Event:
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How To Translate Academic and Discovery Assays Into GLP
Compliant Assays
- Hosted By:
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ComplianceOnline
- Start:
- Wednesday - Mar 12, 2014 10:00 AM
- End Time:
- Wednesday - Mar 12, 2014 11:00 AM
- Location:
- Online
- This GLP compliant assay training will help attendees deal with the challenges and pitfalls that may occur when translating assays as demonstrated in the scientific literature or through internal discovery efforts.
Why Should You Attend:
Every day, there are a number of novel and interesting discoveries that are published in academic literature. Many of them, if proven to be true, will lead to improved industrial research and potentially improved human health. However, there is a dramatic difference in documentation standards between the academic world and the industrial world, and learning how to bridge that gap successfully will require strong investigational skills to find out what truly happened during the performance of the assay and the conditions therein needed to perform it.
This webinar will help attendees to fill in the gaps with confidence and learn what one needs to find out to shepherd key discoveries between worlds to ultimately further the goal of the biotechnology and pharmaceutical industries of improving human life.
Areas Covered in the Webinar:
This webinar will help attendees identify the key steps needed to be taken while transitioning a new assay from the academic world to the industrial world. The webinar will include the following critical information:
-What to look for in lab books and other notes to see what was performed
-How to ask academic scientific staff for other key information they may not realize is important
-How to determine whether a test is feasible for industrial usage, regardless of the technical validity of the test
-How to track down controls, reagents and test apparatus and test them using existing methods for suitability and quality
-How to develop the necessary reagents needed to perform the assay in an industrial context
-What kinds of repetition and repeatability studies are typically needed
Who will Benefit:
This topic applies to personnel / companies in the biotechnology and pharmaceutical industries. The employees who will benefit most include:
-Senior management
-Quality Assurance
-Research and Development
-Project management
- Website:
-
Visit the website for detail info