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Whitepaper

Applying FDA Regulations to Online Marketing

November 9, 2009

This guide aims to provide pharma marketers with an overview of the key challenges surrounding Direct-to-Consumer (DTC) online marketing and some potential solutions for effectively leveraging this channel within the complex regulatory environment.

Professional Scientific StaffingSM Solutions

October 21, 2009

Lancaster Laboratories Professional Scientific StaffingSM service has been specifically designed to give you the non-permanent workforce you need for anywhere from one year to 10 years or more with no worries about co-employment and at lower costs than fixed headcounts.

Physician Spend Management: How Health and Life Sciences Companies Can Simplify Compliance with Master Data Management

September 8, 2009

Many state-level governments have adopted legislations that limit as well as mandate the disclosure of payments to physicians.

The Executive Guide to Contracts & Chargebacks Management

September 1, 2009

When it comes to Contracts and Chargebacks - the stakes are high - as credits for chargebacks can often exceed millions of dollars each month. If you find yourself faced with addressing changing regulatory requirements, managing hundreds of contracts, and validating and processing chargeback submissions, we encourage you to learn more in this white paper.

Interoperability and Architecture for the Life Sciences Industry

May 28, 2009

Information technology is finally up to the task of cost-effective clinical research. But there are still some significant barriers to gaining all the benefits of the technology, in particular, interoperability. This white paper explores the need for a consistent industry architecture that allows life sciences firms to connect their enterprises and benefit from unified data integration, process consistency and rapid communication of meaningful drug findings.

How can we streamline late-stage clinical development processes to speed regulatory submissions and approvals?

May 28, 2009

This solution brief explains how SAS solutions streamline and accelerate drug development through better data integration and analysis. The brief explains the features and benefits of the SAS framework and includes a case study documenting the success of a top ?ten pharmaceutical company using the solution.

Managed Innovation, Assured Compliance

May 28, 2009

This white paper shows how to develop, execute and manage the transformation, analysis and submission of clinical research data with SAS® Drug Development. It includes an executive summary that outlines current industry challenges. And, it answers the top ten questions life sciences executives confront when trying to balance innovation with regulatory compliance.

Business Analytics: Six Questions to Ask About Information and Competition

May 28, 2009

Concise Executive Guide to Business Analytics: Overview of business applications and payoffs, staff and technology requirements, and the roles executives must play to realize the performance potential of analytics. Six key questions are asked about how well information at hand is used to meet goals and innovate in the marketplace.

Protecting Sensitive Information in Life Sciences Organizations: Top Three Misconceptions that Put Companies at Risk

May 26, 2009

Because of their investment in intellectual property and the clinical trial information they generate, life sciences companies face greater security risks than other companies. This paper explores common business processes that put companies at risk and ways companies protect themselves.

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