Engineering Management

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  • 1 Request Info

    6-Hour Virtual Seminar on GxP/GMP and its Consequences for Quality Management

    GxP/GMP regulations are required to be used in regulated industries such as food, pharmaceutical, medical devices, and cosmetics. GMP regulations describe required quality management system for production and testing of products in these regulated industries. The purpose of the GMP regulations is to ensure that a product is safe and meets its intended use. Quality management system ensures that a product is safe and meets its intended use. Quality management system has four main components: quality planning, quality assurance, quality control, and quality improvement.
  • 2 Request Info

    A Risk Based Approach To IT Infrastructure Seminar 2018

    GxP Regulated companies are dependent on validated GxP computerized applications to conduct their day to day operations. These applications are, in turn, depended upon a qualified infrastructure that can be relied upon to provide control and regulatory compliance. The consequences of the IT Infrastructure being out of compliance can result in the failure of an entire site or geographic region being brought to a standstill while the compliance issue is resolved. It can also result in regulatory citations during a regulatory inspection as both the infrastructure be out of compliance and also cause the computerized applications that are dependent on it to be out of compliance.
  • 3 Request Info

    Collaboration 4 Project Results

    High energy, interactive 3-day PMBOK-based course for Proj.Mgrs. Teaches processes/ techniques for shaping, energizing, motivating project teams to get faster/better results with Collaboration,“The Tenth Knowledge Area.Bob Moir 404.338.0715
  • 4 Request Info

    Design Inputs Design Outputs Traceability Matrix

    Overview: If your design and manufacturing resources are spending too much time on documentation and not enough time on actual design and manufacturing you as a manager need to be looking for ways to simplify their work. Areas Covered in the Session: Brief introduction to Lean Documents and Lean Configuration. Quality System Regulation, 21 CFR Part 820, and ISO 13485 as these apply to design control documents. Traceability Matrix. Applying lean document and lean configuration principles to the above. Bringing it all together
  • 5 Request Info

    Design of Experiments Strategies | Six Sigma Process

    Join this webinar Design of experiments "DOE" which is a systematic method to determine the relationship between factors affecting a process and the output of that process. 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/Effective-Design-of-Experiments-DOE-Strategies-503955/JULY-2018-ES-TRAININGREGISTRY
  • 6 Request Info

    Effectively Manage Technical, IT, and Engineering Professionals

    Managing technical professionals requires special skills to apply general management principles. o Get results efficiently: plan, delegate, motivate, coach o Communicate; build engaged, high- performing team. o Experiential learning: customized case studies, self-assessments, Action Plan
  • 7 Request Info

    Fundamentals of Safety Engineering for Medical Devices

    Understanding the fundamentals of safety engineering for medical devices can make a tremendous difference in saving lives and help companies avoid costs of recall. 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/Safety-Engineering-Fundamentals-for-Medical-Devices-508813/JULY-2018-ES-TRAININGREGISTRY
  • 8 Request Info

    Investigating Sterility Test Failures

    Sterility testing is widely used in both the medical device and pharmaceutical industries. The pharmacopeia test is the official procedure for testing the sterility of pharmaceutical products. Despite its importance and its widespread use, many people are not aware of the limitations of the sterility test and are unsure how to proceed when a failure investigation occurs. 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/Investigating-Sterility-Test-Failures-503878/JANUARY-2018-ES-TRAININGREGISTRY
  • 9 Request Info

    It is not enough to Simply be a Project Manager

    Overview: We manage tasks and activities, and those activities must be performed by people, who must be led. It is not enough to simply be a Project Manager. Why should you Attend: On average it takes ten successful projects to make up for one really bad project. If your projects are finishing late, if your teams turn over faster than a freshman class in college, if your projects are losing money, then you need to take this course.
  • 10 Request Info

    Management/Leadership Power Tools for Engineers

    Engineers become managers because of technical expertise. They need a different skill set. Learn to communicate, plan, motivate, delegate, and coach effectively and efficiently using powerful, proven approaches tailored to your specific situation.
  • 11 Request Info

    MVP Training: Engineering Management

    MVP Seminars LLC, is a leading nationwide provider of business training seminars at affordable prices, with top-notch providers. Follow-up monitoring program no-charge! Please call 510-558-3495. Largest family run training business in USA.
  • 12 Request Info

    Webinar On 21 CFR Part 11 - Electronic Record and Signature Validation

    This Webinar will explain what 21 CFR Part 11 is, why it is important to FDA regulated companies and how conformance to Part 11 differs from just having good IT security. Procedures for controlling electronic signatures and electronic records will be explained.FDA regulated companies want to transition to electronic records for economy and efficiency.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-ELECTRONIC-RECORD-501906/DECEMBER-2016-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar on A Regulatory Perspective: FDA's New Guidance's Deciding When to Submit a 510(k) for Device & Software Changes

    Control of medical device changes and a current 510(k) are big issues in recent FDA studies. Companies are held fully responsible for deciding when a new 510(k) filing is warranted. Often this is a difficult decision process. Effective change control and the power of current risk management tools must be a major part of such an analysis. 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/A-Regulatory-Perspective-FDA-s-New-Guidance-s-Deciding-When-to-Submit-a-510-k-for-Device-Software-Changes-508234/MARCH-2018-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar on A well-designed On Boarding Program for GMP Environment

    This session will provide you with best practices for new employee orientation that can contribute to both GMP compliance and organizational productivity. 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/On-boarding-Employees-in-a-GMP-Environment-Best-Practices-For-Foundational-Employee-Success-507313/MARCH-2019-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar On Acceptance Activities in QSR

    Warning Letters from FDA frequently cite Acceptance Activities. In fact, it has been in the top five most frequently cited sections over the past few years. You can avoid a Warning Letter if you understand the regulations and develop processes to implement them. This presentation provides knowledge and tools to help implement an effective system that will withstand an FDA Inspection.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/ACCEPTANCE-ACTIVITIES-QSR-501690/OCTOBER-2016-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar on Acceptance Sampling Plans for Process Validation and Production Lot Monitoring

    Understand more about acceptance sampling plans for process validation and production lot acceptance by attending this audio conference. 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/Acceptance-Sampling-Plans-for-Process-Validation-and-Production-Lot-Monitoring-507734/JULY-2018-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar on ANDA Submission and GDUFA Guidance

    Understand how the submission process is structured and functions, in order to effectively and efficiently bring generic drugs and medicinal products to market. 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/ANDA-Submission-and-GDUFA-Guidance-504887/MARCH-2019-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar on Applying FMEA risk assessment to a sterility testing isolator

    This webinar discusses how the FMEA risk assessment tool should be applied based on a case study of a sterility testing isolator. 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/Applying-FMEA-risk-assessment-to-a-sterility-testing-isolator-508790/MARCH-2019-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar on Avoiding Investigational Failures and Reducing Discrepancies

    This webinar discusses avenues to be taken to avoid investigational failures and to reduce discrepancies. A robust investigational management system is always based on implementation of risk management and knowledge management pillars in pharmaceutical and biopharmaceutical organizations, as prescribed by ICH Q10. In addition, it is based on effective and efficient investigational practices which include formation of effective teams of subject matter experts and quality assurance representatives from these organizations.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/Avoiding-Investigational-Failures-and-Reducing-Discrepancies-509763/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar On Bad Standard Operating Procedures (SOPs) = Bad Training: Garbage In, Garbage Out

    Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical employees are required to perform. Still, it is not widely understood how the writing of a procedure can have a positive or negative impact on training. In this course you will learn the vital connection between the documentation and training spheres, and how to maximize this connection to improve the quality of both SOPs and training.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/BAD-STANDARD-OPERATING-PROCEDURES-SOPs-506264/AUGUST-2017-ES-TRAININGREGISTRY