Optimizing Medical Device Development with Full Regulatory Compliance

When developing highly complex and regulated product with an increasingly global workforce and widespread network of contractors and suppliers, quality is often sacrificed in the name of profitability, or time to market – sometimes with disastrous results. There is a need to eliminate organizational boundaries in order to accelerate the release of new products to market. Unfortunately, companies often address product quality too late, using disjointed processes and technologies with inadequate cross-functional communication.

Integrating a quality lifecycle management solution within an enterprise business platform provides a formalized, systematic approach for managing all aspects of product quality, reliability, and risk. It’s time to rethink your product development approach and look for a business platform that supports the full total product lifecycle from ideation through manufacturing and post-market and shares quality information across the enterprise.

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7 Risks of Regulatory Reporting

When it comes to financial disclosure, the devil’s in the details. An extra zero here, a negative number made positive there, an overlooked revision or two – stake holders are unimpressed with these simple human errors. To err is human, so let’s see where automation can replace manual processes.

When you automate once manual processes in the Disclosure Management Cycle, it not only prevents human errors, but also ensures seamless internal and external reporting practices. Read this whitepaper to identify seven common scenarios that result in error and the ideal solution for each.

What You’ll Learn:

  • How a single version of the truth can solve most of your reporting woes.
  • The best way to incorporate approvals into your workflow.
  • Why a single data source is the best way to update all reports and presentations.
  • The essential tools you need to create quality disclosures.

Download 7 Risks of Regulatory Reporting and share with your team today.

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Management Reporting: Let’s Stop Reinventing the Wheel

Yet, for many departments, report building is often a tedious, time-consuming, and error-prone process consisting of complex, manual tasks which lead to inaccurate, out-of-date and inconsistent reports across different lines of business. This white paper explores how you can reduce your internal reporting risk and build a repeatable, scalable process.

What You’ll Learn:

  • How to apply a factory approach to assembling text, narrative, and analysis
  • The steps to developing an automated assembly line for report production
  • Specific report workflows you should automate to mitigate risk

Download Management Reporting Let’s Stop Reinventing the Wheel.

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Optimizing Medical Device Development with Full Regulatory Compliance

When developing highly complex and regulated product with an increasingly global workforce and widespread network of contractors and suppliers, quality is often sacrificed in the name of profitability, or time to market – sometimes with disastrous results. There is a need to eliminate organizational boundaries in order to accelerate the release of new products to market. Unfortunately, companies often address product quality too late, using disjointed processes and technologies with inadequate cross-functional communication.

Integrating a quality lifecycle management solution within an enterprise business platform provides a formalized, systematic approach for managing all aspects of product quality, reliability, and risk. It’s time to rethink your product development approach and look for a business platform that supports the full total product lifecycle from ideation through manufacturing and post-market and shares quality information across the enterprise.

Request Free!