Date: 1st & 2nd November 2017
time: 8.30am
Venue: Lionel Memorial Auditorium, Sri Lanka Medical Association, No 6, Wijerama Mawatha, Colombo
Programme
Day 1: 1 st November 2017
Introduction
President SLMA
Introduction to GCP
Principles
What is GCP?
Need for GCP?
Prof Priyadarshani Galappaththy
Professor in Pharmacology
FM, Colombo
Drug development process
Dr Channa Ranasinha
Senior Lecturer in Pharmacology,
FM, Kelaniya
Investigational products
Prof Shalini Sri Ranganathan
Professor in Pharmacology
FM, Colombo
Clinical Trial protocol and IB
Dr Nirmala Wijekoone
Senior Lecturer in Pharmacology, FMS, USJ
Role and Responsibilities of PI
Dr Noel Somasundaram
Consultant Endocrinologist
Regulatory requirements for clinical trials and legal frame work
Mr Arjuna Pathmaperuma
Regulatory Pharmacist
NMDRA/ SCOCT
Role of the sponsor & CRO
Prof Vajira Dissanayake
Professor of Anatomy, FM, Colombo
Board member, FERCAP
Day 2 – 2 nd November 2017
Participant safety and adverse effects
Prof Shalini Sri Ranganathan
Professor in Pharmacology
FM, Colombo
Documentation & record keeping
Prof G R Constantine
Professor in Clinical Medicine, FM, Colombo
Research ethics in Clinical Trials
Prof Chandanie Wanigatunge
Chairperson, FERCSL
Chairperson, ERC SLMA
Ethics review committee – function with special ref to GCP and Clinical Trials
Dr Panduka Karunanayake
Senior Lecturer in Clinical Medicine, FM, Colombo
Secretary ERC, FM Colombo
Research misconduct and COI
Dr Malik Fernando
ERC, SLMA
Informed consent
Dr Manouri Gamage
Senior Lecturer, FMS, USJ