How can you be you are compliant with all regulations when there are so many to manage? Learn how leading life sciences companies are using new processes, as well as new technologies to create tailor-made solutions, enabling global strategies in regulatory operations in this complimentary on-demand webinar: http://ap.pn/2eLrMAP

1. WHY IS REGULATORY INFORMATION
MANAGEMENT IMPORTANT?

2. At Appian, we regularly work with multinational
pharmaceutical companies, serving over
150 different countries.
With so many different regulations,
how do you comply with them all?

3. For example:
Data silos across many countries
creates a lack of visibility.
This blind approach can lead to
companies being put in global risk.

4. To eliminate manual,
mistake-prone
tracking sheets
To reduce risk
for companies across
hundreds of
global regulations
To bring new drugs
to the market faster
What are our goals?

5. We achieve this
by unifying all available data.
Put simply, we find that greater control over information
leads to a more efficient business.

6. Our compliance has helped thousands of products
in over 150 countries.
We have been able to balance compliance, regulations, and product
quality, all while getting products to market as quickly as possible.

7. Our methods have meant
that our clients
Submission quality
Regulation compliance
to over 99%
have increased: while decreasing:
Time for products
to reach markets
Organizational complexity
System maintenance costs

8. With Appian, we have simplified
our end to end business processes, and created
a single authoritative source of truth.
We needed a new regulatory submission management
platform that combined quality and compliance with the flexibility
to bring each new drug to market as quickly as possible.

9. only an integrate system can help it grow.
We achieve this
by unifying all available data.
Put simply, we find that greater control over information
leads to a more efficient business.

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