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Subject: Vendor and Supplier Qualification Program for FDA Regulated
 Industries | Early Registration Open
From: compliance seminar  <training@info.complianceonline.com>
To: charley@transocean.com
Date: Fri, 20 Apr 2018 14:26:00 +0000
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 Content preview:  ComplianceOnline ComplianceOnline The Largest GRC Advisory
    Network +1-888-717-2436 Vendor and Supplier Qualification Program for FDA
    Regulated Industries 2-Day In-Person Seminar Boston, MA | June 28-29, 2018
    • View Agenda Speaker: Dan O'Leary, President at Ombu Enterprises, LLC
   This workshop explains an overarching supplier qualification program that
   is common to FDA regulated medical product manufacturers. It also provides
    the details of the various program areas such as devices, pharmaceuticals,
    etc. [...] 
 
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<td style=3D"font-family: Arial, Helvetica, sans-serif;" valign=3D"middle"=
><span style=3D"font-family: Impact; color: #1062b2; font-size: 24px;">Comp=
liance</span><span style=3D"font-family: Arial, Helvetica, sans-serif; font=
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l, Helvetica, sans-serif; font-size: 11px; color: #000;">The Largest GRC Ad=
visory Network </span></span></td>
<td colspan=3D"2" valign=3D"middle" align=3D"right"><span style=3D"font-fa=
mily: Arial, Helvetica, sans-serif; font-size: 18px;"><strong>+1-888-717-24=
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<td style=3D"font-family: Arial, Helvetica, sans-serif; color: #444444; ; =
font-size: 22=2E5pt;" valign=3D"top" align=3D"center"><strong>Vendor and Su=
pplier Qualification Program for FDA Regulated Industries </strong><br /> <=
span style=3D"font-size: 17=2E0pt; font-weight: bold;"><em>2-Day In-Person =
Seminar </em></span></td>
</tr>
<tr>
<td style=3D"font-family: Arial, Helvetica, sans-serif; color: #444444; fo=
nt-size: 11=2E5pt;" valign=3D"top" align=3D"center"><strong>Boston, MA | Ju=
ne 28-29, 2018 </strong> =E2=80=A2 <a href=3D"http://info=2Ecomplianceonlin=
e=2Ecom/T/v400000162e37295d78ba9376e966f4758/95bd4970324243390000021ef3a0bc=
c2/95bd4970-3242-4339-9661-110e2d97ac5a" target=3D"_blank" rel=3D"noopener =
noreferrer"><strong>View Agenda</strong></a></td>
</tr>
<tr>
<td style=3D"font-family: Arial, Helvetica, sans-serif; color: #444444; fo=
nt-size: 11=2E5pt; line-height: 18=2E0pt;" height=3D"40" align=3D"center"><=
strong>Speaker:</strong> <strong>Dan O'Leary</strong>, President at Ombu En=
terprises, LLC</td>
</tr>
<tr>
<td style=3D"font-family: Arial, Helvetica, sans-serif; color: #444444; fo=
nt-size: 11=2E5pt; line-height: 18=2E0pt;" valign=3D"top" height=3D"" align=
=3D"left">This workshop explains an overarching supplier qualification prog=
ram that is common to FDA regulated medical product manufacturers=2E It als=
o provides the details of the various program areas such as devices, pharma=
ceuticals, etc=2E <br /> <br /> An effective supplier qualification uses to=
ols and techniques=2E The workshop explains particularly relevant tools suc=
h as supplier audits, metrics, scorecards, acceptance verification, and cor=
rective action=2E These techniques help make the program FDA compliant and =
robust=2E <br />
<table width=3D"100%" cellspacing=3D"0" cellpadding=3D"0" border=3D"0">
<tbody>
<tr>
<td align=3D"right"><a href=3D"http://info=2Ecomplianceonline=2Ecom/T/v400=
000162e37295d78ba9376e966f4758/95bd4970324243390000021ef3a0bcc3/95bd4970-32=
42-4339-9661-110e2d97ac5a" target=3D"_blank" style=3D"font-family: Arial, H=
elvetica, sans-serif; font-size: 11=2E5pt;" rel=3D"noopener noreferrer"><st=
rong>Register Now</strong></a></td>
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<br /> <strong>Learning Objectives:</strong><br /> <br /> Participants lea=
rn the elements of an effective supplier qualification program for FDA regu=
lated medical products=2E
<ul style=3D"font-family: Arial, Helvetica, sans-serif; color: #444444; fo=
nt-size: 11=2E5pt;">
<li>Define a sustainable supplier qualification program</li>
<li>Understand how to set expectations and requirements</li>
<li>Learn how to identify potential suppliers</li>
<li>Understand methods to evaluate potential supplier=E2=80=99s for their =
ability to meet your requirements</li>
<li>Know how to select suppliers based on the evaluation</li>
<li>Learn the requirements to keep records - a key component for FDA compl=
iance</li>
<li>Learn sound methods to specify the products and services from supplier=
s</li>
<li>Understand how to evaluate received products and services, including s=
tatistical techniques</li>
<li>Learn the techniques to monitor and measure supplier performance</li>
<li>Understand how to re-evaluate suppliers and keep records</li>
<li>Learn methods to improve or replace poor performers</li>
<li>Understand supplier qualification tools including audits and performan=
ce evaluation</li>
</ul>
<strong>Speaker Profile: </strong><br /> <br /> <strong>Daniel O'Leary</st=
rong> has more than 30 years' experience in quality, operations, and progra=
m management in regulated industries including aviation, defense, medical d=
evices, and clinical labs=2E He has a Master's Degree in Mathematics, focus=
ing on logic and number theory=2E His professional experience relates to qu=
ality, regulatory, reliability, and operations management=2E Mr=2E O'Leary =
is a regular speaker at international conferences including ASQ, ISM, and R=
AMS=2E
<table width=3D"100%" cellspacing=3D"0" cellpadding=3D"0" border=3D"0">
<tbody>
<tr>
<td height=3D"15" align=3D"right"><a href=3D"http://info=2Ecomplianceonlin=
e=2Ecom/T/v400000162e37295d78ba9376e966f4758/95bd4970324243390000021ef3a0bc=
c4/95bd4970-3242-4339-9661-110e2d97ac5a" style=3D"font-size: 14px;" target=
=3D"_blank" rel=3D"noopener noreferrer"><strong>View Details</strong></a></=
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<td style=3D"border: #ACACAC dashed 1px; border-left: none; border-right: =
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arget=3D"_blank" rel=3D"noopener noreferrer">4th Annual Medical Device Summ=
it 2018 | San Francisco, CA | June 7-8, 2018</a></strong></td>
</tr>
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Palo Alto, CA 94303, USA | +1-888-717-2436<br /> <span style=3D"font-size: =
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