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Subject: Final Call for Validation of HPLC/UPLC Methodologies
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Live Webinar | Speaker: John Fetzer

Validation of HPLC/UPLC Methodologies

Date:  Apr 20, 2023, | Time:  01: 00 PM EST | Duration: 90 Minutes

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Instrumental liquid chromatography is an analysis widely used to determine purity, impurities, and the degradation products of pharmaceuticals. The focus of most validation work is on the methodology, the standard operating procedure (SOP). But validation of the instrumentation and other associated items of the column,  solvents, and other reagents and chemicals is also an area of focus in an audit.

Areas Covered:-

- Instrument validation
	- The pumping system
	- The column
	- The detection system
	- The Data System
	Method validation
	- Precision and the various measures of precision (repeatability, reproducibility, ruggedness, robustness)
	- Limits of detection and quantitation, linearity
	- Selectivity, interferences, and specificity
	- Sensitivity
	- Solution stability
	- Accuracy
Background:-

Instrumental liquid chromatography, either as HPLC or UPLC, are a common technique in laboratories that do regulatory-compliance work. For Good Laboratory Practice (GLP) or for ISO 17025 compliance, such methods must meet certain requirements. This presentation will cover the key elements to have a compliant method.

Why Should You Attend:-

In order to meet US EPA or FDA requirements, a method must meet many stringent requirements. The more important of these for specific analytical methods are method validation and instrument validation. To not do so is a non-compliance in which any data is not usable or reportable.

For more for 6+ attendees call us at +1-844-899-4647 or mail us at cs@profeducations.com

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                                                  <table cellpadding="0" cellspacing="0" width="100%" role="presentation" style="min-width: 100%; " class="stylingblock-content-wrapper"><tr><td class="stylingblock-content-wrapper camarker-inner"><p style="text-align: center;"><span style="font-family: Georgia, serif; font-size: 16px;"><strong>Live Webinar |&nbsp;</strong><span style="color: rgb(184, 49, 47);"><strong>Speaker:</strong></span><strong>&nbsp;</strong></span><span style="font-size: 16px;"><strong>John Fetzer</strong></span></p>
<hr size="4" width="80%" color="red">
<p style="text-align: center;"><strong><span style="font-size: 20px;">Validation of HPLC/UPLC Methodologies</span></strong></p>
<p style="text-align: center;"><span style="font-size: 18px;"><span style="color: rgb(184, 49, 47);"><strong>Date:</strong></span><strong>&nbsp;&nbsp;</strong><strong>Apr 20, 2023, |&nbsp;</strong><span style="color: rgb(184, 49, 47);"><strong>Time:</strong></span><strong>&nbsp; 01: 00 PM EST |&nbsp;</strong><span style="color: rgb(184, 49, 47);"><strong>Duration:&nbsp;</strong></span><strong>90 Minutes</strong></span></p>
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<p style="text-align: center;"><a href="http://click.info.mailssenders.com/?qs=42dbfecd03e60d7a6a4f198decfdb3f24c731ba142a5cf18035599d4551e2b49ba8be16af9a3cf7d92083072379d2513cb2aa2dd6ef48b1f"><strong><span style="font-size: 22px;">Register Now</span></strong></a></p>
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                    <p style="text-align: center;"><strong><span style="font-size: 18px;">Get $29 off,</span></strong><span style="font-size: 18px;"> Use Code: <strong>&#39;PT2&#39;</strong> at checkout!</span></p>
                    <p><span style="color: rgb(0, 0, 0); font-size: 17px;">Instrumental liquid chromatography is an analysis widely used to determine purity, impurities, and the degradation products of pharmaceuticals. The focus of most validation work is on the methodology, the standard operating procedure (SOP). But validation of the instrumentation and other associated items of the column, &nbsp;solvents, and other reagents and chemicals is also an area of focus in an audit.</span></p>
                    <p><span style="color: rgb(0, 0, 0); font-size: 17px;"><strong>Areas Covered:-</strong></span></p>
                    <ul>
                        <li style="color: rgb(0, 0, 0); font-size: 17px;">Instrument validation<ul style="color: initial; font-size: initial;">
                                <li style="color: rgb(0, 0, 0); font-size: 17px;">The pumping system</li>
                                <li style="color: rgb(0, 0, 0); font-size: 17px;">The column</li>
                                <li style="color: rgb(0, 0, 0); font-size: 17px;">The detection system</li>
                                <li style="color: rgb(0, 0, 0); font-size: 17px;">The Data System</li>
                            </ul>
                        </li>
                        <li style="color: rgb(0, 0, 0); font-size: 17px;">Method validation<ul style="color: initial; font-size: initial;">
                                <li style="color: rgb(0, 0, 0); font-size: 17px;">Precision and the various measures of precision (repeatability, reproducibility, ruggedness, robustness)</li>
                                <li style="color: rgb(0, 0, 0); font-size: 17px;">Limits of detection and quantitation, linearity</li>
                                <li style="color: rgb(0, 0, 0); font-size: 17px;">Selectivity, interferences, and specificity</li>
                                <li style="color: rgb(0, 0, 0); font-size: 17px;">Sensitivity</li>
                                <li style="color: rgb(0, 0, 0); font-size: 17px;">Solution stability</li>
                                <li style="color: rgb(0, 0, 0); font-size: 17px;">Accuracy</li>
                            </ul>
                        </li>
                    </ul>
                    <p><span style="color: rgb(0, 0, 0); font-size: 17px;"><strong>Background:-</strong></span></p>
                    <p><span style="color: rgb(0, 0, 0); font-size: 17px;">Instrumental liquid chromatography, either as HPLC or UPLC, are a common technique in laboratories that do regulatory-compliance work. For Good Laboratory Practice (GLP) or for ISO 17025 compliance, such methods must meet certain requirements. This presentation will cover the key elements to have a compliant method.</span></p>
                    <p><span style="color: rgb(0, 0, 0); font-size: 17px;"><strong>Why Should You Attend:-</strong></span></p>
                    <p><span style="color: rgb(0, 0, 0); font-size: 17px;">In order to meet US EPA or FDA requirements, a method must meet many stringent requirements. The more important of these for specific analytical methods are method validation and instrument validation. To not do so is a non-compliance in which any data is not usable or reportable.</span></p>
                </section>
            </div>
        </div>
    </div>
</div>
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<p style="text-align: center;"><span style="color: rgb(0, 0, 0); font-size: 17px;"><strong>For more for 6+ attendees call us at +1-844-899-4647 or mail us at cs@profeducations.com</strong></span></p><img src="http://click.info.mailssenders.com/open.aspx?ffcb10-feca11747561037d-fe1a11767060007a721279-fe3311737164047c711374-ff2f17717d60-fe2313787166027d7c1272-ff911278&d=120012&bmt=0" width="1" height="1" alt=""></custom></td></tr></table><p style="text-align: center;">If you don't want to hear from us
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