Return-Path: Delivered-To: charley@transocean.com Received: from vps.transocean.com by vps.transocean.com with LMTP id gP3KG2xa1lrmdAAAInt2oQ for ; Tue, 17 Apr 2018 13:34:52 -0700 Return-path: Envelope-to: charley@transocean.com Delivery-date: Tue, 17 Apr 2018 13:34:52 -0700 Received: from com8.compliance4all.com ([147.135.236.74]:51932) by vps.transocean.com with esmtps (TLSv1.2:ECDHE-RSA-AES256-GCM-SHA384:256) (Exim 4.89_1) (envelope-from ) id 1f8XJK-0007qb-NC for charley@transocean.com; Tue, 17 Apr 2018 13:34:52 -0700 DKIM-Signature: v=1; a=rsa-sha256; c=relaxed/relaxed; d=globalcompliancepanel.com; q=dns/txt; s=sarvtes; bh=W31sScR7epAY9xTv/iSnWmeYZU7PApL5ez2NZK2H8ik=; h=from:reply-to:subject:to:mime-version:content-type:list-unsubscribe; b=aamwKEhW7FzJ3gdYC+BTNobAETX4z2Ij1NdhMWVJBvxzz5ZgzAAZrY193d6RujqEXIf7HDJRP iFDgg8X3vskFrEScB86tbuUjxwZuG8kSQ9oDe5kbq6yAriukKtM6gUlIDkjYww6DqReuE5fsB9j /Jx/nHwgsEpFFUt4vBhhu5s= Content-Type: multipart/alternative; boundary="_----------=_MCPart_901487339" X-Unique-Id: 6f704109836ce7d232147ab8632d96fe80ea13cefb4b8975ae4a54c6fefba564c015b037f3c6af462661107be3ea5bac3d6f401db9d9290a151b7ef7c05299ed5a4162f09ddcbcf54fc1dbef04bc301e8737411bee7d50398800afaede0791c54a0ddf38b753046dfbfdecce07c47002c513b8172bae29f8306cb28f93e78c89 Precedence: bulk X-Feedback-Id: 10589302:5ad630181f2b1d184b8b45c0.5ad6314e43fd7ae45e1298f8:app:mg List-Unsubscribe: , Reply-To: inpersonseminar@globalcompliancepanel.com From: Statistics for FDA Process Validation To: charley@transocean.com Subject: Applied Statistics for FDA Process Validation Message-Id: <1523997165387-07dfaba0-196e8cd3-a9f7af41@globalcompliancepanel.com> Date: Tue, 17 Apr 2018 20:32:45 +0000 MIME-Version: 1.0 X-Mta-Unique-Id: tetttbse.sedqnttq--72410620-B7618664-2159-43BD-825A-1FE0EFC01DB8.5.1 Received: from (127.0.0.1) by com8.compliance4all.com id B7618664-2159-43BD-825A-1FE0EFC01DB8.5 for ; Tue, 17 Apr 2018 20:33:40 +0000 (envelope-from ) X-Spam-Status: No, score=1.2 X-Spam-Score: 12 X-Spam-Bar: + X-Ham-Report: Spam detection software, running on the system "vps.transocean.com", has NOT identified this incoming email as spam. The original message has been attached to this so you can view it or label similar future email. If you have any questions, see root\@localhost for details. Content preview: Applied Statistics for FDA Process Validation About Us Webinars SeminarsPast Seminar Pictures 2-day In-person SeminarApplied Statistics for FDA Process ValidationClick Here for More Details! Overview:In Guidance for Industry Process Validation: General Principle and Practices, process validation is defined as, ""...the collection and evaluation of data, from the process design stage through commercial production.." The guidance further delineates the 'process design stage through commercial production' into three distinct stages of the product lifecycle: Stage 1: Process Design: The commercial manufacturing process is defined during this stage based on knowledge gained through development and scale-up activities. Stage 2: Process Qualification: During this stage, the process design is evaluated to determine if the process is capable of reproducible commercial manufacturing. Stage 3: Continued Process Verification: Ongoing assurance is gained during routine production that the process remains in a state of control. Read more... Date & Time Date: May 17th & 18th, 2018 Time: 9:00 AM to 6:00 PMDownload Seminar Brochure VenuePhiladelphia, PA DoubleTree by Hilton Philadelphia Airport Download Registration form Heath Rushing Co-founder and Principal, Adsurgo Heath Rushing, is the cofounder of Adsurgo and author of the book Design and Analysis of Experiments by Douglas Montgomery: A Supplement for using JMP. Previously, he was the JMP and Six Sigma training manager at SAS. He led a team of nine technical professionals designing and delivering applied statistics and quality continuing education courses. Reserve your Seat Now! Enroll Now! Copyright © 2016 GlobalCompliancePanel. All Rights Reserved. . [...] Content analysis details: (1.2 points, 3.0 required) pts rule name description ---- ---------------------- -------------------------------------------------- 0.0 URIBL_BLOCKED ADMINISTRATOR NOTICE: The query to URIBL was blocked. See http://wiki.apache.org/spamassassin/DnsBlocklists#dnsbl-block for more information. [URIs: compliance4all.com] -0.0 SPF_PASS SPF: sender matches SPF record 0.2 HEADER_FROM_DIFFERENT_DOMAINS From and EnvelopeFrom 2nd level mail domains are different 0.0 HTML_MESSAGE BODY: HTML included in message 0.8 BAYES_50 BODY: Bayes spam probability is 40 to 60% [score: 0.4669] 0.2 KAM_TRACKIMAGE RAW: Message has a remote image explicitly meant for tracking -0.1 DKIM_VALID Message has at least one valid DKIM or DK signature 0.1 DKIM_SIGNED Message has a DKIM or DK signature, not necessarily valid -0.1 DKIM_VALID_AU Message has a valid DKIM or DK signature from author's domain 0.0 MSGID_FROM_MTA_HEADER Message-Id was added by a relay X-Spam-Flag: NO --_----------=_MCPart_901487339 Content-Type: text/plain; charset=utf-8 Content-Transfer-Encoding: quoted-printable Applied Statistics for FDA Process Validation About Us Webinars SeminarsPast Seminar Pictures=20 2-day In-person SeminarApplied Statistics for FDA Process ValidationClick = Here for More Details! Overview:In Guidance for Industry Process Validation: General Principle and= Practices, process validation is defined as, ""...the collection and = evaluation of data, from the process design stage through commercial = production.." The guidance further delineates the 'process design stage = through commercial production' into three distinct stages of the product = lifecycle: Stage 1: Process Design: The commercial manufacturing process is defined = during this stage based on knowledge gained through development and = scale-up activities. Stage 2: Process Qualification: During this stage, the process design is = evaluated to determine if the process is capable of reproducible commercial= manufacturing. Stage 3: Continued Process Verification: Ongoing assurance is gained during= routine production that the process remains in a state of control. Read = more... Date & Time Date: May 17th & 18th, 2018 Time: 9:00 AM to 6:00 PMDownload Seminar Brochure=20 VenuePhiladelphia, PA DoubleTree by Hilton Philadelphia Airport Download Registration form Heath Rushing=20 Co-founder and Principal, Adsurgo Heath Rushing, is the cofounder of = Adsurgo and author of the book Design and Analysis of Experiments by = Douglas Montgomery: A Supplement for using JMP. Previously, he was the JMP = and Six Sigma training manager at SAS. He led a team of nine technical = professionals designing and delivering applied statistics and quality = continuing education courses.=20 Reserve your Seat Now!=20 Enroll Now! Copyright =C2=A9 2016 GlobalCompliancePanel. All Rights Reserved.=20 . --_----------=_MCPart_901487339 Content-Type: text/html Content-Transfer-Encoding: quoted-printable
 
 
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About Us We= binars Seminars
Past Seminar Pictures
 
 
 
3D"top
 
 
2-day In-person Seminar
Applied Statistics for FDA Process Validation
Click Here for More Details!
 
 
3D"bottom
 
 
Overview:In Guidance for Industry Process = Validation: General Principle and Practices, process validation is defined = as, ""...the collection and evaluation of data, from the process = design stage through commercial production.." The guidance further = delineates the 'process design stage through commercial production'= into three distinct stages of the product lifecycle:

Stage 1: Process Design: The commercial manufacturing = process is defined during this stage based on knowledge gained through = development and scale-up activities.

Stage 2: Process Qualification: During this stage, the = process design is evaluated to determine if the process is capable of = reproducible commercial manufacturing.

Stage 3: Continued Process Verification: Ongoing assurance = is gained during routine production that the process remains in a state of = control. Read = more...
 
 
 
Date & Time
Date: May 17th & 18th, 2018
Time: 9:00 AM to 6:00 PM
Download Seminar Brochure
 
Venue
Philadelphia, PA
DoubleTree by Hilton Philadelphia Airport
Download Registration form
 
 
 
3D"img-160-160"
Heath Rushing
Co-founde= r and Principal, Adsurgo
Heath Rushing, is the cofounder of = Adsurgo and author of the book Design and Analysis of Experiments by= Douglas Montgomery: A Supplement for using JMP. Previously, he was the JMP= and Six Sigma training manager at SAS. He led a team of nine technical = professionals designing and delivering applied statistics and quality = continuing education courses.
 
 
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Reserve your Seat Now!
 
Enroll Now!
 
 
3D"bottom
 
 
Copyright © = 2016 GlobalCompliancePanel. All Rights Reserved.
 

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