Pharmaceutical Regulatory Affairs Course in the Middle East, Dubai (Dubai, UAE - October 18-19, 2015)
DUBLIN, Sep. 02, 2015 /PRNewswire/ --
Research and Markets (http://www.researchandmarkets.com/research/b2ndv7/pharmaceutical) has announced the addition of the "Pharmaceutical Regulatory Affairs in the Middle East, Dubai (Dubai, UAE - October 18-19, 2015)" conference to their offering.
An Essential Course for Ensuring Compliance with Regulatory Requirements
Particularly relevant for Pharmacovigilance, Regulatory Affairs, Clinical Research/Operations, GMP, QA and Document Management Functions & Regulatory Authorities
Topics to be covered include:
- How to Write Concise and User Friendly SOPs
- Understand How to Prepare the Content of SOPs
- Implement, Manage and Review SOPs Effectively
- Ensure your SOPs Incorporate Appropriate Regulatory Requirements
- Design Effective SOP Training
Why You Should Attend
SOPs play a crucial role in compliance with regulations. It is therefore essential that they are well written and easy to use by the end-users. If SOPs are not followed correctly, the validity of data generated is compromised, leading to inspection findings and non-compliance issues which could lead to delays in bringing a drug/device to market.
This SOP course has been specifically designed to help you develop the skills to write and produce the content of SOPs, review and implement SOPs to ensure you are able to comply in a regulated environment. You will come away with the confidence to use a process to write, update and implement SOPs which can easily be used by the end users.
For more information visit http://www.researchandmarkets.com/research/b2ndv7/pharmaceutical
Media Contact: Laura Wood , +353-1-481-1716, [email protected]
SOURCE Research and Markets
Related Links
http://www.researchandmarkets.com
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