GCP - Principles and Rationale

Understand GCP principles & considerations and gain an understanding of the rationale for the wide range of documentation associated with clinical trials.

9 Apr 2014 at Holiday Inn London - Bloomsbury, London, GB

Medical & Health Care, Pharmaceuticals/Drug Discovery

GCP - Principles and Rationale 9 Apr 2014 Holiday Inn London - Bloomsbury, London, GB
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Clinical investigation with (newly discovered) drugs involving human subjects is a precarious action and could lead to ethical dilemmas. It is important to know which parties are involved in clinical trials and what their responsibilities are, whilst being aware of the (inter)national laws and regulations. Directives for good clinical practice are recorded in the ICH-Good Clinical Practice (GCP) guideline.

SMi's masterclass hosted by ADAMAS Consulting will discuss the history of GCP requirements and the principles behind them. This will include an explanation of the documentation requirements associated with clinical trials and what purpose these documents serve. This course will reinforce the importance of keeping up-to-date with developments and ensure that you continue to evaluate research practices and make improvements where necessary.

Key benefits to this masterclass are:
• Understand GCP principles and considerations
• Gain an understanding of the rationale for the wide range of documentation associated with clinical trials
• Receive timely insight into the view the European inspector sees when looking through trial documentation
• Learn from a leading industry expert in this field
• CPD certified event

Price
Standard: £599

When
From: April 09, 2014 08:30
To: April 09, 2014 12:30
Where

Holiday Inn London - Bloomsbury, Coram St, WC1N 1HT, London, GB

Category

Medical & Health Care, Pharmaceuticals/Drug Discovery

Contact email
dlee@smi-online.co.uk

External link

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