Clinical Safety and Pharmacovigilance

Precio de lista:

$405
#30: Japan Regulatory Environment: Overview of the Organization, Processes, Systems, and Changes Affecting Pharmaceutical Development

Dates

26 jun 2016 – 26 jun 2016

Location

Track 08 - Regulatory Affairs

Precio de lista:

$405
#31: Preparing for a US FDA Advisory Committee Meeting

Dates

26 jun 2016 – 26 jun 2016

Location

Track 08 - Regulatory Affairs

Precio de lista:

$405
#32: Influencing Culture, Avoiding Bureaucracy, and Encouraging Innovation

Dates

26 jun 2016 – 26 jun 2016

Location

Track 16 - Professional Development

Precio de lista:

$405
#33: Preparation of Risk Evaluation and Mitigation Strategies Assessment Reports

Dates

26 jun 2016 – 26 jun 2016

Location

Track 14 - Clinical Safety and Pharmacovigilance

Precio de lista:

$405
#34: Ethical Issues in Clinical Trials

Dates

26 jun 2016 – 26 jun 2016

Location

Track 08 - Regulatory Affairs

Precio de lista:

$405
#37: Implementing a Risk-Based Monitoring Solution: Understanding the Basics of a Sustainable Model

Dates

26 jun 2016 – 26 jun 2016

Location

Track 01 - Clinical Operations

Precio de lista:

$405
#40: Analysis of Safety Data from Clinical Trials

Dates

26 jun 2016 – 26 jun 2016

Location

Track 15 - Statistical Science and Quantitative Thinking

Precio de lista:

$755
#41: A Rare Disease Program Case Study: Strategies for Successful Outcomes

Dates

26 jun 2016 – 26 jun 2016

Location

Track 17 - Rare/Orphan Diseases

Precio de lista:

$755
#42: Clinical Statistics for Nonstatisticians

Dates

26 jun 2016 – 26 jun 2016

Location

Track 15 - Statistical Science and Quantitative Thinking

Precio de lista:

$755
#43: Risk Management and Safety Communication Strategies

Dates

26 jun 2016 – 26 jun 2016

Location

Track 14 - Clinical Safety and Pharmacovigilance

Precio de lista:

$755
#44: The Good Pharmacovigilance Practices in the EU: Global Applications

Dates

26 jun 2016 – 26 jun 2016

Location

Track 14 - Clinical Safety and Pharmacovigilance

Precio de lista:

$755

Preconference Tutorials

Increase your knowledge in a small group setting. Register for a half day or full day preconference tutorial.

Tutorials require a separate registration and fee.

Preconference Tutorials

Increase your knowledge in a small group setting. Register for a half day or full day preconference tutorial.

Be informed and stay engaged.