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Non-Invasive Ventilation Print E-mail
Why the interest in Noninvasive ventilation?
  • Complications related to process of intubation and mechanical ventilation
  • Those caused by loss of airway defence mechanism
  • Those that occur after removal of the endotracheal tube
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Basic Mechanical Ventilation Print E-mail

Objective of Mechanical Ventilation:



  • The main indication for mechanical ventilation is respiratory failure, to improve gas exchange, to reduce the work of breathing and to avoid complications while maintaining optimal conditions for recovery.
  • Mechanical ventilation is an essential life-saving technology, however that influence the morbidity and mortality of patients receiving intensive care. Therefore, it was essential to use the safest and most effective form of ventilation for the shortest possible duration because of the potential complications and costs of mechanical ventilation.


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Good Clenical Practice (2 days) Print E-mail

Workshop – 1: Good Clinical Practice (GCP)

Day 1 (Thursday, 3 December 2009)

08.00 – 08.30 Registration

08.30 – 08.45 Welcome address by Dr. Yap Kok Wei,

  CEO, GleneaglesCRC Group,

  Group VP Research, ParkwayHealth, Singapore

08.45- 09.15 Overview of Drug Development & Clinical Research

Dr. Yap Kok Wei. CEO, GleneaglesCRC Group,

Group VP Research, ParkwayHealth, Singapore

09.15 – 09.45 Overview of ICH-GCP Guidelines

Ms. Azizah Mohamed, IRB Member

Parkway Independent Ethics Committee, Singapore

09.45 – 10.15 Exercise 1: ICH-GCP Guidelines

GCRC

10.15 – 10.45 Morning refreshments

10.45 – 11.15 Ethics in Clinical Research and Role of Ethics Committee

Ms. Azizah Mohamed, Senior manager

Hospital Administration of Mount Alvernia Hospital, Singapore

11.15 – 11.45 Informed Consent Process

Ms. Angeline Lim, Senior Clinical Research Manager

Gleneagles CRC Pte. Ltd

11.45 -.12.15 Role and Responsibilities of Investigator

Ms. Angeline Lim, Senior Clinical Research Manager

Gleneagles CRC Pte. Ltd

12.15 -.13.00 Networking luncheon

13.00 – 14.00 Exercise 2 : Informed Consent

GCRC

14.00 – 14.30 Good Documentation and Archiving

Ms. Fabiola C.R Hutabarat, Senior Clinical Research Associate

Gleneagles CRC Pte. Ltd

14.30 – 15.00 Handling and Accountability of Clinical Trial Material

Ms. Fabiola C.R Hutabarat, Senior Clinical Research Associate

                    Gleneagles CRC Pte. Ltd

15.00 – 16.00 Q & A

16.00 – 16.30 Tea and End of session

Day 2 (Friday, 4 December 2009)

08.15 – 08.30 Registration

08.30 – 09.15 Clinical Research in Indonesia

  Dr. Lina Ratulangie, Medical Doctor

                     Taisho Pharmaceutical Indonesia (formerly BMS-Indonesia)

09.15 – 10.00 Regulatory Requirements of Clinical Trials in Indonesia

10.00 – 10.30 Role and Responsibilities of The Sponsor

Dr. Lina Ratulangie, Medical Doctor

                    Taisho Pharmaceutical Indonesia (formerly BMS-Indonesia)

10.30 – 11.00 Morning refreshments

11.00 – 11.30 Role and Responsibilities of the Study Site Coordinator

Ms. Angeline Lim, Senior Clinical Research Manager

Gleneagles CRC Pte. Ltd

11.30 – 12.00 Role and Responsibilities of the Site Study Monitor

Mr Rodmar Pulido, Country Manager

Gleneagles Clinical Research International Pte Ltd, Philippines

12.00 – 13.30 Networking luncheon

13.30 – 14.00 Safety Monitoring and Reporting

Mr Rodmar Pulido, Country Manager

Gleneagles Clinical Research International Pte Ltd, Philippines

14.00 – 14.30 Quality Assurance in Clinical Trials: Fraud and Misconduct

Mr Rodmar Pulido, Country Manager

Gleneagles Clinical Research International Pte Ltd, Philippines

14.30 – 15.00 Exercise 4: Case Studies on Fraud and Misconduct in Clinical           Trials GCRC

15.00 – 15.30 Q & A

15.30 – 15.45 Closing Remarks by Dr. Yap Kok Wei,

CEO, GleneaglesCRC Group,

Group VP Research, ParkwayHealth, Singapore

15.45 – 16.30 Multiple choice question examination for certification

16.15 – 16.45 Participants Evaluation & Farewell Tea

End of session

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