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					<title>Latest Medical/Pharmaceuticals News and Press Release – Free Medical/Pharmaceuticals RSS @ 1888 Press Release.com</title> 
					<link>http://www.1888pressrelease.com</link> 
					<description>Free Medical/Pharmaceuticals RSS. Subscribe to latest Medical/Pharmaceuticals News and press releases @ 1888 PressRelease.Com.</description> 
					<copyright>(c) 2005-2013, 1888 Press Release.com. All rights reserved.</copyright><item>
								<title>2-day In-person Seminar on -Statistical Process Control for Process Development and Validation- at Philadelphia</title>
								<link>http://www.1888pressrelease.com/2-day-in-person-seminar-on-statistical-process-control-for-pr-468568.html</link> 
								<description>GlobalCompliancePanel to hold two-day, in-person seminar in Philadelphia on the topic, -Statistical Process Control for Process Development and Validation- on May 23 and 24, 2013 (Thursday and Friday). Steven Kuwahara, Founder and Principal, GXP Biotechnology LLC, will be the speaker at this two-day session.</description>				
								<pubDate>Thu, 23 May 2013 00:00:00 GMT</pubDate>
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								<title>CIS Addresses Key Sunshine Act Considerations and Operational Challenges at Upcoming Webinars and Conferences</title>
								<link>http://www.1888pressrelease.com/cis-addresses-key-sunshine-act-considerations-and-operationa-pr-472403.html</link> 
								<description>CIS will provide thought leadership at several industry-leading conferences and host four webinars to advance techniques that ensure -sunshine readiness- and identify potential operational challenges in preparation for CMS' federal transparency and disclosure collection that begins on August 1, 2013.</description>				
								<pubDate>Wed, 22 May 2013 00:00:00 GMT</pubDate>
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								<title>2-day In-person Seminar on -Software Validation for the New FDA Inspections- at Hotel Lalit, Mumbai</title>
								<link>http://www.1888pressrelease.com/2-day-in-person-seminar-on-software-validation-for-the-new-pr-470330.html</link> 
								<description>GlobalCompliancePanel to hold two-day, in-person seminar in Mumbai on the topic, -Software Validation for the New FDA Inspections- on July 1 and 2, 2013 (Monday and Tuesday). David Nettleton, an FDA Compliance Specialist for 21 CFR Part 11, HIPAA, and Computer System Validation, will be the speaker at this two-day session.</description>				
								<pubDate>Fri, 10 May 2013 00:00:00 GMT</pubDate>
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								<title>CIS Offers Initial Observations and a Webinar to Help Address Operational Challenges Related to CMS' Teaching Hospitals List</title>
								<link>http://www.1888pressrelease.com/cis-offers-initial-observations-and-a-webinar-to-help-addres-pr-470007.html</link> 
								<description>Compliance Implementation Services (CIS), a leading life sciences consulting firm, announced that on Friday, May 3, CMS published its list of Teaching Hospitals in conjunction with OPEN PAYMENTS, the CMS program under which applicable manufacturers and group purchasing organizations (GPOs) will begin tracking and reporting payments and other transfers of value to physicians and teaching hospitals.</description>				
								<pubDate>Wed, 08 May 2013 00:00:00 GMT</pubDate>
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								<title>Confluent Translations Takes Part in MAGI EAST 2013</title>
								<link>http://www.1888pressrelease.com/confluent-translations-takes-part-in-magi-east-2013-pr-468866.html</link> 
								<description>Nancy Cardone will contribute in discussions on global clinical research and new developments in investigator and subject recruiting internationally.</description>				
								<pubDate>Wed, 01 May 2013 00:00:00 GMT</pubDate>
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								<title>CIS to Speak at the West Coast Forum on Sunshine and Aggregate Spend and Assist Manufacturers with Sunshine Act Readiness Assessments</title>
								<link>http://www.1888pressrelease.com/cis-to-speak-at-the-west-coast-forum-on-sunshine-and-aggrega-pr-467845.html</link> 
								<description>Compliance Implementation Services (CIS), a leading life sciences consulting firm, today announced that Judy Fox, Director, Transparency Compliance and Adam Toronto, Associate Director, Commercial Compliance, will speak at the 4th Annual West Coast Forum on Sunshine and Aggregate Spend, taking place in San Diego on April 23-25. </description>				
								<pubDate>Thu, 25 Apr 2013 00:00:00 GMT</pubDate>
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								<title>Paragon Laboratories Launches Redesigned Website with New Free Tools for Supplement Marketers</title>
								<link>http://www.1888pressrelease.com/paragon-laboratories-launches-redesigned-website-with-new-fr-pr-467000.html</link> 
								<description>The new site design is user-friendly and provides a graphically-enhanced stroll through product showcases, nutrition news, health and wellness education, video features and Paragon Laboratories corporate highlights.</description>				
								<pubDate>Sat, 20 Apr 2013 00:00:00 GMT</pubDate>
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								<title>CIS Symposium Helps Medical Device Companies Understand Sunshine Act Compliance and Reporting Requirements</title>
								<link>http://www.1888pressrelease.com/cis-symposium-helps-medical-device-companies-understand-suns-pr-466666.html</link> 
								<description>The symposium -Sunshine - How to Weather the Storm of Federal and State Regulations,- held March 26 in Long Beach, featured a panel of industry experts from CIS and Advanced Orthopaedic Solutions (AOS) who discussed the key federal and state compliance and reporting requirements.</description>				
								<pubDate>Thu, 18 Apr 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -New EU Pharmacovigilance Directive and Regulations- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-new-eu-pharmacovigilance-direc-pr-464608.html</link> 
								<description>GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, -New EU Pharmacovigilance Directive and Regulations- on April 9. This 90-minute webinar earns up to 1.5 RAC credits towards a participant's RAC recertification upon full completion.</description>				
								<pubDate>Sat, 06 Apr 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -Statistics for Quality Control and Process Validation: Statistical Process Control (SPC) for Variable Data- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-statistics-for-quality-control-pr-464430.html</link> 
								<description>GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, -Statistics for Quality Control and Process Validation: Statistical Process Control (SPC) for Variable Data- on April 11. This webinar earns up to 1.5 RAC credits towards a participant's RAC recertification upon full completion.</description>				
								<pubDate>Fri, 05 Apr 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -Statistics for Quality Control and Process Validation: Statistical Process Control (SPC) for Attribute Data- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-statistics-for-quality-control-pr-464431.html</link> 
								<description>GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, -Statistics for Quality Control and Process Validation: Statistical Process Control (SPC) for Attribute Data- on April 11. This webinar earns up to 1.5 RAC credits towards a participant's RAC recertification upon full completion.</description>				
								<pubDate>Fri, 05 Apr 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -HACCP Training for Food Processing team members- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-haccp-training-for-food-proces-pr-462001.html</link> 
								<description>This course is about the Hazard Analysis and Critical Control Point (HACCP). It will introduce the role of the HACCP. It will start with a chronology of the HACCP program in the US food industry, in which it will cover important historical events and program milestones.</description>				
								<pubDate>Thu, 28 Mar 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs)- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-key-factors-to-write-an-effect-pr-462000.html</link> 
								<description>It is an irony of sorts that although companies that are regulated by the Code of Federal Regulations such as Title 21 and Title 493 are required by law to have Standard Operating Procedures (SOPs); there is no guidance on how to write, organize and maintain these critical guidance documents.</description>				
								<pubDate>Wed, 27 Mar 2013 00:00:00 GMT</pubDate>
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								<title>2-day In-person Seminar on Software Validation for the New FDA Inspections</title>
								<link>http://www.1888pressrelease.com/2-day-in-person-seminar-on-software-validation-for-the-new-f-pr-462576.html</link> 
								<description>GlobalCompliancePanel to hold two-day, in-person seminar in Philadelphia on the topic, -Software Validation for the New FDA Inspections- on April 18 and 19, 2013( Thursday and Friday). David Nettleton, an FDA Compliance Specialist for 21 CFR Part 11, HIPAA, and Computer System Validation, will be the speaker at this two-day session.</description>				
								<pubDate>Tue, 26 Mar 2013 00:00:00 GMT</pubDate>
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								<title>2-day In-person Seminar on Effective Complaint Handling, Medical Device Reporting and Recalls</title>
								<link>http://www.1888pressrelease.com/2-day-in-person-seminar-on-effective-complaint-handling-med-pr-462579.html</link> 
								<description>GlobalCompliancePanel to hold two-day, in-person seminar in San Francisco, CA on the topic, -Effective Complaint Handling, Medical Device Reporting and Recalls- on April 25 and 26, 2013 (Thursday and Friday). David R. Dills, a senior Regulatory and Compliance Consultant, will be the speaker at this two-day session.</description>				
								<pubDate>Tue, 26 Mar 2013 00:00:00 GMT</pubDate>
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								<title>CIS Medical Device Symposium Addresses Requirements of Federal Sunshine Act Regulations and Discusses Ongoing State Compliance and Reporting Requirements</title>
								<link>http://www.1888pressrelease.com/cis-medical-device-symposium-addresses-requirements-of-feder-pr-462712.html</link> 
								<description>Upcoming symposium is designed specifically for medical device companies interested in learning critical strategies to better manage federal and state compliance and reporting requirements.</description>				
								<pubDate>Tue, 26 Mar 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -Key Factors to develop an effective CAPA system- fromGlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-key-factors-to-develop-an-effe-pr-462292.html</link> 
								<description>GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on April 9, 2013.Kim Huynh-Ba, Executive Director of Pharmalytik will be the Speaker at this session, whose topic will be-Key Factors to develop an effective CAPA system-.</description>				
								<pubDate>Sat, 23 Mar 2013 00:00:00 GMT</pubDate>
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								<title>CIS Executive Symposium Reveals Important Commercialization Considerations for BayBio Members</title>
								<link>http://www.1888pressrelease.com/cis-executive-symposium-reveals-important-commercialization-pr-462357.html</link> 
								<description>Compliance Implementation Services (CIS), a leading life sciences consulting firm, recently hosted an executive breakfast for BayBio member companies and other executives in the life sciences community. </description>				
								<pubDate>Sat, 23 Mar 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -Keys to an Effective Technology Transfer as an Element of the Knowledge Management Requirements from ICH Q10-</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-keys-to-an-effective-technolog-pr-461341.html</link> 
								<description>-Keys to an Effective Technology Transfer as an Element of the Knowledge Management Requirements from ICH Q10- is the topic of a RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize on March 21.</description>				
								<pubDate>Thu, 21 Mar 2013 00:00:00 GMT</pubDate>
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								<title>GlobalCompliancePanel to organize RAPS pre-approved webinar on -Global Medical Device Adverse Event Reporting Systems in EU, Canada and US-</title>
								<link>http://www.1888pressrelease.com/globalcompliancepanel-to-organize-raps-pre-approved-webinar-pr-460572.html</link> 
								<description>GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on March 20 on the topic, -Global Medical Device Adverse Event Reporting Systems in EU, Canada and US-. Dr. David Lim, a certified RAC and Certified Quality Auditor (CQA), will be the speaker at this webinar.</description>				
								<pubDate>Wed, 20 Mar 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -Japan -Regulatory Filing Requirements and Compliance Processes for Life Sciences- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-japan-regulatory-filing-requi-pr-460574.html</link> 
								<description>GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, -Japan -Regulatory Filing Requirements and Compliance Processes for Life Sciences- on March 20.</description>				
								<pubDate>Wed, 20 Mar 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -Meet the U.S. FDA's Tougher Requirements for the 510(K)- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-meet-the-u-s-fda-s-tougher-re-pr-461340.html</link> 
								<description>-Meet the U.S. FDA's Tougher Requirements for the 510(K)- is the topic of a RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize on March 20.</description>				
								<pubDate>Wed, 20 Mar 2013 00:00:00 GMT</pubDate>
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								<title>GlobalCompliancePanel to organize RAPS pre-approved webinar on -Good Documentation Practices for GMP Operations-</title>
								<link>http://www.1888pressrelease.com/globalcompliancepanel-to-organize-raps-pre-approved-webinar-pr-460275.html</link> 
								<description>A RAPS pre-approved webinar on the topic, -Good Documentation Practices for GMP Operations- is being organized by GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, on March 19. This webinar earns up to 1.00 RAC credits towards a participant's RAC recertification upon full completion.</description>				
								<pubDate>Tue, 19 Mar 2013 00:00:00 GMT</pubDate>
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								<title>Growth in the Healthcare Industry Shifting from the Developed to the Emerging Markets</title>
								<link>http://www.1888pressrelease.com/growth-in-the-healthcare-industry-shifting-from-the-develope-pr-460479.html</link> 
								<description>Future growth in the developed healthcare markets is expected to be buffeted by a massive wave of patent expirations coupled by numerous cost constraining measures.</description>				
								<pubDate>Thu, 14 Mar 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -Project Management for Computer Systems Validation- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-project-management-for-compute-pr-459242.html</link> 
								<description>A RAPS pre-approved webinar on the topic, -Project Management for Computer Systems Validation- is being organized by GlobalCompliancePanel, a leading provider of regulatory and compliance continuing education training, on March 14.</description>				
								<pubDate>Wed, 13 Mar 2013 00:00:00 GMT</pubDate>
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								<title>GlobalCompliancePanel to organize RAPS pre-approved webinar on -Managing Your Medical Device Reporting (MDR)Program for Compliance Success-</title>
								<link>http://www.1888pressrelease.com/globalcompliancepanel-to-organize-raps-pre-approved-webinar-pr-459247.html</link> 
								<description>GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organizea RAPS pre-approved webinaron the topic, -Managing Your Medical Device Reporting (MDR) Program for Compliance Success-,on March 13.</description>				
								<pubDate>Wed, 13 Mar 2013 00:00:00 GMT</pubDate>
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								<title>New Study On Companion Diagnostics and Personalized Medicine Market Report 2012 By MarketResearchReports</title>
								<link>http://www.1888pressrelease.com/new-study-on-companion-diagnostics-and-personalized-medicine-pr-460033.html</link> 
								<description>New Market Research Report Added In MarketResearchReports.Biz Database Companion Diagnostics and Personalized Medicine Market Report 2012.</description>				
								<pubDate>Tue, 12 Mar 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -Medical Device Adverse Event Reporting Systems in EU, Canada and US- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-medical-device-adverse-event-r-pr-456182.html</link> 
								<description>-Medical Device Adverse Event Reporting Systems in EU, Canada and US- is the topic of a RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize on March 6. This webinar, a 60-minute session, earns 1.00 RAC credits towards a participant's RAC recertification upon full completion.</description>				
								<pubDate>Wed, 06 Mar 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -Disinfection and Clean room Cleaning in an FDA Regulated Environment-</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-disinfection-and-clean-room-cl-pr-456185.html</link> 
								<description>GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, -Disinfection and Clean room Cleaning in an FDA Regulated Environment- on March 5, 2013.</description>				
								<pubDate>Tue, 05 Mar 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -Complaint Handling in Compliance with FDA and ISO Regulations- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-complaint-handling-in-complian-pr-458659.html</link> 
								<description>GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, -Complaint Handling in Compliance with FDA and ISO Regulations- on March 5. This 60-minute webinar earns up to 1.0 RAC credits towards a participant's RAC recertification upon full completion.</description>				
								<pubDate>Tue, 05 Mar 2013 00:00:00 GMT</pubDate>
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								<title>Global Pharmaceutical Survey Market 2013-2014 Publishes By IndustryMonitor.co</title>
								<link>http://www.1888pressrelease.com/global-pharmaceutical-survey-market-2013-2014-publishes-by-i-pr-458850.html</link> 
								<description>IndustryMonitor.co Publishes Global Pharmaceutical Survey 2013-2014 - Market Trends, Buyer Spend and Procurement Strategies in the Global Pharmaceutical Industry.</description>				
								<pubDate>Tue, 05 Mar 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -Combination Products: FDA's Proposed Rule for GMP Requirements and Introduction and Expectations for 'Combo' Products- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-combination-products-fda-s-pr-pr-451962.html</link> 
								<description>-Combination products- is a broad term. The FDA describes it in fairly straightforward terms thus: -Combination products are therapeutic and diagnostic products that combine drugs, devices, and/or biological products.- Although simple in description, the complexity lies in the fact that there are very many combinations in the market, and they all have to be regulated.</description>				
								<pubDate>Thu, 28 Feb 2013 00:00:00 GMT</pubDate>
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								<title>New Research Report On Global Pharmacy Automation Market Analysis 2012-2016 By MarketResearchReports</title>
								<link>http://www.1888pressrelease.com/new-research-report-on-global-pharmacy-automation-market-ana-pr-456121.html</link> 
								<description>New Market Research Report Added In MarketResearchReports.Biz Database Global Pharmacy Automation Market 2012-2016.</description>				
								<pubDate>Wed, 20 Feb 2013 00:00:00 GMT</pubDate>
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								<title>GlobalCompliancePanel to organize RAPS pre-approved webinaron -Using Statistics to Determine Sample Size-</title>
								<link>http://www.1888pressrelease.com/globalcompliancepanel-to-organize-raps-pre-approved-webinaro-pr-453808.html</link> 
								<description>Steven Walfish, President of Statistical Outsourcing Services will be the Speaker ata RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organizeon February 19, 2013. It will be on the topic, -Using Statistics to Determine Sample Size- .</description>				
								<pubDate>Tue, 19 Feb 2013 00:00:00 GMT</pubDate>
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								<title>GlobalCompliancePanel to conduct RAPS pre-approved webinar on -Outsourcing Management -Effective Contract Manufacturers, Supplier Evaluation, Approval and Monitoring-</title>
								<link>http://www.1888pressrelease.com/globalcompliancepanel-to-conduct-raps-pre-approved-webinar-o-pr-454773.html</link> 
								<description>GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, -Outsourcing Management -Effective Contract Manufacturers, Supplier Evaluation, Approval and Monitoring-, on February 21. Miguel Montalvo, President of Expert Validation Consulting, will be the speaker at this 90-minute webinar.</description>				
								<pubDate>Sat, 16 Feb 2013 00:00:00 GMT</pubDate>
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								<title>The Larvol Group to Announce Free Online Pharma Platform - Larvol Sigma</title>
								<link>http://www.1888pressrelease.com/the-larvol-group-to-announce-free-online-pharma-platform-l-pr-455616.html</link> 
								<description>The Larvol Group, LLC announced today that it will provide a preview of its free pharmaceutical intelligence online platform, Larvol Sigma, on February 19th at the Pharma CI Conference in Zurich, Switzerland.</description>				
								<pubDate>Sat, 16 Feb 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -Implementing GAMP 5 in your Projects- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-implementing-gamp-5-in-your-pr-pr-452751.html</link> 
								<description>Good Automated Manufacturing Process (GAMP) 5 is a set of five important principles of automated manufacturing processes in the field of Life Sciences. Since it provides practical industry guidance on how to achieve compliant systems fit for intended use; it is considered the -how to- of a validated system in this industry.</description>				
								<pubDate>Fri, 15 Feb 2013 00:00:00 GMT</pubDate>
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								<title>India Seminar 2013 on -Good Laboratory Practice Regulations - Introduction and Strategies for Implementation- at Mumbai</title>
								<link>http://www.1888pressrelease.com/india-seminar-2013-on-good-laboratory-practice-regulations-pr-455104.html</link> 
								<description>GlobalCompliancePanel, a leading regulatory and compliance training gateway, will host a two-day, in-person seminar on the topic, -Good Laboratory Practice Regulations -Introduction and Strategies for Implementation- on March 21 and 22 at Mumbai, India.</description>				
								<pubDate>Fri, 15 Feb 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -Bullet Proof 510(k) - Latest FDA Proposed Changes to the Process- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-bullet-proof-510-k-latest-f-pr-453806.html</link> 
								<description>-Bullet Proof 510(k) - Latest FDA Proposed Changes to the Process- is the topic ofa RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize on February 13.</description>				
								<pubDate>Wed, 13 Feb 2013 00:00:00 GMT</pubDate>
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								<title>New Research Report On Over the counter(OTC) Pharmaceuticals Market in the Asia Pacific Region 2012-2016</title>
								<link>http://www.1888pressrelease.com/new-research-report-on-over-the-counter-otc-pharmaceuticals-pr-454838.html</link> 
								<description>New Market Research Report Added In MarketResearchReports.Biz Database Over the counter Pharmaceuticals Market in the Asia Pacific Region 2012-2016.</description>				
								<pubDate>Wed, 13 Feb 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -21 CFR Part 11 and Annex 11; What you Need to Know to Pass the New Regulatory Audits-</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-21-cfr-part-11-and-annex-11-w-pr-452750.html</link> 
								<description>In the course of his discussion, the presenter, David Nettleton will demystify Part 11 and the new European equivalent Annex 11. This session will put participants on the right track for using electronic records and signatures, which will help them to greatly increase productivity.</description>				
								<pubDate>Tue, 12 Feb 2013 00:00:00 GMT</pubDate>
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								<title>Design of Experiments and Statistical Process Control for Process Development and Validation From GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/design-of-experiments-and-statistical-process-control-for-pr-pr-447362.html</link> 
								<description>GlobalCompliancePanel, a leading regulatory and compliance training gateway, will host a two-day, in-person seminar on the topic, -Design of Experiments and Statistical Process Control for Process Development and Validation- on February 7 and 8 at Orange County, CA.</description>				
								<pubDate>Thu, 07 Feb 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -Scale-Up, Cycle Transfer, and Maximum Throughput Capability for Lyophilized Products- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-scale-up-cycle-transfer-and-pr-449825.html</link> 
								<description>Many problems have arisen in the past when designing and scaling-up lyophilization cycles because this process was subjective, being more of an art than a science, and cycles were designed and scaled-up based on a -trial and error- approach.</description>				
								<pubDate>Thu, 07 Feb 2013 00:00:00 GMT</pubDate>
							</item><item>
								<title>RAPS pre-approved webinar on -Clean room Design, Certification and Validation- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-clean-room-design-certificati-pr-452237.html</link> 
								<description>GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, -Clean room Design, Certification and Validation- on February 7, 2013. This 75-minute webinar earns up to 1.25 RAC credits towards a participant's RAC recertification upon full completion.</description>				
								<pubDate>Thu, 07 Feb 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -Adaptive Clinical Trials: The Modern Way of Doing Clinical Trials- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-adaptive-clinical-trials-the-pr-452238.html</link> 
								<description>Adaptive clinical trials, owing to their flexibility, help bring in the latest technological findings midway through into a clinical trial. This helps improve the end result quite dramatically.</description>				
								<pubDate>Wed, 06 Feb 2013 00:00:00 GMT</pubDate>
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								<title>RAPS pre-approved webinar on -510(K): Format and Contents- from GlobalCompliancePanel</title>
								<link>http://www.1888pressrelease.com/raps-pre-approved-webinar-on-510-k-format-and-contents-f-pr-452504.html</link> 
								<description>GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize RAPS pre-approved webinar on the topic, -510(K): Format and Contents-, on , February 6.Dr. David Lim, a certified RAC and Certified Quality Auditor (CQA), will be the speaker at this webinar, which earns up to 1.00 RAC credits towards a participant's RAC recertification upon completion.</description>				
								<pubDate>Tue, 05 Feb 2013 00:00:00 GMT</pubDate>
							</item><item>
								<title>Lupin Pharmaceuticals Begins Nationwide Rollout of POP's iPoint Mobile CRM for iPad</title>
								<link>http://www.1888pressrelease.com/lupin-pharmaceuticals-begins-nationwide-rollout-of-pop-s-ipo-pr-453035.html</link> 
								<description>iPoint Mobile CRM continues to be the first choice for pharmaceutical companies looking to put the iPad in the hands of their reps.  iPoint is the most customizable mobile CRM that meets PDMA compliance anywhere.</description>				
								<pubDate>Mon, 04 Feb 2013 00:00:00 GMT</pubDate>
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								<title>New Research Report On Global Cytomegalovirus Infections Market Analysis to 2019 By MarketResearchReports</title>
								<link>http://www.1888pressrelease.com/new-research-report-on-global-cytomegalovirus-infections-mar-pr-453022.html</link> 
								<description>New Market Research Report Added In MarketResearchReports.Biz Database Cytomegalovirus (CMV) Infections - Pipeline Assessment and Market Forecasts to 2019.</description>				
								<pubDate>Sat, 02 Feb 2013 00:00:00 GMT</pubDate>
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								<title>Confluent Translations to Exhibit at Cambridge Healthtech Institute's SCOPE Summit 2013</title>
								<link>http://www.1888pressrelease.com/confluent-translations-to-exhibit-at-cambridge-healthtech-in-pr-451178.html</link> 
								<description>Confluent Translations is excited to exhibit at the conference being held February 5-7, 2013. This is Cambridge Healthtech Institute's Fourth Annual Summit for Clinical Ops Executives, taking place in Miami, Florida.</description>				
								<pubDate>Thu, 24 Jan 2013 00:00:00 GMT</pubDate>
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								<title>2-day In-person Seminar on -Good Laboratory Practice Regulations - Introduction and Strategies for Implementation- at Mumbai</title>
								<link>http://www.1888pressrelease.com/2-day-in-person-seminar-on-good-laboratory-practice-regulat-pr-451252.html</link> 
								<description>GlobalCompliancePanel, a leading regulatory and compliance training gateway, will host a two-day, in-person seminar on the topic, -Good Laboratory Practice Regulations -Introduction and Strategies for Implementation- on March 21 and 22 at Mumbai, India.</description>				
								<pubDate>Thu, 24 Jan 2013 00:00:00 GMT</pubDate>
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