Process Management

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Courses

  • 1 Request Info

    Webinar On Implementing a Metrics Program - Uncovering and Overcoming the Challenges

    Recently the FDA released their draft guidance for industry entitled "Request for Quality Metrics". Much discussion of quality metrics has ensued regarding this guidance and its elements. This presentation provides an integrated view of the aspects of Quality Metrics including the required supporting quality culture..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/METRICS-PROGRAM-503090/AUGUST-2017-ES-TRAININGREGISTRY
  • 2 Request Info

    Webinar On Top Process Validation Mistakes - And How to Avoid Them

    Validation is an important element of the Quality System Regulations and ISO13485. This course will cover the essentials of validation. You’ll learn about what processes needed to be validated and what steps you need to take to validate processes. You’ll learn the essentials of validation planning, protocol writing, and change management. We’ll cover the steps of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) including tips and best practices. We’ll discuss the top mistakes that companies make and how you can avoid them..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/TOP-PROCESS-VALIDATION-MISTAKES-509627/AUGUST-2017-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar On Ensure Compliance to FDA's Design Control by using Requirements Management Techniques

    This webinar on FDA's design control requirements will discuss how a requirements management approach consistent with the CMMi requirements management KPA, helps companies meet FDA's design control requirements.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/COMPLIANCE-FDAs-DESIGN-CONTROL-504040/AUGUST-2017-ES-TRAININGREGISTRY
  • 4 Request Info

    LEAN SIX SIGMA YELLOW BELT CERT.

    Certification from Thayer School of Engineering at Dartmouth College; this workshop is for non-engineers that want to learn the basics of lean and six sigma process improvement and problem solving.
  • 5 Request Info

    "LEAN SIX SIGMA BLACK BELT CERT"

    Thayer School of Engineering at Dartmouth College Certification LSS Black Belt Training – (twenty 4-hour sessions) • Lean Six Sigma Black Belt workshop, LIVE (instructor-led) online sessions 8:30 am to 12:30 pm Eastern U.S. Time (2 session per week for 10 weeks) for a total of 10 days. • Certification from Thayer School of Engineering at Dartmouth upon successful completion of all requirements Note: All sessions are recorded for download to your computer in the event you miss a session or for review purposes
  • 6 Request Info

    Webinar On Conducting a Software Validation of Medical Device to Meet FDA Requirements

    This course will teach how to conduct a software validation program that will satisfy FDA requirements and produce a safe product. We will explain the role of risk analysis in validation. How software requirements are used in validation will be described. This course is not a programming course. We will discuss what must be done but will not discuss methods to execute necessary testing.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/SOFTWARE-VALIDATION-MEDICAL-DEVICE-501884/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 7 Request Info

    Webinar On Quality Metrics Program: FDA Challenges and Requirements including the New 'Quality Metrics Technical Conformation Guide' Released June 201

    The Food, Drug and Cosmetic Act of 1938 as revised by the Food and Drug Administration Safety and Innovation Act (FDASIA) of 2014, gives the FDA the authority to require the reporting of Quality Metrics. In July 2015 the FDA issued a draft guidance, 'Request for Quality Metrics' in which the Agency shared its plan to require all firms that market a drug substance or drug product in the U.S. to provide specific data to the FDA which it will use to calculate defined quality metrics.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/QUALITY-METRICS-PROGRAM-501727/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 8 Request Info

    Webinar On How to use Risk Based Process Safety's skills to be in compliance with ICH-Q9 "Quality Risk Management" in the Pharmaceutical Industry

    This webinar will cover the similarities between the second pillar "Knowing the Process" of the Risk Based Process Safety Management and ICH-Q9 "Quality Risk Analysis". This webinar will provide the tools and help to identify the process required information to perform the quality risk by using methodologies in the process hazard analysis (PHA) to determine possible deviation during the process to achieve the good quality of the finished product.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/QUALITY-RISK-MANAGEMENT-PHARMACEUTICAL-INDUSTRY-501651/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar On Risk Based Approach for Medical Device Design Control

    This course will explain how to manage a Design Control program that will meet FDA requirements and minimize chances of your medical device being recalled. Such a program will also help to get projects completed on time and within budget. The important and confusing question of when, in a development process, Design Control begins will be answered. The difference between pre-release and post release change control will be explained.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/RISK-BASED-APPROACH-MEDICAL-DEVICE-DESIGN-501511/AUGUST-2016-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar On Enhancing your CAPA Program by Developing a Learning Organization

    This Webinar provides tools needed to sell a meaningful CAPA program up to Management, by discussing how CAPA can be used as a tool to yield business results. This well-researched webinar references classic business literature, written by famous business minds, such as Peter Drucker and Peter Senge, to describe how a CAPA program appeals to the needs of Knowledge Workers in a Learning Organization, CAPA therefore becomes a business tool to un-learn behaviors that are thwarting progress in the organization, and becomes a tool for sustainable change, organization alignment and business risk management.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/ENHANCING-CAPA-PROGRAM-LEARNING-ORGANIZATON-501459/JUNE-2016-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar OGMPs for OTC and Cosmetic Products - US and Global Requirementsn

    The cosmetic good manufacturing practice is a set of manufacturing guidelines to ensure the safety and quality of cosmetic products. OTC drug manufacturers, labelers, packagers and holders must comply with good manufacturing practices.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/GMPS-OTC-COSMETIC-PRODUCTS-501385/MAY-2016-ES-TRAININGREGISTRY
  • 12 Request Info

    Heating, Ventilation, and Air Conditioning (HVAC) in a Regulated Environment

    This is a three-day course designed to provide individuals with an in depth understanding of the design, balancing, commissioning, operation and maintenance of HVAC systems in a regulated environment. The course consists of lectures and imbedded exercises. Participants will also be placed in several real life situations such as completing a compliance review of floor plans and air flow diagrams, room pressurization schemes, ductwork design, and air balance reports; conducting emergency egress analysis during a system failure; HVAC risk assessment; and change control analysis including the impact of modifications requested by the end user. The course is designed to provide the attendee with thorough knowledge of the following topics: •The governing regulatory agencies with direct impact on HVAC systems •FDA and EU classified space comparison •What constitutes Good Engineering Practice •The major components of an HVAC system •A high level overview of Psychrometrics
  • 13 Request Info

    Advanced Tools and Techniques for Data Analysis

    This 2-day advanced analytics seminar will introduce you to predictive analytics techniques, so you can frame strategic and operational questions involving marketing, finance, and operations or other real-world business applications.

    In this hands-on course, you will cover a variety of analytics tools, such as histograms, ANOVA analysis, A/B testing, Pareto analysis, clustering, box plots, scatter diagrams, partitioning, unstructured text analysis, and multivariate regression analysis. Best of all, no background in statistics or programming is required. As long as you have a basic understanding of spreadsheets, you will learn how to manipulate complex data sets so you can gain insights that are not possible with common business intelligence techniques.

  • 14 Request Info

    Webinar: Service Level Agreements (SLAs) - Preparation Guidelines for Effective SLAs by Javier Kuong

    Who Will Benefit: Line senior executives responsible for company operations performance IT and quality assurance professionals Legal counsel officers that help develop agreements and service contracts Purchasing and Procurement Executives Legal Counsel Functions (Internal or External) Corporate and Internal Audit Executives, Internal and Information System Auditors Executives Dependent on Key Support Infrastructure Services, Such as IT and other business services Contingency Planning and Emergency Preparedness Professionals that must specify SLAs CIOs, CFOs, and any C-level Executive that Vitally Dependent on or that oversees Business Services External Auditors and Consultants in Risk Management and Contingency Planning Chief Risk Managers and Chief Security Officers (CSOs) and Professionals Individual Responsible for Negotiating Outsourced Services Compliance and Regulatory Mandate Officers/Professionals
  • 15 Request Info

    Breakthrough Six Sigma

    A simplified and powerful approach to Six Sigma that delivers breakthrough results fast. Apply the DMAIC process in services, operations and manufacturing. Fast cycle time, lean operations and other approaches covered as needed.
  • 16 Request Info

    Breakthrough Process Redesign

    Learn the five-step Breakthrough Process Redesign approach and apply it in the training session to your most crucial business, service or manufacturing process. Clients have saved millions, and the training pays for itself.
  • 17 Request Info

    Critical Thinking Challenge (Business Simulation)