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  • 1 Request Info

    Workshop On Quality Management Systems that Comply with ISO13485:2016

    The medical device industry is in the midst of major change, with the publication of the FDA's UDI Regulation, the first revision in over a decade to the ISO 13485 Quality Management Systems standard, and the changes to the EU's Medical Device Regulation that was just approved in April 2017. All of these events have far-reaching effects on Quality Management Systems so it is critical to understand what has changed within ISO 13485:2016 in order to create a comprehensive quality plan for your organization to ensure continued compliance and certification.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/workshop/QUALITY-MANAGEMENT-ISO13485-2016-504371/JULY-2017-ES-TRAININGREGISTRY
  • 2 Request Info

    Webinar On Trends in Environmental, Health and Safety (EHS) rules, requirements; stay ahead of regulatory challenges

    TRENDS FOR THE ENVIRONMENT/EPA-- Over the years EPA has continued to create regulations; now approaching 90% of the almost 30,000 pages of federal regulatory requirements. This is not expected to continue. How the new president and his administration will affect regulations in place and in the pipeline is still unclear at this time.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/EHS-RULES-REGULATORY-CHALLENGES-502195/JUNE-2017-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar On Writing Effective Standard Operating Procedures and Work Instructions

    Standard Operating Procedures and Work Instructions - the documentation required by regulation - is essential to the effective and compliant running of any regulated business. Unfortunately, many individuals in those businesses miss the valuable opportunities that properly developed Standard Operating Procedures/Work Instructions can provide. Regulated documentation can serve a variety of purposes other than meeting a regulatory requirement - as training materials, to standardize operations, to manage individual and group performance, to identify the sources of deviations, etc. The key is to knowing how to write those documents to properly meet those needs.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/WRITING-EFFECTIVE-PROCEDURES-WORK-INSTRUCTIONS-509265/JUNE-2017-ES-TRAININGREGISTRY
  • 4 Request Info

    Webinar On ISO/IEC 17025:2017 Update: The New Standard for Laboratory Competence

    This course is a comprehensive review of the changes made to ISO/IEC 17025 during its recent revision. In this course, you will be guided through the impact to your existing ISO/IEC 17025 compliant system, as well as the necessary steps to ensure compliance to the new standard.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/ISO-IEC-17025-2017-UPDATE-LABORATORY-COMPETENCE-507671/JUNE-2017-ES-TRAININGREGISTRY
  • 5 Request Info

    Webinar On Elements of a Corrective and Preventive Action (CAPA) Program and Uses of CAPA Data

    Year after year, CAPA is the subsystem cited most frequently during FDA inspections. A robust Corrective and Preventive Action (CAPA) program is of the utmost importance to a medical device manufacturer. A system that identifies and eliminates non-conformances and potential non-conformances enables both regulatory compliance and cost savings. This session will discuss the importance, requirements, and elements of a CAPA program, as well as describing the uses of CAPA data. Application of risk management to your CAPA program will be discussed throughout the webinar.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/CAPA-PROGRAM-CAPA-DATA-505212/MAY-2017-ES-TRAININGREGISTRY
  • 6 Request Info

    Webinar On ISO 19011:2011-Guidelines for Auditing Management Systems to Conducting Effective Internal Audits

    This webinar will utilize ISO 19011:2011, ICH Q10 and FDA guidances and explain how to conduct an effective internal audit program. Attendees will learn the benefits of a well-designed and executed internal auditing program, an overview of various cGMP regulations and how to reinforce their quality system, along with potential efficiency enhancements.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-19011-2011-INTERNAL-AUDITS-505127/MAY-2017-ES-TRAININGREGISTRY
  • 7 Request Info

    Webinar On Medical Device Reporting Requirements for Manufacturers Final Guidance

    This webinar explains the MDR regulation considering the new information contained in the Guidance and describes a compliant MDR procedure. Areas covered will include death, injury and mal-function reporting requirements, record keeping requirements, report timing, clarification of the term ‘becoming aware’ and clarification of reporting using electronic form 3500A.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/FDA-MDR-REGULATION-506828/MAY-2017-ES-TRAININGREGISTRY
  • 8 Request Info

    Webinar On Test Method Validation to Verify your Device Performance

    This webinar will help you have an understanding of Test Method Validations to verify the performance of a Medical Device, global reference standards, the FDA requirements and how to perform successful TMV to ensure your inspection of verification is effective, using detailed real-life case studies.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/TEST-METHOD-MEDICAL-DEVICE-508490/MAY-2017-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar On Failure Mode and Effect Analysis (FMEA) – Risk Analysis and Management

    Failure Mode and Effects Analysis (FMEA) is a systematic method for preventing failure through the discovery and mitigation of potential failure modes and their cause mechanisms. Actions are developed in a team environment and address each high: severity, occurrence or detection ranking indicated by the analysis. Completed FMEA actions result in improved product performance, reduced warranty and increased product quality.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/FMEA-RISK-ANALYSIS-MANAGEMENT-508377/APRIL-2017-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar On Implementing a Change Control Quality System Successfully

    This web training session is designed to help attendees understand the fundamental change control steps and processes. The expert trainer will focus on change proposals, assessments, execution and final implementation of a change control quality system. The importance of proper planning, critical thinking skills, and co-ordination of all change activities will also be discussed.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/CONTROL-QUALITY-SYSTEM-508754/APRIL-2017-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar On Medical Records: Responding to Subpoenas and Investigations

    Learn how to respond to subpoenas and investigations while complying with HIPAA requirements, state law regulations and patients' privacy rights.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/MEDICAL-RECORDS-506966/APRIL-2017-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar On Thriving with the Revised ISO 14001 Standard; Key Changes and Transition Strategies

    The ISO 14001 standard has been updated. If you presently have the ISO 14001 standard in place at your facility this webinar is a must! The webinar will address the changes to the standard.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/THRIVING-REVISED-ISO-14001-502667/APRIL-2017-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar On Understanding Corrections and CA&PA;

    This presentation explains the differences as well the QMS requirements to help you understand, implement, and maintain the effective systems.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/UNDERSTANDING-CORRECTIONS-CA-PA-509049/APRIL-2017-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar On Auditing Information Security Using ISO 27001

    ISO 27001 describes how to manage information security in a company. According to its documentation, ISO 27001 was developed to "provide a model for establishing, implementing, operating, monitoring, reviewing, maintaining and improving an information security management system." By applying ISO 27001 standards effectively in your organization you can ensure a robust security for your organization's vital information assets.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/AUDITING-INFORMATION-SECURITY-ISO-27001-507735/MARCH-2017-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar On ISO 9001:2015 Transition Readiness: Not Too Early to Start

    ISO 9001:2015 contains a handful of significant changes from the 2008 standard and a quality management system (QMS) that meets the requirements of ISO 9001:2008 should already meet most of the new requirements. It is, however, not too early to begin the transition if this has not already been started. This presentation will discuss the new requirements, the necessary transition activities, and some tips that might make the transition easier.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-9001-2015-TRANSITION-READINESS-507891/MARCH-2017-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar On Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration

    Design controls involve the translation of user requirements (aka Voice of the Customer) into specific technical requirements as design inputs. These design inputs then form the basis of the design specification, which becomes the design output. Since design controls requires tracing backwards and forwards in order to link the requirements to their satisfaction, a problem faced by many companies is in having to maintain duplicate information across many controlled documents.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/DESIGN-INPUTS-OUTPUTS-TRACEABILITY-MATRIX-504902/MARCH-2017-ES-TRAININGREGISTRY
  • 17 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.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/ISO-37001-ANTI-BRIBERY-MANAGEMENET-501912/DECEMBER-2016-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar On Risk Management Using ISO 14971:2007 and EN ISO 14971:2012

    Risk management is essential to device design and required by other standards, such as usability engineering, biocompatibility and electrical safety. The basis is ISO 14971:2007, but many companies don't understand the standard, don't follow the process flow, and consequently don't have an effective implementation. This presentation helps you avoid the common problems and create a compliant system.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-14971-2007-501829/DECEMBER-2016-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar On Drive Continuous Improvement with Shingo Maps and ISO 9001:2015

    Shingo process maps were developed originally to support kaizen events and other improvement events. They can, however, support managed continual improvement along with ISO 9001:2015's requirement (7.5) for documented information; a common role of the traditional process flowchart.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/SHINGO-MAPS-ISO-9001-2015-501917/DECEMBER-2016-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar On Lean Healthcare Facility Design

    Everyone knows we must focus on safety in healthcare delivery. Attending this session will help you better understand how the built environment impacts safety and is integrated with operational efficiencies.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/LEAN-HEALTHCARE-FACILITY-DESIGN-501911/DECEMBER-2016-ES-TRAININGREGISTRY