BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//PharmOut - ECPv6.16.5//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:PharmOut
X-ORIGINAL-URL:https://www.pharmout.net
X-WR-CALDESC:Events for PharmOut
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:Australia/Melbourne
BEGIN:STANDARD
TZOFFSETFROM:+1100
TZOFFSETTO:+1000
TZNAME:AEST
DTSTART:20250405T160000
END:STANDARD
BEGIN:DAYLIGHT
TZOFFSETFROM:+1000
TZOFFSETTO:+1100
TZNAME:AEDT
DTSTART:20251004T160000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:+1100
TZOFFSETTO:+1000
TZNAME:AEST
DTSTART:20260404T160000
END:STANDARD
BEGIN:DAYLIGHT
TZOFFSETFROM:+1000
TZOFFSETTO:+1100
TZNAME:AEDT
DTSTART:20261003T160000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:+1100
TZOFFSETTO:+1000
TZNAME:AEST
DTSTART:20270403T160000
END:STANDARD
BEGIN:DAYLIGHT
TZOFFSETFROM:+1000
TZOFFSETTO:+1100
TZNAME:AEDT
DTSTART:20271002T160000
END:DAYLIGHT
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20260708T090000
DTEND;TZID=Australia/Melbourne:20260708T160000
DTSTAMP:20260626T032440Z
CREATED:20260626T032440Z
LAST-MODIFIED:20260626T032440Z
UID:10000078-1783501200-1783526400@www.pharmout.net
SUMMARY:PIC/S GMP - Sydney
DESCRIPTION:We are offering a 1-day training course covering the essential “what you need to know” when it comes to GMP Part I Manufacturing Medicinal Products. Learn about the key requirements in each of the 9 chapters including the main inspection focus areas and how to avoid an audit finding.
URL:https://www.pharmout.net/course/pic-s-gmp-sydney/
LOCATION:Quest Macquarie Park\, 71 Epping Rd\, Sydney\, NSW\, 2113\, Australia
CATEGORIES:GMP
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2017/08/PICS-GMP-Training-Course-PE-009-13-1.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20260716T090000
DTEND;TZID=Australia/Melbourne:20260716T160000
DTSTAMP:20260511T015722Z
CREATED:20251110T024918Z
LAST-MODIFIED:20260511T015722Z
UID:10000054-1784192400-1784217600@www.pharmout.net
SUMMARY:Quality Risk Management ICH Q9 Workshop - Virtual
DESCRIPTION:This Quality Risk Management (QRM) course is focused on how the QRM regulations apply to everyday pharmaceutical and biotech manufacturing processes and to accurately assess the risk to product quality and patient safety. \nAs discussed at the International Council for Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use: \n“…the importance of quality systems has been recognized in the pharmaceutical industry\, and it is becoming evident that quality risk management is a valuable component of an effective quality system.”
URL:https://www.pharmout.net/course/quality-risk-management-ich-q9-workshop-virtual/
LOCATION:Virtual – MS Teams
CATEGORIES:QRM ICHQ9
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2018/07/iso13485.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20260728T090000
DTEND;TZID=Australia/Melbourne:20260728T160000
DTSTAMP:20260630T012942Z
CREATED:20250905T012749Z
LAST-MODIFIED:20260630T012942Z
UID:10000042-1785229200-1785254400@www.pharmout.net
SUMMARY:APVMA GMP - Virtual
DESCRIPTION:This course applies to manufacturers of veterinary medicinal products. Veterinary medicinal products are required to be fit for their intended use and not place treated animals or users at risk due to inadequate safety\, quality or efficacy. The manufacture of veterinary medicinal products must ensure their products meet their registration requirements and there is batch-to-batch consistency.
URL:https://www.pharmout.net/course/apvma-gmp-3/
LOCATION:Virtual – MS Teams
CATEGORIES:APVMA GMP
ATTACH;FMTTYPE=image/png:https://www.pharmout.net/wp-content/uploads/2025/09/AVPMA-GMP-training-workshop-veterinary-chemicals.png
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20260731T090000
DTEND;TZID=Australia/Melbourne:20260731T160000
DTSTAMP:20260623T221617Z
CREATED:20260623T221617Z
LAST-MODIFIED:20260623T221617Z
UID:10000077-1785488400-1785513600@www.pharmout.net
SUMMARY:Computer Systems Validation - Virtual
DESCRIPTION:PharmOut has been training on Computer Systems Validation since 2008\, much has changed recently\, surprisingly Data Integrity remains a hot topic with regulators. This course examines the latest GAMP 5 second edition\, including the new chapters on cloud storage\, Artificial Intelligence\, Machine Learning\, and Blockchain) as well as recent developments\, i.e. FDA’s draft Computer Software Assurance (CSA) Guideline\, and of course the PIC/S Data Integrity guidance PI041. Aside from shifts in regulations\, there have been significant technological shifts too\, as part of Pharma 4.0TM\, we have Software as a Medical Device (SaMD) and Software in a Medical Device. The computer systems validation course will cover both medical device and medicine regulations and recent challenges posed by emerging technologies like IoT’s. \nThe course provides a broad overview of the regulatory requirements for computerised systems and is designed for pharmaceutical and medical device professionals seeking training on a practical and cost-effective approach. We will cover the risk-based approach and a detailed overview of various CSV methodologies including those based on the ISPE Good Automated Manufacturing Practice (GAMP®5) guidance\, the waterfall and V models\, all meeting EU GMP & PIC/S PE 009 Annex 11 and the US FDA 21 CFR Parts 210\, 211\, 820 and 11. \n“There are major business benefits in having a defined process that delivers systems that are fit for intended use\, on time\, and within budget. Systems that are well defined and specified are easier to support and maintain\, resulting in less downtime and lower maintenance costs…” \nISPE GAMP® 5 “A Risk-Based Approach to Compliant GxP Computerized Systems”
URL:https://www.pharmout.net/course/computer-systems-validation-virtual-2/
LOCATION:Virtual – MS Teams
CATEGORIES:CSV
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2017/08/gamp5-csv-1.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20260806T090000
DTEND;TZID=Australia/Melbourne:20260806T160000
DTSTAMP:20260515T011807Z
CREATED:20260515T011807Z
LAST-MODIFIED:20260515T011807Z
UID:10000070-1786006800-1786032000@www.pharmout.net
SUMMARY:PIC/S GMP - Virtual
DESCRIPTION:We are offering a 1-day training course covering the essential “what you need to know” when it comes to GMP Part I Manufacturing Medicinal Products. Learn about the key requirements in each of the 9 chapters including the main inspection focus areas and how to avoid an audit finding.
URL:https://www.pharmout.net/course/pic-s-gmp-virtual/
LOCATION:Virtual – MS Teams
CATEGORIES:GMP
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2017/08/PICS-GMP-Training-Course-PE-009-13-1.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20260813T090000
DTEND;TZID=Australia/Melbourne:20260813T160000
DTSTAMP:20260601T005314Z
CREATED:20251110T005459Z
LAST-MODIFIED:20260601T005314Z
UID:10000053-1786611600-1786636800@www.pharmout.net
SUMMARY:Quality Management Systems ISO 13485 - Virtual
DESCRIPTION:This one-day ISO 13485 workshop covers the requirements of ISO 13485 and its implications within a medical device manufacturing company. PharmOut’s consultants regularly design and write Quality Management Systems for companies\, from the smallest to the large blue-chip companies. They have many practical suggestions on how to apply the ISO 13485 standard and with ready access to an ex\, TGA inspectors can answer the more difficult questions too. \nAs the ISO Standard 13485:2016 Medical Devices states: \n“All requirements of this International Standard are specific to organizations providing medical devices\, regardless of the type or size of the organization.”
URL:https://www.pharmout.net/course/quality-management-systems-iso-13485-2/
LOCATION:Virtual – MS Teams
CATEGORIES:QMS ISO 13485
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2018/07/iso13485.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20260818T090000
DTEND;TZID=Australia/Melbourne:20260818T160000
DTSTAMP:20260511T015800Z
CREATED:20260416T051408Z
LAST-MODIFIED:20260511T015800Z
UID:10000067-1787043600-1787068800@www.pharmout.net
SUMMARY:Auditor - Virtual
DESCRIPTION:This Auditor Training Course is designed to provide participants with detailed knowledge of self-inspection or external auditing best practices. This course will help you to understand how and why you need to monitor your GMP systems and how to identify\, record and address necessary corrective actions and continuous improvement items as part of your internal or external audit program. \n\n\n\n\n\n\n\n\n\n\n 
URL:https://www.pharmout.net/course/auditor-2/
LOCATION:Virtual – MS Teams
CATEGORIES:Auditor
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2017/08/Self-Inspection-internal-audit-Training-1.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20260820T110000
DTEND;TZID=Australia/Melbourne:20260820T150000
DTSTAMP:20260511T020019Z
CREATED:20260312T045213Z
LAST-MODIFIED:20260511T020019Z
UID:10000063-1787223600-1787238000@www.pharmout.net
SUMMARY:Audit Preparation Workshop - Virtual
DESCRIPTION:This Audit Preparation Training Course is designed to provide participants with detailed knowledge of the external audit process and the roles and responsibilities of an auditee. \nThis course will help you to understand how to prepare your work environment\, what to expect on the day of the audit (both onsite and remote audits)\, what auditors will ask for or look for\, and how to respond to audit findings. \nIt will help take the stress and anxiety out of an upcoming audit and leave you feeling ready for the audit day.
URL:https://www.pharmout.net/course/audit-preparation-workshop-virtual-2/
LOCATION:Virtual – MS Teams
CATEGORIES:Audit Preparation
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2017/08/Self-Inspection-internal-audit-Training-1.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20260910T090000
DTEND;TZID=Australia/Melbourne:20260910T160000
DTSTAMP:20260626T042144Z
CREATED:20260626T042144Z
LAST-MODIFIED:20260626T042144Z
UID:10000079-1789030800-1789056000@www.pharmout.net
SUMMARY:GMP Code: Blood and Tissue Products (TGA Regulations) - Virtual
DESCRIPTION:This course applies to manufacturers that undertake the collection\, processing\, testing\, storage\, release for supply\, and quality assurance of Human Blood and Blood Components\, Human Tissues and Human Cellular Therapy Products.  The purpose of this workshop is to provide participants with an understanding of the Australian Code of GMP for human blood and blood components\, human tissues and human cellular therapy products.  The training is based on Version 1.0 April 2013 and TGO 108 requirements.  It also includes any latest guidance and GMP focus areas.
URL:https://www.pharmout.net/course/gmp-code-blood-and-tissue-products-tga-regulations-virtual/
LOCATION:Virtual – MS Teams
CATEGORIES:GMP
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2021/04/APVMA-GMP-Training-Australian-code-of-GMP-v2.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20260916T090000
DTEND;TZID=Australia/Melbourne:20260916T160000
DTSTAMP:20260615T051751Z
CREATED:20251110T003939Z
LAST-MODIFIED:20260615T051751Z
UID:10000051-1789549200-1789574400@www.pharmout.net
SUMMARY:CAPA - Brisbane
DESCRIPTION:This CAPA Workshop is designed to provide you with an overview of a typical Corrective Action and Preventive Action (CAPA) program to handle outputs as part of a Pharmaceutical Quality System (PQS). \nThis course will help you to understand how to run an effective CAPA process and use it for continuous improvement.
URL:https://www.pharmout.net/course/capa-brisbane/
LOCATION:Hotel Amora Brisbane\, 200 Creek St\, Brisbane\, QLD\, 4000\, Australia
CATEGORIES:CAPA
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2018/07/capa2.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20261001T090000
DTEND;TZID=Australia/Melbourne:20261001T160000
DTSTAMP:20260622T052801Z
CREATED:20260109T004648Z
LAST-MODIFIED:20260622T052801Z
UID:10000058-1790845200-1790870400@www.pharmout.net
SUMMARY:PIC/S GMP - Sydney
DESCRIPTION:We are offering a 1-day training course covering the essential “what you need to know” when it comes to GMP Part I Manufacturing Medicinal Products. Learn about the key requirements in each of the 9 chapters including the main inspection focus areas and how to avoid an audit finding.
URL:https://www.pharmout.net/course/gmp-sydney/
LOCATION:Quest Macquarie Park\, 71 Epping Rd\, Sydney\, NSW\, 2113\, Australia
CATEGORIES:GMP
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2017/08/PICS-GMP-Training-Course-PE-009-13-1.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20261008T090000
DTEND;TZID=Australia/Melbourne:20261008T160000
DTSTAMP:20260511T015818Z
CREATED:20260301T222228Z
LAST-MODIFIED:20260511T015818Z
UID:10000061-1791450000-1791475200@www.pharmout.net
SUMMARY:APVMA GMP - Virtual
DESCRIPTION:This course applies to manufacturers of veterinary medicinal products. Veterinary medicinal products are required to be fit for their intended use and not place treated animals or users at risk due to inadequate safety\, quality or efficacy. The manufacture of veterinary medicinal products must ensure their products meet their registration requirements and there is batch-to-batch consistency.
URL:https://www.pharmout.net/course/apvma-gmp/
LOCATION:Virtual – MS Teams
CATEGORIES:APVMA GMP
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2021/04/APVMA-GMP-Training-Australian-code-of-GMP-v2.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20261013T090000
DTEND;TZID=Australia/Melbourne:20261013T160000
DTSTAMP:20260526T030054Z
CREATED:20260526T030054Z
LAST-MODIFIED:20260526T030054Z
UID:10000071-1791882000-1791907200@www.pharmout.net
SUMMARY:Validation - Virtual
DESCRIPTION:This one-day Validation training workshop is designed to provide an overview of the current concepts and guidance documents for Validation as defined by the US FDA in 2011 and PIC/S Annex 15 Qualification and Validation. The aim of the course is to provide practical insights into how validation is carried out and avoid common and costly mistakes. \nThe US FDA and EMA have slightly different approaches to Validation. Understanding these approaches will provide your team with the best opportunity to develop and implement your own compliant validation approaches\, and of course manufacture or deliver safe products for your customers. \n 
URL:https://www.pharmout.net/course/validation-virtual/
LOCATION:Virtual – MS Teams
CATEGORIES:GMP
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2017/08/PICS-GMP-Training-Course-PE-009-13-1.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20261015T090000
DTEND;TZID=Australia/Melbourne:20261015T160000
DTSTAMP:20260526T034432Z
CREATED:20260526T034432Z
LAST-MODIFIED:20260526T034432Z
UID:10000073-1792054800-1792080000@www.pharmout.net
SUMMARY:Computer Systems Validation - Virtual
DESCRIPTION:PharmOut has been training on Computer Systems Validation since 2008\, much has changed recently\, surprisingly Data Integrity remains a hot topic with regulators. This course examines the latest GAMP 5 second edition\, including the new chapters on cloud storage\, Artificial Intelligence\, Machine Learning\, and Blockchain) as well as recent developments\, i.e. FDA’s draft Computer Software Assurance (CSA) Guideline\, and of course the PIC/S Data Integrity guidance PI041. Aside from shifts in regulations\, there have been significant technological shifts too\, as part of Pharma 4.0TM\, we have Software as a Medical Device (SaMD) and Software in a Medical Device. The computer systems validation course will cover both medical device and medicine regulations and recent challenges posed by emerging technologies like IoT’s. \nThe course provides a broad overview of the regulatory requirements for computerised systems and is designed for pharmaceutical and medical device professionals seeking training on a practical and cost-effective approach. We will cover the risk-based approach and a detailed overview of various CSV methodologies including those based on the ISPE Good Automated Manufacturing Practice (GAMP®5) guidance\, the waterfall and V models\, all meeting EU GMP & PIC/S PE 009 Annex 11 and the US FDA 21 CFR Parts 210\, 211\, 820 and 11. \n“There are major business benefits in having a defined process that delivers systems that are fit for intended use\, on time\, and within budget. Systems that are well defined and specified are easier to support and maintain\, resulting in less downtime and lower maintenance costs…” \nISPE GAMP® 5 “A Risk-Based Approach to Compliant GxP Computerized Systems”
URL:https://www.pharmout.net/course/computer-systems-validation-virtual/
LOCATION:Virtual – MS Teams
CATEGORIES:CSV
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2017/08/gamp5-csv-1.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20261022T090000
DTEND;TZID=Australia/Melbourne:20261022T160000
DTSTAMP:20260526T034034Z
CREATED:20260526T034034Z
LAST-MODIFIED:20260526T034034Z
UID:10000072-1792659600-1792684800@www.pharmout.net
SUMMARY:CAPA - Virtual
DESCRIPTION:This CAPA Workshop is designed to provide you with an overview of a typical Corrective Action and Preventive Action (CAPA) program to handle outputs as part of a Pharmaceutical Quality System (PQS). \nThis course will help you to understand how to run an effective CAPA process and use it for continuous improvement.
URL:https://www.pharmout.net/course/capa-virtual/
LOCATION:Virtual – MS Teams
CATEGORIES:CAPA
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2018/07/capa2.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20261029T090000
DTEND;TZID=Australia/Melbourne:20261029T160000
DTSTAMP:20260609T231010Z
CREATED:20251109T232919Z
LAST-MODIFIED:20260609T231010Z
UID:10000049-1793264400-1793289600@www.pharmout.net
SUMMARY:PIC/S GMP - Melbourne
DESCRIPTION:We are offering a 1-day training course covering the essential “what you need to know” when it comes to GMP Part I Manufacturing Medicinal Products. Learn about the key requirements in each of the 9 chapters including the main inspection focus areas and how to avoid an audit finding.
URL:https://www.pharmout.net/course/gmp-melbourne/
LOCATION:The Manningham Hotel & Club\, 1 Thompsons Rd\, Bulleen\, Victoria\, 3105\, Australia
CATEGORIES:GMP
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2017/08/PICS-GMP-Training-Course-PE-009-13-1.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20261112T090000
DTEND;TZID=Australia/Melbourne:20261112T160000
DTSTAMP:20260511T015834Z
CREATED:20260301T222559Z
LAST-MODIFIED:20260511T015834Z
UID:10000062-1794474000-1794499200@www.pharmout.net
SUMMARY:Quality Management Systems ISO 13485 - Virtual
DESCRIPTION:This one-day ISO 13485 workshop covers the requirements of ISO 13485 and its implications within a medical device manufacturing company. PharmOut’s consultants regularly design and write Quality Management Systems for companies\, from the smallest to the large blue-chip companies. They have many practical suggestions on how to apply the ISO 13485 standard and with ready access to an ex\, TGA inspectors can answer the more difficult questions too. \nAs the ISO Standard 13485:2016 Medical Devices states: \n“All requirements of this International Standard are specific to organizations providing medical devices\, regardless of the type or size of the organization.”
URL:https://www.pharmout.net/course/quality-management-systems-iso-13485/
LOCATION:Virtual – MS Teams
CATEGORIES:QMS ISO 13485
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2018/07/iso13485.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20261117T090000
DTEND;TZID=Australia/Melbourne:20261117T160000
DTSTAMP:20260511T015847Z
CREATED:20260421T221910Z
LAST-MODIFIED:20260511T015847Z
UID:10000068-1794906000-1794931200@www.pharmout.net
SUMMARY:Good Distribution Practice - Virtual
DESCRIPTION:This Good Distribution Practice (GDP) Training is designed to cover the latest GDP requirements in the distribution and/or warehousing of Active Pharmaceutical Ingredients (API) and medicinal products. It covers the current GDP guidelines and incorporates GMP updates which contain specific GDP clauses – linking responsibilities between manufacturers and distributors of medicinal products. \nThe Good Distribution Practice Training Course will help you understand the importance of correctly managing an integrated supply chain. Distribution networks are becoming more and more complex and involve multiple parties. We will help you to identify the appropriate tools to assist you. GDP guidance is in place to prevent falsified medicines from entering the supply chain and also to maintain control of the distribution processes\, ensuring the quality and integrity of medicinal products.
URL:https://www.pharmout.net/course/good-distribution-practice/
LOCATION:Virtual – MS Teams
CATEGORIES:GDP
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2018/09/Good-Distribution-Practice.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20261119T090000
DTEND;TZID=Australia/Melbourne:20261119T160000
DTSTAMP:20260511T015905Z
CREATED:20251109T232511Z
LAST-MODIFIED:20260511T015905Z
UID:10000048-1795078800-1795104000@www.pharmout.net
SUMMARY:Quality Risk Management ISO 14971 Workshop - Virtual
DESCRIPTION:This introductory one-day workshop will cover the key concepts of ISO 14971 and how to apply the standard to the medical devices industry.
URL:https://www.pharmout.net/course/quality-risk-management-iso-14971-workshop/
LOCATION:Virtual – MS Teams
CATEGORIES:QRM ISO 14971
ATTACH;FMTTYPE=image/jpeg:https://www.pharmout.net/wp-content/uploads/2018/07/iso13485.jpg
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Australia/Melbourne:20261201T090000
DTEND;TZID=Australia/Melbourne:20261201T160000
DTSTAMP:20260610T051235Z
CREATED:20260610T051235Z
LAST-MODIFIED:20260610T051235Z
UID:10000075-1796115600-1796140800@www.pharmout.net
SUMMARY:SOP Technical Writing - Virtual
DESCRIPTION:Well written technical SOPs help employees understand information the first time they read or hear it. Who doesn’t want to improve compliance\, shorten induction time and reduce deviations caused by confusing procedures? \nIf you are asked to write SOPs as part of your job role\, would you like some straightforward guidance on where to start and how to write?\nIf so\, this SOP Technical Writing course is for you.
URL:https://www.pharmout.net/course/sop-technical-writing-virtual/
LOCATION:Virtual – MS Teams
CATEGORIES:Technical Writing
ORGANIZER;CN="PharmOut":MAILTO:info@pharmout.net
END:VEVENT
END:VCALENDAR