Regulatory Information Management Webinar:
Understand the principles of RIM and the expected benefits in 30 mins.

With the increasing complexity of global regulatory requirements, effective Regulatory Information Management (RIM) is at the heart of the stakeholder decision-making process.

But why is this so important?

Dec 10th at 11 AM – 11:30 AM PST | 2 PM – 2:30 PM EST

Effective management of regulatory activities is essential for obtaining marketing authorizations for pharmaceutical products and maintaining those approvals across multiple countries and regions. In many companies, Regulatory Information Management is not well defined and may consist of collections of spreadsheets, homegrown databases, emails and ad hoc reports – each full of redundant and/or inconsistent data.

However, as product registrations become increasingly complex and volumes increase, companies are realizing that the ability to answer business-critical questions about all regulatory activity in an efficient and timely manner is critical to effective operations that ensure enterprise-wide compliance with current and emerging requirements like IDMP.

Using real-world examples, this webinar will help you understand the principles of RIM and the expected benefits for all companies, regardless of size or product portfolio.

Once registered, you will receive a confirmation email containing information on how to access the webinar

Understand the principles of RIM and the expected benefits in 30 mins.
Date and Time
Tue, Dec 10, 2019 02:00 PM - 02:30 PM EST
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Ennov: An intuitive and unified content and information management platform to support and enrich the entire Life Sciences product life cycle

Headquartered in Paris, with offices in the US and UK, Ennov provides the most original, comprehensive, and cost-effective suite of software solutions for the life sciences industry. From leading pharmaceutical companies to emerging biotechnology companies, we proudly serve over 150 companies and 150,000 users around the world.

For more than 20 years, we have been developing innovative, powerful and easy-to-use software for regulated content, data and process management. Our solutions are designed and built to support the entire Life Sciences R&D continuum including Clinical, Regulatory, Quality, Pharmacovigilance and Commercial.

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