Return-Path: Delivered-To: louk@transocean.com Received: from vps.transocean.com by vps.transocean.com with LMTP id cAWhOcVG11qTaQAAInt2oQ for ; Wed, 18 Apr 2018 06:23:17 -0700 Return-path: Envelope-to: louk@transocean.com Delivery-date: Wed, 18 Apr 2018 06:23:17 -0700 Received: from ccm38.constantcontact.com ([208.75.123.163]:43798) by vps.transocean.com with esmtps (TLSv1.2:ECDHE-RSA-AES256-GCM-SHA384:256) (Exim 4.89_1) (envelope-from ) id 1f8n39-00074Z-Iy for louk@transocean.com; Wed, 18 Apr 2018 06:23:17 -0700 Received: from [10.252.1.141] ([10.252.1.141:58838] helo=p2-jbemailsyndicator17.ctct.net) by 10.249.248.24 (envelope-from ) (ecelerity 4.2.1.52273 r(Core:4.2.1.11)) with ESMTP id 6E/72-26231-F8647DA5; Wed, 18 Apr 2018 09:22:23 -0400 DKIM-Signature: v=1; q=dns/txt; a=rsa-sha256; c=relaxed/relaxed; s=1000073432; d=auth.ccsend.com; h=date:mime-version:subject:X-Feedback-ID:message-id:from:reply-to:list-unsubscribe:list-unsubscribe-post:to; bh=oP6scuKRhNnpno1lrihCTF6yVvveKuuRbqyhqaiELoM=; b=HJeaAb3AKKzQva0PlFImM385OsFexMHdIHUwgoAHCUaPgEBJIYAOxBRGRIpN1+eE4gfkX/pgrWFu2P4t+T2uE4zBWZ+jxV+zjiNJ6auiCcHy4N/xK2DOmf63S10d41qORGtiVAcZ4ELEmhQI8fypcMSijBkLS7rQZoelKNJhA+c= Message-ID: <1130432391224.1130093494344.1598754893.0.400921JL.1002@scheduler.constantcontact.com> Date: Wed, 18 Apr 2018 09:22:23 -0400 (EDT) From: Jeff Kasoff Reply-To: info@ustrainings.com To: louk@transocean.com Subject: Qsr And Iso 13485 Requirements MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="----=_Part_636820451_1045698298.1524057743131" List-Unsubscribe: List-Unsubscribe-Post: List-Unsubscribe=One-Click X-Campaign-Activity-ID: ccb15c1e-8ffe-419f-a412-b3ae8a2456f9 X-Channel-ID: e24e8210-430a-11e8-b6fd-d4ae52754007 X-Mailer: Roving Constant Contact 2012 (http://www.constantcontact.com) X-Return-Path-Hint: AzLFcHo/+QZ+kErOuiiRW+Q==_1130093494344_4k6CEEMKEei2/dSuUnVABw==@in.constantcontact.com X-Roving-Campaignid: 1130432391224 X-Roving-Id: 1130093494344.1598754893 X-Feedback-ID: e24e8210-430a-11e8-b6fd-d4ae52754007:ccb15c1e-8ffe-419f-a412-b3ae8a2456f9:1130093494344:CTCT X-CTCT-ID: e0e3f590-430a-11e8-b6e2-d4ae52754007 X-Spam-Status: No, score=-5.2 X-Spam-Score: -51 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: Best practices for purchasing and supplier controls in the medical device industry Contact Us On: Phone: +1-(510)-868-1040 Email: info@ustrainings.com Best Practices For Purchasing And Supplier Controls In The Medical Device Industry Introduction: Supplier qualification and assessment is required in both the QSR regulations and ISO standards. Many companies spend a great deal of time and money in pursuit of compliance with this. Many companies can spend MUCH LESS time and money, and still be in control of their suppliers and in compliance with the regulations Why Should You Attend? This webinar will provide valuable assistance to all regulated companies that are interested in incurring less cost on supplier evaluation and assessment. Learning Objectives: QSR and ISO 13485 requirements for supplier selection and assessment How to qualify new suppliers in a cost efficient manner Learn More... Areas Covered In The Webinar:  How to assess current suppliers in a cost efficient manner How to perform supplier-related corrective action Learn More... Instructor Profile Jeff Kasoff Jeff Kasoff, RAC, CMQ/OE has more than 30 years in Quality and Regulatory management. Over that time, Jeff has implemented and overseen quality system operations and assured compliance, at all sizes of company, from startup to more than $100 million in revenue. Date: April 27, 2018 | Time: 01:00 PM EST | 10:00 AM PST | Duration: 90 Minutes Seats Are Getting Filled Hurry Up And Register Today!!! 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Many companies spend a great d= eal of time and money in pursuit of compliance with this. Many companies ca= n spend MUCH LESS time and money, and still be in control of their supplier= s and in compliance with the regulations Why Should You Attend? This webina= r will provide valuable assistance to all regulated companies that are inte= rested in incurring less cost on supplier evaluation and assessment. Learni= ng Objectives: QSR and ISO 13485 requirements for supplier selection and as= sessment How to qualify new suppliers in a cost efficient manner Learn More= ... Areas Covered In The Webinar: =EF=BB=BF How to assess current suppliers= in a cost efficient manner How to perform supplier-related corrective acti= on Learn More... Instructor Profile Jeff Kasoff Jeff Kasoff, RAC, CMQ/OE ha= s more than 30 years in Quality and Regulatory management. Over that time, = Jeff has implemented and overseen quality system operations and assured com= pliance, at all sizes of company, from startup to more than $100 million in= revenue. Date: April 27, 2018 | Time: 01:00 PM EST | 10:00 AM PST | Durati= on: 90 Minutes Seats Are Getting Filled Hurry Up And Register Today!!! N/A = | 230 Truxtun Ave, 5th floor, Bakersfield, CA 93301 Unsubscribe louk@transo= cean.com Update Profile | About our service provider Sent by info@ustrainin= gs.com in collaboration with Try it free today ------=_Part_636820451_1045698298.1524057743131 Content-Type: text/html; charset=utf-8 Content-Transfer-Encoding: quoted-printable
Best practices for purchasing and suppl= ier controls in the medical device industry
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Supplier qualification and assessment is required in both the QSR regula= tions and ISO standards. Many companies spend a great deal of time and mone= y in pursuit of compliance with this. Many companies can spend MUCH LESS ti= me and money, and still be in control of their suppliers and in compliance = with the regulations

This webinar will provide valuable assistance to all regulated = companies that are interested in incurring less cost on supplier evaluation= and assessment.
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  • QSR and ISO 13485 req= uirements for supplier selection and assessment
  • How to qualify new = suppliers in a cost efficient manner
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  • How to assess current suppliers in a cost efficie= nt manner
  • How to perform supplier-related corrective action

Jeff Kasoff, RAC, = CMQ/OE has more than 30 years in Quality and Regulatory management. Over th= at time, Jeff has implemented and overseen quality system operations and as= sured compliance, at all sizes of company, from startup to more than $100 m= illion in revenue.
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Date: April 27, 2018 | Time: 01:00 PM EST = | 10:00 AM PST | Duration: 90 Minutes
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=20 N/A | 230 Truxtun A= ve, 5th floor, Bakersfield= , CA 93301 =20
Unsubscribe louk@transocean.com
Update Profile | About our service provider
Sent by =20 info@ustrainings.com =20 =20 =20 in collaboration wi= th =20 =20
=20 =20
3D"Trusted
Try it free today
=20 =20
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