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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: onlinecompliancepanel-webinar-mailer-SF-PETER-VISHTON-MAY03-EB http://click.news.onlinecompliancepanel-email.com/?qs=5c678685343f9ebfc0fe7e5d8a8cc75ab118ee5289b034b9033b68adaee8f26cc352a81af9f457e24d293c58b237f749 Pharma Water Systems - FDA Assurance of Validation Compliance LIVE WEBINAR Date: Thursday, 03 May 2018 Time: 11:30 AM PDT | 02:30 PM EDT [...] Content analysis details: (4.3 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: onlinecompliancepanel.com] 1.5 URIBL_RHS_DOB Contains an URI of a new domain (Day Old Bread) [URIs: onlinecompliancepanel-email.com] -0.0 SPF_PASS SPF: sender matches SPF record 0.0 HTML_MESSAGE BODY: HTML included in message 0.8 BAYES_50 BODY: Bayes spam probability is 40 to 60% [score: 0.5000] 0.0 HTML_FONT_LOW_CONTRAST BODY: HTML font color similar or identical to background 1.9 RAZOR2_CF_RANGE_51_100 Razor2 gives confidence level above 50% [cf: 100] 0.1 DKIM_SIGNED Message has a DKIM or DK signature, not necessarily valid 0.9 RAZOR2_CHECK Listed in Razor2 (http://razor.sf.net/) -0.1 DKIM_VALID_AU Message has a valid DKIM or DK signature from author's domain -0.1 DKIM_VALID Message has at least one valid DKIM or DK signature -1.0 MAILING_LIST_MULTI Multiple indicators imply a widely-seen list manager 0.2 KAM_LOTSOFHASH Emails with lots of hash-like gibberish X-Spam-Flag: YES Subject: ****SPAM**** Regulatory Standards for Pharmaceutical Water Systems This is a multi-part message in MIME format. --SwRdWbBYqiCM=_?: Content-Type: text/plain; charset="utf-8" Content-Transfer-Encoding: 8bit onlinecompliancepanel-webinar-mailer-SF-PETER-VISHTON-MAY03-EB http://click.news.onlinecompliancepanel-email.com/?qs=5c678685343f9ebfc0fe7e5d8a8cc75ab118ee5289b034b9033b68adaee8f26cc352a81af9f457e24d293c58b237f749 Pharma Water Systems - FDA Assurance of Validation Compliance LIVE WEBINAR Date: Thursday, 03 May 2018 Time: 11:30 AM PDT | 02:30 PM EDT http://click.news.onlinecompliancepanel-email.com/?qs=5c678685343f9ebfc0fe7e5d8a8cc75ab118ee5289b034b9033b68adaee8f26cc352a81af9f457e24d293c58b237f749 Call 510-857-5896 38780 Tyson Lane Suite 210 Fremont, CA-94536 Early Bird Offer! Use Promo Code RECD10 to Get 10% off on Recorded Session/CD/Flash Drive/Corporate Live Session/Super Combos of this webinar. Offer valid till April 22, 2018 midnight. Call us to know more. http://click.news.onlinecompliancepanel-email.com/?qs=5c678685343f9ebfc0fe7e5d8a8cc75ab118ee5289b034b9033b68adaee8f26cc352a81af9f457e24d293c58b237f749 http://click.news.onlinecompliancepanel-email.com/?qs=5c678685343f9ebfdf66e22631fa9bada3ef09f84355368cf07cdaa4df9965c46e98a0e80b0079a4f1f8e13e933cd7df mailto:customersupport@onlinecompliancepanel.com Water used in production processes for pharmaceutical products must meet stringent standards. Pharmaceutical Water is, perhaps, the most important of all pharmaceutical utilities. It is used as an incipient in many pharmaceutical formulations, as a cleaning agent and as separately packaged product diluents. All Pharma Manufacturing requires Pharma Water meeting FDA and Regulatory Standards. Pharma Drug manufacturing failing to meet Water Standards stops manufacturing until resolved. The FDA has developed their preferences how a Pharma Water System will be described, designed, manufactured, tested, commissioned and validated before placed into pharmaceutical product manufacturing. All steps require GMP Documentation. This presentation presents information that is required to accomplish a successful commissioning and validation of a Pharma Water System with minimum problems. Key Learning Objectives - Basic purified water and WFI systems production steps - Equipment that is commonly used to produce purified water and WFI - The basic regulatory standards for chemistry and biological levels of purified water and WFI - The STEPS required to meet FDA Commissioning and Validation of Pharma Water Systems to assure Compliance - Documentation required to meet FDA Commissioning and Validation of Pharma Water Systems - Examples of potential PROBLEMS that can cause a system to not meet FDA Compliance http://click.news.onlinecompliancepanel-email.com/?qs=5c678685343f9ebfc0fe7e5d8a8cc75ab118ee5289b034b9033b68adaee8f26cc352a81af9f457e24d293c58b237f749 View More http://click.news.onlinecompliancepanel-email.com/?qs=5c678685343f9ebf015139a3406eceaaa23711070f53a2c913e7a9cdae92b8f2d67e592545fde031ad51669b72b4bb3d http://click.news.onlinecompliancepanel-email.com/?qs=5c678685343f9ebfc0fe7e5d8a8cc75ab118ee5289b034b9033b68adaee8f26cc352a81af9f457e24d293c58b237f749 YES I am Attending http://click.news.onlinecompliancepanel-email.com/?qs=5c678685343f9ebf21e9995973010fd0322f452f827d4791ae7f36a69493d5f10b69ee9c86bfd2b01e90259e66ffbe66 NO I Want a Different Course http://click.news.onlinecompliancepanel-email.com/?qs=5c678685343f9ebfe76adb53fcc8fdc8217e2f73aad7db20ff2430001a9e13f5430697342494536bd9b907e40aeaa150 Peter T. Vishton, P.E. Peter is an Independent Pharmaceutical Water Systems Consultant supporting several companies. He completed his Bachelor's and Master's Degrees from Drexel University. He has 25 years of experience in Pharma including 10 years with Pharma Water Systems. His experience includes being a member of GMP Teams to Design / Construct / Start Up /Commission and Qualify new or expanded cGMP pharmaceutical facilities. Included were Production spaces, Manufacturing Equipment, Utilities and their Control Systems. Among the assignments were R&D, Parenterals, Biologics and OSD. http://click.news.onlinecompliancepanel-email.com/?qs=5c678685343f9ebfe76adb53fcc8fdc8217e2f73aad7db20ff2430001a9e13f5430697342494536bd9b907e40aeaa150 View More Similar On-Demand Webinar http://click.news.onlinecompliancepanel-email.com/?qs=5c678685343f9ebfc28264dc1885bbde31eb529da3edd0fdffbdf8ff7a27555ea7b50d6aa229736f14419774b0597d81 How to go Paperless in an FDA-Regulated Environment using Electronic Workflow Signature Approvals and Electronic Records http://click.news.onlinecompliancepanel-email.com/?qs=5c678685343f9ebf3ebe1cc4894c305d62c5bd4be48a89bb0b4677bb97e8875f1a7efb225705bbaab4258370637d5f58 View More http://click.news.onlinecompliancepanel-email.com/?qs=5c678685343f9ebfb422425b782c8171a5105d0764dcb3ca190f0b70f72f0e0893457516ca7b0fb906a225d84461e591 NEW! 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Pharma Water Systems - FDA Assurance of Validation Compliance
LIVE WEBINAR
Date: Thursday, 03 May 2018
Time: 11:30 AM PDT | 02:30 PM EDT
OCP_Logo
Call 510-857-5896
38780 Tyson Lane Suite 210 Fremont, CA-94536
Early Bird Offer! Use Promo Code RECD10 to Get 10% off on Recorded Session/CD/Flash Drive/
Corporate Live Session/Super Combos of this webinar. Offer valid till April 22, 2018 midnight. Call us to know more.
Water used in production processes for pharmaceutical products must meet stringent standards. Pharmaceutical Water is, perhaps, the most important of all pharmaceutical utilities. It is used as an incipient in many pharmaceutical formulations, as a cleaning agent and as separately packaged product diluents. All Pharma Manufacturing requires Pharma Water meeting FDA and Regulatory Standards. Pharma Drug manufacturing failing to meet Water Standards stops manufacturing until resolved. The FDA has developed their preferences how a Pharma Water System will be described, designed, manufactured, tested, commissioned and validated before placed into pharmaceutical product manufacturing. All steps require GMP Documentation. This presentation presents information that is required to accomplish a successful commissioning and validation of a Pharma Water System with minimum problems.

Key Learning Objectives
  • Basic purified water and WFI systems production steps
  • Equipment that is commonly used to produce purified water and WFI
  • The basic regulatory standards for chemistry and biological levels of purified water and WFI
  • The STEPS required to meet FDA Commissioning and Validation of Pharma Water Systems to assure Compliance
  • Documentation required to meet FDA Commissioning and Validation of Pharma Water Systems
  • Examples of potential PROBLEMS that can cause a system to not meet FDA Compliance
instructor Peter T. Vishton, P.E.
Peter is an Independent Pharmaceutical Water Systems Consultant supporting several companies. He completed his Bachelor's and Master's Degrees from Drexel University. He has 25 years of experience in Pharma including 10 years with Pharma Water Systems. His experience includes being a member of GMP Teams to Design / Construct / Start Up /Commission and Qualify new or expanded cGMP pharmaceutical facilities. Included were Production spaces, Manufacturing Equipment, Utilities and their Control Systems. Among the assignments were R&D, Parenterals, Biologics and OSD.
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