Clinical Regulatory Medical Writing Forum

Time:July 10-11, 2014

Country&Region: United States

Venue:Philadelphia, PA

Clinical Regulatory Medical Writing Forum

In today’s marketplace, there are an increasing amount of products going through the complex process of clinical trials and regulatory procedures that lead to market approval. The constantly tightening and changing guidelines being implemented by regulatory agencies make the approval process significantly more complex. These factors are resulting in a demand for articulate medical writers whom are knowledgeable and have the ability to successfully navigate these complex process and changing regulatory guidelines.

The Clinical Regulatory Medical Writing Forum is to educate Medical Writers on how to compose clear and comprehensive regulatory documents pursuant to the strict and continuously changing guidelines of regulatory agencies.

Top Five Reasons to Attend:

Learn best practices to effectively compose global regulatory submissions

Interpret the changing guidelines regarding data disclosure and transparency

Gain strategies to to efficiently handle protocol deviation

Effectively utilize graphics in Clinical Regulatory Medical Writing

Maintain effective partnerships when outsourcing medical writing

Contact:sponsor

Tel:866-207-6528

Website:http://www.exlpharma.com/medwrite

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