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Tuesday, 14 November 2017

7:00

Registration and Welcome Refreshments

8:00

Chairperson’s Welcome and Opening Remarks

Kristin Buske
Principal Consultant
qordata

CREATING THE ROADMAP TO GDPR

8:15

Key Regulatory Concepts for Life Sciences Organisations

Mukundan Bharathan
Regional General Counsel – Europe
Dr. Reddy’s Laboratories SA

9:00

Unearthing Failures and Successes — Sharing an Example of
GDPR Implementation in Multiple Countries (Nordics)

Nicolai Ellehuus
Head, Legal and Compliance
Mundipharma Nordics

10:00

Networking and Refreshment Break

10:30

Excavate the Fundamentals for a Successful Consent Management Programme

Kristin Buske
Principal Consultant
qordata

Elisabeth Kohoutek
Associate, FDA and Life Sciences
King & Spalding

11:15

Strategies for Vendor Selection and Compliance

Elisabeth Kohoutek
Associate, FDA and Life Sciences
King & Spalding

12:00

Networking Luncheon

13:15

Privacy Trainings, Certification and Creating a Data Protection Officer (DPO) Toolbox

Maite Vázquez
Partner
Dutilh Abogados

Chain Reaction Power Panel

14:00

Examine the Key Risks for Your GDPR Programme

Based on the morning’s presentations and livepolling, an expert panel provides a review and discussion of the most pressing and controversial topics of the day. During this session, attendees have the opportunity to pose questions to the panel and each other for further benchmarking in support of GDPR compliance.

MODERATOR:

Mohammad Ovais
CEO
qordata

PANELISTS:

Anna Dolinsky
Associate General Counsel
Novo Nordisk A/S

Mukundan Bharathan
Regional General Counsel – Europe
Dr. Reddy’s Laboratories SA

Michael O’Connor
former Global Head Compliance and Ethics Operations
Alexion

14:45

Networking and Refreshment Break

15:15

Assessing the Impact of GDPR on Clinical Trials

Nick Tyler
Senior Director & Global Lead, Data Privacy
Takeda Pharmaceuticals

16:00

The Potential Impact of the GDPR on Data Transfers Between the
EU and Third Countries

Francis P. Crawley
Executive Director
Good Clinical Practice Alliance – Europe (GCPA), Brussels Belgium

Case Study

16:45

Learn Best Practices for Approaching a Data Breach

During this case study, walk through a hypothetical data breach based on the experience from one pharmaceutical company and learn strategies for proper compliance with requirements.

Anna Dolinsky
Associate General Counsel
Novo Nordisk A/S

17:30

Close of Bootcamp

Networking, Wine and Cheese Reception immediately following the final session

Want more agenda details? Download the brochure.

Tuesday, 14 November 2017

7:00

Registration and Welcome Refreshments

8:00

Chairperson’s Welcome and Opening Remarks

Kristin Buske
Principal Consultant
qordata

CREATING THE ROADMAP TO GDPR

8:15

Key Regulatory Concepts for Life Sciences Organisations

Mukundan Bharathan
Regional General Counsel – Europe
Dr. Reddy’s Laboratories SA

9:00

Unearthing Failures and Successes — Sharing an Example of
GDPR Implementation in Multiple Countries (Nordics)

Nicolai Ellehuus
Head, Legal and Compliance
Mundipharma Nordics

10:00

Networking and Refreshment Break

10:30

Excavate the Fundamentals for a Successful Consent Management Programme

Kristin Buske
Principal Consultant
qordata

Elisabeth Kohoutek
Associate, FDA and Life Sciences
King & Spalding

11:15

Strategies for Vendor Selection and Compliance

Elisabeth Kohoutek
Associate, FDA and Life Sciences
King & Spalding

12:00

Networking Luncheon

13:15

Privacy Trainings, Certification and Creating a Data Protection Officer (DPO) Toolbox

Maite Vázquez
Partner
Dutilh Abogados

Chain Reaction Power Panel

14:00

Examine the Key Risks for Your GDPR Programme

Based on the morning’s presentations and livepolling, an expert panel provides a review and discussion of the most pressing and controversial topics of the day. During this session, attendees have the opportunity to pose questions to the panel and each other for further benchmarking in support of GDPR compliance.

MODERATOR:

Mohammad Ovais
CEO
qordata

PANELISTS:

Anna Dolinsky
Associate General Counsel
Novo Nordisk A/S

Mukundan Bharathan
Regional General Counsel – Europe
Dr. Reddy’s Laboratories SA

Michael O’Connor
former Global Head Compliance and Ethics Operations
Alexion

14:45

Networking and Refreshment Break

15:15

Assessing the Impact of GDPR on Clinical Trials

Nick Tyler
Senior Director & Global Lead, Data Privacy
Takeda Pharmaceuticals

16:00

The Potential Impact of the GDPR on Data Transfers Between the
EU and Third Countries

Francis P. Crawley
Executive Director
Good Clinical Practice Alliance – Europe (GCPA), Brussels Belgium

Case Study

16:45

Learn Best Practices for Approaching a Data Breach

During this case study, walk through a hypothetical data breach based on the experience from one pharmaceutical company and learn strategies for proper compliance with requirements.

Anna Dolinsky
Associate General Counsel
Novo Nordisk A/S

17:30

Close of Bootcamp

Networking, Wine and Cheese Reception immediately following the final session