ComplianceOnline

Basic HPLC Theory and Method Development

Instructor: Jeff Phillips
Product ID: 700194
Training Level: Basic

recorded version

$249.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section

Training CD

$500.00
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-565-8542

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This HPLC theory (high performance liquid chromatography) training will cover the beginnings of HPLC through method validation and method development. Attention will be paid to understanding the thought process behind HPLC theory methods in the laboratory.

HPLC is a form of separation science that is arguably the most utilized form of analytical chemistry in the pharmaceutical industry. Yes, it is only a tool, but a powerful one that when used properly may be the workhorse QC technique or the sensitive and adaptable R&D system. This webinar will cover the begininnings of HPLC through method validation and method development. Attention will be paid to understanding the thought process behind HPLC methods in the laboratory. Also covered will be how it has been affected by and affected FDA and ICH guidelines.

Areas Covered in the Seminar:
  • How do you make a method and why are so many monographs combersome at best?
  • What is HPLC and how did it come about?
  • What are the pieces/ parts of an HPLC system?
  • How do you chose a column?
  • What information needs to be captured, recorded, kept and why?
  • The basics of method validation.
  • Why does pH and buffers matter?
  • What are some FDA rules and ICH guidelines?
Who Will Benefit:
This web seminar will train or refresh the partisipant in how HPLC works, why and what are the guidelines affecting the use of HPLC. Regulated companies in the pharmaceutical, biotechnological, and medical device industries will benefit from the webinar presentation. The people that will benefit the most include:
  • Scientists
  • QA managers and personnel
  • QC managers and personnel
  • Validation specialists
  • Consultants
  • Quality system auditors and vendor auditors

Instructor Profile
Jeff Phillips is a primary investor and Principal Consultant with Atzari Consulting. A firm that specializes in management consulting for the medical device, pharmaceutical, combination and biotechnology fields. Jeff started an analytical laboratory and established policy concerning the analysis of organic residuals. He has worked on HPLC systems since the late 1980’s and has over 10 years of experience in the pharmaceutical and medical device industries. He has tought many chemists and supervisors HPLC, and received an award from Wyeth for technical training. He has done technical training in the US and Europe.

Follow us :
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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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