ComplianceOnline

Orchestrating the Integration of Multiple Technical Suppliers in a Clinical Trial

Instructor: Richard Barrett
Product ID: 700277
Training Level: Basic to Intermediate
  • Duration: 60 Min

recorded version

$249.00
1x Person - Unlimited viewing for 6 Months
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Recorded Link and Ref. material will be available in My CO Section

Training CD

$500.00
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(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

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Read Frequently Asked Questions

In this presentation we use the orchestra as an example of how multiple technical suppliers can work successfully together, how outcomes can be measured, and its direct application to clinical trials

Description

Time was when a clinical trial was resourced almost entirely from inside a pharmaceutical company clinical research department. Today many, if not all, functions are outsourced leaving the company to complete a clinical trial by managing multiple external suppliers.

Why Should You Attend:

All companies at some time experience difficulty in managing this arrangements and most express dissatisfaction with the experience if not the outcome. Does it have to be this way? Is there any where we can find help? In this presentation we use the orchestra as an example of how multiple technical suppliers can work successfully together, how outcomes can be measured, and its direct application to clinical trials.

Areas Covered in the Seminar:

  • Why the orchestra is a good metaphor for clinical trials
  • The importance of measuring outcomes
  • Harmony requires leadership
  • Harmony also requires teamwork
  • Communication through a common notation
  • Individual skill is essential
  • Practice makes perfect
  • Conclusion

Who will benefit?

  • Project team leaders
  • Project team members
  • Project planners
  • Procurement / outsourcing personnel
  • Quality managers
  • Financial controllers

Instructor Profile:

Richard’s background is mainly in the pharmaceutical sector where he held senior roles in Pfizer Global Research and Development and with Pfizer Corporate Marketing Ltd. He also worked in GlaxoSmithKline (GSK) where he managed toxicology research projects, and within the international sector of Covance, an American corporate contract research organisation.

His particular expertise is in establishing clinical laboratory processes that are central to regulatory approval and post marketing surveillance of pharmaceutical products.

Follow us :
ComplianceOnline Medical Device Summit 2017

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

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