- email:registration@pti-europe.co.uk
- phone:+44 (0) 20 7017 7481
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Regulatory Affairs for Clinical Trials
27 - 28 September 2012, MWB Victoria
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What Will You Learn?
Gain a comprehensive overview of the regulatory requirements for carrying out clinical trials
Gain a comprehensive overview of the regulatory requirements for carrying out clinical trials
Develop effective processes for obtaining clinical trials authorisation
Develop effective processes for obtaining clinical trials authorisation: Regulatory approval and ethical approval
Clarify the requirements for running clinical trials in children
Clarify the requirements for running clinical trials in children
Understand the most important legal aspects of clinical trials
Understand the most important legal aspects of clinical trials
Who Should Attend
The course is relevant for anyone involved with clinical trials or liaising/supporting Clinical research professionals in pharmaceutical, biotechnology CRO and SMO –companies, or study sites including investigator initiated studies.
The workshop will also be of interest to those departments who liaise with clinical trial personnel (such as regulatory affairs, clinical trial supply, quality assurance, document management, legal) and all other professionals who want to know more about regulations covering clinical trials.
Other Events That Will Interest You
Auditing Clinical Trials for GCP Compliance
19 Sep 2012 - 20 Sep 2012
Regus Princeton - Forrestal Village, New Jersey, USA
Reviews
"Good course!"
"Very good course and speaker"
"Lots of information provided- very good"
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Dates and Venues
23 Apr 2012 - 24 Apr 2012
MWB Victoria
27 Sep 2012 - 28 Sep 2012
MWB Victoria
Connect with the PTI faculty! PTI is a global pharmaceutical training company with over 60 interctive courses focusing on Regulatory Affairs, R&D, Clinical, Business Strategy, Fine Chemicals, Biopharmaceuticals, Manufacturing, Medical Devices and Agrochemicals
