Whether your medical writers are in-house or external, or important documents have been acquired through a partnership, merger, or acquisition, managing electronic documents effectively is an essential part of getting your drug to market on time and keeping it there.
During this webinar, expert Mauricha Marcussen, Owner and Principal Consultant of Agano Solutions, LLC, will teach attendees how to effectively manage electronic documents. She will focus on establishing a quality control workflow between the medical writing community and regulatory affairs, and developing a plan for effectively leveraging improvements in the quality process upstream, through reporting, feedback and analysis.
In 90 minutes you will:
- Explore the needs of regulatory affairs professionals and the medical writing community in regards to the delivery of comprehensive, quality content
- Uncover document-related risks associated with the submission process
- Identify challenges in the formatting process
- Define business drivers that support an optimal environment while alleviating risk
- Highlight the importance of establishing a quality control workflow
- Learn how to position a plan for effectively leveraging improvements in the quality process
For one low price, you and your entire team can take part in this fast-paced, insightful webinar. Best of all, you’ll be able to connect personally with our speaker, Mauricha Marcussen, when we open up the phone lines for live Q&A.
July 12, 2012
1:00 PM ET / 10:00 AM PT
90 minutes
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