Applying New Technology in HPLC Methods for Improved Profit & Compliance

Duration: 60 Minutes
This webinar describes the application of new technology in HPLC methods to achieve over five-fold improvement in QC testing capacity, applying currently available materials and instruments. The new methods developed provide greater sensitivity, capacity, and may allow the ability to resolve new impurities, reducing risk from novel unknown impurities yet to be identified in raw material and products. The webinar describes the approach enabling users to attain these benefits readily, generally with existing instrumentation, although the availability of advanced UPLC instrumentation is demonstrated to provide even greater advantages.
New Technology in HPLC Methods
Instructor: Richard Youngstrom
Product ID: 501766
Objectives of the Presentation
  • Demonstrate the high and unacceptable cost of relaying on legacy methods for QC testing
  • Demonstrate advantages of new sorbent technology enabling new approaches to QC method development
  • Demonstrate new approaches to rapid sample preparation
  • Demonstrate the wide range of application of this approach across product lines
  • Demonstrate the benefits of using expanded capacity to enable new methods providing greater capacity and the ability to identify currently unknown impurities, helping the company avoid liability from recalls or adverse events
  • Demonstrate the advantages of incorporation of new instrumentation to achieve greater sensitivity and capacity in QC testing
Why Should you Attend
Participants will realize the impact of the new technology available and observe that these benefits are readily attainable with the application of the principles demonstrated in this presentation. All ARD and QC Directors, Managers, chemists and those involved in maximizing corporate laboratory productivity will benefit from observing the benefits of redeveloping methods using the procedures described to attain greater laboratory capacity and the ability to identify and reduce risks from unknown impurities which are not identifiable with existing legacy methods.

Areas Covered
  • Define legacy methods by function
  • Illustrate the inefficiencies inherent in reliance on legacy methods in the pharmaceutical industry
  • Illustrate the advantages of incorporating new technology into existing laboratory practices to achieve greater laboratory capacity and faster release testing
  • Illustrate the greater laboratory capacity available for multiple projects with the same resources
  • Illustrate the greater assurance of product quality available through greater resolution and sensitivity available from the application of the concepts described
  • Illustrate the greater compliance available through the improved control of materials tested with improved resolution and sensitivity provided by the methods developed using new technology
Who will Benefit
ARD and QC Directors, Managers, chemists and those involved in maximizing corporate laboratory productivity will benefit from observing the benefits of redeveloping methods using the procedures described to attain greater laboratory capacity and the ability to identify and reduce risks from unknown impurities which are not identifiable with existing legacy methods.

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  • Get answers to your queries through interactive Q&A sessions via chat at the end of the session
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account 24 hours after the completion of the session
  • Please let us know your thoughts and views at the end of the webinar, your valuable feedback will help us improve
Recorded Session - How it works
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  • Upon purchase of the recorded session a link will be updated on your OCP Account within 24 hours
  • Please click on the link to access the Recorded Session
  • Presentation handouts in downloadable PDF format will be updated on your OCP Account within 24 hours of the purchase of the product
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account after 48 hours of the product Purchase
  • Please share your valuable Feedback at the end of the session
Instructor Profile:
Richard Youngstrom is a Senior Compliance Consultant in the Pharmaceutical industry with extensive experience (30+ years) in GMP LaboratoryCompliance and Quality System improvements. In 2013, Richard retired from his position as Director of Quality Control at Braintree Laboratories and transitioned into Pharmaceutical consulting to help pharma clients meet current regulatory guidelines and improve laboratory compliance and efficiencies; i.e. leveraging his expertise in auditing, OOS laboratory & manufacturing investigations, training, and test method optimization to gain quality efficiencies.

Mr. Youngstrom started his career with Schering Corporation in early drug discovery, and advanced through several positions to Senior Group Leader in Radiochemistry. Richard's product line experience includes radiopharmaceuticals, APIs, solid and semi-solid dose formulations, liquids, transdermal products and OTC drugs.

He is also a certified technical trainer and has conducted FDA Analyst Certification programs for a number of companies. Utilizing his ASQ CQA and CPGP certifications, he has conducted a full range of audits including clinical audits, supplier qualification, general compliance audits, and for-cause corrective action audits, within the United States and internationally.


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