Manufacturing Fundamentals

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Courses

  • 1 Request Info

    Webinar on The Hatto ("Sudden Awareness") Report - Use Stakeholder-Initiated CAPA to Drive Improvement

    This webinar will present use of Hatto (sudden awareness) report, stakeholder-initiated CAPA to drive improvement. Price:$150.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link - https://www.onlinecompliancepanel.com/webinar/The-Hatto-Sudden-Awareness-Report-Use-Stakeholder-Initiated-CAPA-to-Drive-Improvement-507502/FEBRUARY-2019-ES-TRAININGREGISTRY
  • 2 Request Info

    Webinar on Implementing the ASTM E2500 Validation Method

    This validation training program will discuss regulatory requirements from the FDA, EU and ICH perspective, review all the detailed guidance on the concepts found in ASTM E2500 to help industry professionals understand how to implement a validation program based on the ASTM 2500 Approach. Price:$150.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link - https://www.onlinecompliancepanel.com/webinar/Implementing-the-ASTM-E2500-Validation-Method-509460/FEBRUARY-2019-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar on Efficient and Effective Batch Record Reviews to Improve your Process Capabilities

    Understand regulatory requirements for batch record review and what to look for while reviewing batch records. Register for this webinar today. Price:$150.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link - https://www.onlinecompliancepanel.com/webinar/Efficient-and-Effective-Batch-Record-Reviews-to-Improve-your-Process-Capabilities-506336/JANUARY-2019-ES-TRAININGREGISTRY
  • 4 Request Info

    Pharmaceutical Drug Registration in China

    Overview: Bringing pharmaceutical products to market in China has become much easier for foreign companies. The Chinese FDA (CFDA), now renamed as CNDA, recently made a series of significant changes to the marketing authorisation regulations by issuing a large number of guidelines and opinions (in Chinese).
  • 5 Request Info

    Webinar on FDA Regulations for Analytical Instrument Qualification and Validation Processes

    In this webinar you will learn the different global agencies expectations of analytical equipment qualification along with the development of a sound process validation program in order to develop and implement bulletproof solutions that are accepted, effective, and efficient. Through case study analysis we will examine best practices to provide thoughts and ideas to develop or improve the performance of your current system. 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/FDA-Regulations-for-Analytical-Instrument-Qualification-and-Validation-Processes-504473/JANUARY-2018-ES-TRAININGREGISTRY
  • 6 Request Info

    Preventive Maintenance Essential Care & Inspection Techniques Training Course

    IDCON's practical training course for maintenance technicians and operators teaches how to care for equipment and perform fundamental condition monitoring (inspection) techniques. Participants learn the basics behind effective lubrication, balancing, alignment, cleaning, electrical and installation practices. They will learn about common components such as motors, bearings, gearboxes and much more.
  • 7 Request Info

    The Regulated Medical Marijuana Business - An Educational Seminar from Concept to Product Sale

    Upon completion of this course, each participant will have an in-depth overview and understanding of the medical marijuana industry starting with the business concept and ending with product sale. Tools, methods and techniques will be employed throughout the course topics to help ensure the planning and execution process is completed in a timely manner while avoiding the typical pit falls that increase cost and extend schedules. Generally acceptable good manufacturing practices and good engineering practices will be integrated throughout the course to provide a robust and repeatable process for compliance with maximum uptime to enable a return on investment. Employee training, building system commissioning and validation, security, cleaning, sanitization and other Standard Operating Procedures (SOPs) will be introduced.
  • 8 Request Info

    Webinar On CE Mark - Required to Sell in the European Market

    Medical devices sold into the European Union (EU) must comply with the applicable medical device directives, EU laws similar to FDA's regulations. Medical devices declared compliant must bear a CE mark in order to be admitted into the 29 member countries comprising the EU.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/CE-MARK-REQUIRED-SELL-EUROPEAN-MARKET-501636/AUGUST-2016-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar on Normality Tests and Normality Transformations: Explanations

    Overview: Normality Tests and normality transformations are a combination of graphical and numerical methods that have been in use for many decades. These methods are essential to apply whenever a statistical test or method is used whose fundamental assumption is that the inputted data is normally distributed. Normality "testing" involves creating a "normal probability plot" and calculating simple statistics for comparison to critical values in published tables. Contact Detail: NetZealous - Compliance4All, 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA. Phone: +1-800-447-9407 Email: support@compliance4All.com http://www.compliance4all.com/ Event Link : http://bit.ly/Normality-Tests-and-Transformations
  • 10 Request Info

    Applied Statistics for QA, QC, Manufacturing, and Design Control

    This seminar provides a practical approach to understanding how to interpret and use a standard tool-box of statistical methods, including confidence intervals, t-tests, Normal K-tables, Normality tests, confidence/reliability calculations, AQL sampling plans, measurement equipment analysis, and Statistical Process Control. Without a clear understanding and correct implementation of such methods, a company risks significantly increasing its complaint rates, scrap rates, and time-to-market; and significantly reducing its product and service quality, its customer satisfaction levels, and its profit margins.