Regulatory Submissions, Information, and Document Management Forum

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On Demand 7: International Regulatory Update

Session Chair(s)

Michiel Stam

Management Consultant

MAIN5 Gmbh & Co. Kgaa, Germany

Receive the latest updates from International Regulators about recent and future developments related to data standards, analytics, electronic submissions, and Health Authority IT programs.

Learning Objective : At the conclusion of this session, participants should be able to:
Define future developments in the area of regulatory submissions, data standards and analytics at the regulator side

Describe and identify with the future objectives of the regulators

Speaker(s)

Speaker

Shannon Laforce, MBA

Health Canada, Canada

Executive Director, Transformation and Business Informatics, RMOD, HPFB

Speaker

Representative Invited

Medicines and Healthcare Products Regulatory Agency (MHRA), United Kingdom

Speaker

Jesper Kjær, MS

Novo Nordisk, Denmark

Global Director for Public, Private Partnerships, Strat Ops, Global Med Affairs

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Regulatory Submissions, Information, and Document Management Forum

On Demand 7: International Regulatory Update

Session Chair(s)

Michiel Stam

Learning Objective : At the conclusion of this session, participants should be able to: Define future developments in the area of regulatory submissions, data standards and analytics at the regulator side Describe and identify with the future objectives of the regulators

Speaker(s)

Speaker

Speaker

Speaker

Be informed and stay engaged.

Learning Objective : At the conclusion of this session, participants should be able to:
Define future developments in the area of regulatory submissions, data standards and analytics at the regulator side

Describe and identify with the future objectives of the regulators