ISO

If you can't find what you want, Ask Us.

Refine Your Results

reset

Filter by Category

Location

Dates

FEATURED VENDORS

Showing 1-20 of 66 results Sort by:

Courses

  • 1 Request Info

    OHSAS 18001 – Occupational Health and Safety Management Systems – Lead Auditor Training in Dubai

    Lead Auditor Study.com is a platform that offers premium lead auditor courses, training and seminars to prepare students for various international certifications. we are located in Dubai and Qatar. BS OHSAS 18001:2007 Lead Auditor course in Dubai & Qatar is intended for Occupational Health and Safety (OHSAS) professionals intending to showcase their competence in Health and Safety Audits. OHSAS Lead Auditor course is also suitable for manager, supervisor, engineer or technician, involved in facility operation in compliance with OH&S regulations. The advantages of the OHSAS 18001:2007 Lead Auditor Course Once you become a certified OHSAS lead auditor you have the abilities to: Audit the processes and management system effectively Design the process and a procedure or a clause audit Prepare and plan audits in a risk-based manner Chose, lead and evaluate an audit team performances
  • 2 Request Info

    ISO 9001:2008 QMS Lead Auditor Course in Dubai & Qatar

    leadauditorstudy.com is a product of 3FOLD, we offers premium lead auditor courses, training and seminars to prepare students for various international certifications in Dubai & Qatar. we helped more than 12,000 students worldwide in their international certification needs. ISO 9001:2008 QMS Lead Auditor Course in Dubai & Qatar is intended for Quality Management System (QMS) auditors working for third-party certification bodies, registrars, and purchasing organization (second-party auditors). Quality management professionals such as consultants, quality managers, quality engineers, and employees conducting audits within their own organization (internal audits) will be immensely benefited from attending this course. With expert coaching and highly advance classroom technology, our institute is growing as a largest training centre in middle east for exam preparation. Further more details visit us http://www.leadauditorstudy.com/
  • 3 Request Info

    Understanding ISO 13485 and its Relation to FDA's Quality Systems Regulation by Jessica Czamanski

    Areas Covered in the Webinar: Concept of quality management system All clauses in ISO 13485 Auditable clauses of ISO 13485 All parts of the FDA’s QSR Who is responsible for complying with QSR Differences between ISO 13485 and QSR Role of management in quality Exclusions from specific parts of the regulation or standard Internal audit requirement Who Will Benefit: Medical device manufacturers R&D teams for medical devices Personnel involved in the packaging of medical devices and packaging engineers Inventory control personnel in a medical device company Quality personnel and quality engineers Suppliers to medical device companies Biomedical engineers Manufacturing engineers
  • 4 Request Info

    Washington Conference on Developing Documents and Records to meet the Requirement of ISO

    QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025:2005. The Quality System Manual (QSM) is the bible in a QMS environment because, much like its predecessor, Good Laboratory Practice (GLP), it contains the policies that the laboratory is expected to follow to achieve quality results. It is in fact only the "what to do" component of a QMS. What is also needed are the "how to do it" or procedures and methods and finally the controls or evidence that it was done properly.
  • 5 Request Info

    Developing Documents and Records to meet the Requirement of ISO

    QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025:2005. The Quality System Manual (QSM) is the bible in a QMS environment because, much like its predecessor, Good Laboratory Practice (GLP), it contains the policies that the laboratory is expected to follow to achieve quality results. It is in fact only the "what to do" component of a QMS. What is also needed are the "how to do it" or procedures and methods and finally the controls or evidence that it was done properly. GlobalCompliancePanel Refer a Friend Program: Any Customer to 3 Referrals "Can Participate 2 Days Seminar for free of Cost
  • 6 Request Info

    Complaints, Adverse Event Reporting, and Recalls - An Integrated Approach 2017

    Medical Device manufacturers operate in numerous regulatory systems that often have different requirements and are not always consistent. The new ISO 13485:2016 emphasizes this problem. Manufacturers must identify their roles, identify the regulatory requirements for that role, and incorporate them into the quality management system. The various jurisdictions, however, deal with post-market device issues in many different ways. The quality management system, QMS, needs three interlocking process: complaint management, adverse event reporting, and recalls. These processes also have supporting QMS processes such as corrective action and design changes. Overarching the QMS processes are the regulatory requirements, usually involving record keeping and reporting. This workshop covers these primary and secondary QMS processes and analyzes them in terms of US, EU, and Canadian regulations.
  • 7 Request Info

    Data Integrity, 21 CFR 11 & Annex 11 Implementation 2017

    The Problem: We have all heard of Data Integrity but do you really understand what it is? Do you understand how 21 CFR 11 and Annex 11 fit into this picture? Specifically, can you answer questions on the following: Evolution of 21 CFR Part 11 and Annex 11 and Why they are Back in the News Overview and Key Requirements of Part 11 & Annex 11 How to use a Risk Based Assessment to reduce work while still achieving Data Integrity and Compliance? How FDA & other Regulatory Authorities Inspect Computerized Systems for Data Integrity? I often refer to 21 CFR 11 and Annex 11 as Good Software Engineering with the Documentation on Steroids! However, unless one knows how to implement Data Integrity Read More: http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901052SEMINAR?trainingregistry-December-2017-SEO
  • 8 Request Info

    Implementing ISO 13485:2016

    The final version of ISO 13485:2016 is now available and companies should be planning their implementation. There are significant changes from the earlier version; they will require major modifications to the Quality Management System (QMS). The new version has better alignment with FDA's QSR, but there are still major differences that create issues for effective QMS implementation. This workshop covers the differences from the 2003 version to the 2016 version and offers practical implementation advice to update your QMS. Participants will also learn the differences with QSR and understand how to resolve them. The workshop uses extensive examples and exercises to help clarify the concerns. Click to Continue Reading: https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901429SEMINAR?trainingregistry-April-2018-SEO
  • 9 Request Info

    Webinar on ISO 13485:2016 - What's Changing and What It Means for Medical Device Companies

    This webinar focuses on what quality managers, quality system engineers, quality auditors and other personnel involved in quality system implementation will want to know about the upcoming revision and strategies of ISO 13485. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/ISO-13485-2016-501242/JAN-2016-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar on Monitoring and Measuring Customer Satisfaction Using ISO 10004:2012

    The ISO 10004:2012 model has four major elements in the customer satisfaction process: Identifying customer expectations, gathering data, analyzing the data, and communicating the information. The webinar explores each element and explains its application. The webinar also discusses the difference between a complaint in the regulatory realm and a complaint involving only customer satisfaction.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/CUSTOMER-SATISFACTION-MODELS-501278/MARCH-2016-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar on ISO 14971-Incorporating Risk Management throughout the Product Life-cycle

    A key process for all medical device companies is product risk management. While this webinar focuses on the application of risk management to product outlined in ISO 14971:2007, we will also discuss the risk-based approach outlined in ISO 13485:2016. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/ISO-14971-RISK-MGMT-501368/APRIL-2016-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar on New ISO Standard for Medical Device Quality Systems 13485: 2016 Summary of its Impact to the Medical Device Industry Professionals

    You will gain a thorough insight into the specific quality system requirements of all new International ISO 13485:2016 Quality System Standard requirements for Medical Devices. This timely and extremely informative webinar will truly build your knowledge from the fundamental quality principles. It will help you grow into fulfilling the quality and regulatory requirements as a professional working for medical device manufacturers of fully assembled devices and global suppliers manufacturing critical parts for the medical device industry. All noteworthy changes implemented into this key international standard will be discussed to pave the path for implementation of the changes in your organization. Price :- $250 Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/NEW-ISO-MEDICAL-DEVICES-501379/MAY-2016-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar On Validation of a HPLC/UPLC Methodology

    Instrumental liquid chromatography (HPLC method development/ UPLC method development) commonly used in the pharmaceutical, environmental, and other areas for analyses needs to comply with either Good Laboratory Practices or ISO 17025 training. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/VALIDATING-HPLC-METHODOLOGY-501397/MAY-2016-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar On Failure Mode and Effects Analysis

    Failure Mode Effects Analysis (FMEA) is a closed loop continuous improvement activity that begins by planning for quality. It identifies what can go wrong with a product or process, the severity and probability of the undesirable event, and existing controls (if any) to prevent or mitigate the problem. It is however not a once-and-done activity because it is updated to reflect actions taken to remove or mitigate failure modes.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/FAILURE-MODE-EFFECTS-ANALYSIS-501614/AUGUST-2016-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar On Meeting the Toughest Laboratory Accreditation Requirements (Part-2)

    Many laboratories regard Quality Assurance, Quality Assessment and Quality Control as independent activities, others use the terms interchangeably, e.g. QA/QC. This demonstrates a lack of appreciation of the differences between Assurance, Assessment and Control, as well as the interrelationships, particularly between QA and QC.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/TOUGHEST-LABORATORY-ACCREDITATION-501580/AUGUST-2016-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar On Setting and Measuring Quality Objectives

    The Quality Objectives, derived from the Quality Policy, must be measurable. Good metrics have characteristics that make them clear and understandable. This presentation describes three types of metrics, illustrates how to use them for the Quality Objectives, and provides examples developed using Excel. One of the metric types, related to cycle time, has a particularly interesting graph type available in Excel.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/SETTING-MEASURING-QUALITY-OBJECTIVES-501634/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 17 Request Info

    Two Days Workshop On Quality Management Systems that Comply with ISO13485:2016

    Quality Management Systems that Comply with ISO13485:2016" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.Price:$1400.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/workshop/Quality-Management-Systems-that-Comply-with-ISO13485-2016-800016/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar On ISO 37001-The New Anti-Bribery Management Systems Standard and its Impact: What does it mean for Global Small and Medium Businesses?

    The webinar will help your organization implement an anti-bribery management system, or enhance the controls you currently have to reduce the risk of bribery occurring and can demonstrate to your stakeholders that you have put in place internationally recognized good-practice anti-bribery controls. Bribery is one of the world's most destructive and challenging issues. With over US$ 1 trillion paid in bribes each year, the consequences are catastrophic, reducing quality of life, increasing poverty and eroding public trust.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/ISO-37001-ANTI-BRIBERY-MANAGEMENT-501912/DECEMBER-2016-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar On 21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration

    All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form of records. Medical device manufacturing plants, required to follow 21 CFR Part 820, have the additional responsibility to ensure that each and every step of the manufacturing process is controlled by work instructions, SOPs, set-up instructions, equipment maintenance, and support functions, and that evidence of this work is maintained by controlled records.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/21-CFR-PART-820-QUALITY-SYSTEM-501907/DECEMBER-2016-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar On Application of CMS Quality Indicator Process in Healthcare Food Service

    The Centers for Medicare & Medicaid Services (CMS), in collaboration with public and private partners, is transforming how they conduct business and operations, connect providers and empower consumers and their beneficiaries.CMS enhances its partnerships in a delivery system where providers are supported in achieving better outcomes in health and health care at lower cost for the beneficiaries and communities they serve.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/CMS-QUALITY-INDICATOR-501905/DECEMBER-2016-ES-TRAININGREGISTRY