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Courses

  • 1 Request Info

    Good Documentation Guideline (Chapter 1029 USP)

    Overview: Good Documentation Practices (GDP) is a critical and essential part of a regulated environment (pharmaceutical and medical device manufacturing, R&D, laboratories and clinical trials). Compliance with GDP ensures an auditable account of work. It ensures integrity and control of documents and is a key requirement for a developed quality system. This training session will cover the US Pharmacopeia General Chapter <1029> and all aspects of GDP including practices for writing and correcting documentation.
  • 2 Request Info

    Webinar on Guidance on Elemental Impurities - According to ICH Q3D & USP 232/233

    Learn about elemental impurities either through thorough risk assessments or through testing. And it will provide an understanding of the standards and guidelines. 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/Elemental-Impurities-Tests-for-Pharmaceutical-Products-according-to-the-ICH-Q3D-and-USP-232-233-Guidelines-507031/APRIL-2019-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar on The Importance of the Bacterial Endotoxin Testing (BET) or LAL Program

    Attend this course to understand how the Bacterial Endotoxin Testing (BET) or LAL Program works and how this testing program can be applied to quality control. 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/Regulatory-and-Testing-Requirements-of-the-Bacterial-Endotoxin-Testing-BET-or-LAL-Program-502915/APRIL-2019-ES-TRAININGREGISTRY
  • 4 Request Info

    Webinar on Human Error Reduction in GMP Related Environments

    You will learn practical methods to reduce human performance issues in GMP related environments. 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/Human-Error-Reduction-in-GMP-Related-Environments-509147/MARCH-2019-ES-TRAININGREGISTRY
  • 5 Request Info

    Webinar on FDA's Off-label Promotion in Social Media

    Learn how to stay compliant from FDA's regulations on use of social media about how to manage marketing strategies. 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-s-Off-label-promotion-in-Social-Media-505627/MARCH-2019-ES-TRAININGREGISTRY
  • 6 Request Info

    Webinar on Stability Studies and Estimating Shelf Life with Regression Models

    Learn various useful techniques for studying stability and determining the shelf life of a product with the resulting data. 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/Stability-Studies-and-Estimating-Shelf-Life-with-Regression-Models-509644/MARCH-2019-ES-TRAININGREGISTRY
  • 7 Request Info

    Webinar on Analytical Method Validation and Transfer

    This course provides guidance on tools to plan and execute test method validation and transfer also a comprehensive overview of the international regulatory authority requirements. 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/Analytical-Method-Validation-and-Transfer-506228/MARCH-2019-ES-TRAININGREGISTRY
  • 8 Request Info

    Webinar on Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory

    What are the strategies to be implemented before your laboratory undergoes a GMP inspection. Join the webinar to learn more. 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/Laboratory-Inspection-Readiness-Implementing-GMPs-for-the-Pharmaceutical-Laboratory-504036/JANUARY-2019-ES-TRAININGREGISTRY
  • 9 Request Info

    FDA's 21 CFR 11 Add-On Inspections - Recent Updates

    Overview: In December 2010 FDA started the Part 11 inspection initiative. While originally the initiative was supposed to last 3-6 months, it has now turned into an ongoing program with Part 11 related issues being part of most future inspections. At the beginning of the initiative FDA made it very clear that Part 11 is in effect and is enforced according to the original Part 11 and the Guidance from 2003. In the meantime FDA officials reported about key findings. For example, George Smith who heads up FDA's Part 11 working group gave an update with examples of violations.
  • 10 Request Info

    Webinar on ISO 14644 - The Revised Standard and Implications for Cleanrooms

    The international standard for cleanrooms has undergone a major revision. This webinar discusses the revisions in the context of global GMPs and the overall contamination control strategy. The webinar discusses testing approaches and the assessment of test data. The learning point is with keeping cleanrooms compliant.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/ISO-14644-The-Revised-Standard-and-Implications-for-Cleanrooms-509318/AUGUST-2018-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar on Stunning Changes in FDA's Software Regulation

    Gain an understanding of how FDA is planning to give additional regulatory relief to its regulation of software, which has a startling change for premarket access. 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/Stunning-Changes-in-FDA-s-Software-Regulation-503201/JULY-2018-ES-TRAININGREGISTRY
  • 12 Request Info

    Guidance on Inactive Ingredients- FDA Update

    Attend this webinar to gain an appreciation of the regulatory CMC and use of inactive ingredients manufactured from various firms. 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/Discussion-Regarding-the-Substitution-of-a-New-Inactive-Ingredient-in-an-Approved-Parenteral-Drug-Product-505414/JULY-2018-ES-TRAININGREGISTRY
  • 13 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
  • 14 Request Info

    Webinar on Processing of cGMP Controlled Raw Materials

    Join this session to discuss the implementation of risk management and knowledge management pillars for the controlled substances systems at the pharmaceutical facilities. 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/Processing-of-cGMP-Controlled-Raw-Materials-504506/JUNE-2018-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar on Good Documentation Practices and Recordkeeping Regulations (FDA & EMA)

    Discuss the importance of good documentation practices/GDP and how to create lab notebook policies that meet regulators expectations. 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/Good-Documentation-Practices-and-Recordkeeping-Regulations-FDA-EMA-508525/MAY-2018-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar on Sunshine Act Reporting – Clarification for Clinical Research

    This webinar will examine the implications of the Sunshine Act for healthcare providers and life science companies. 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/Sunshine-Act-Reporting-Clarification-for-Clinical-Research-508714/MAY-2018-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar on Process Capability: When It's Not a Bell Curve

    This process capability webinar will show how to handle situations in which the distribution is not a bell curve. 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/Process-Capability-When-It-s-Not-a-Bell-Curve-505754/APRIL-2018-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar on Stability Studies and Estimating Shelf Life with Regression Models

    Manufacturers of foods, drugs, consumer goods, and other products must determine the shelf life of their products so that customers know when the product can be expected to perform as intended. Many approaches are available to quantify the "shelf life" and the method(s) chosen often depend on the testing time available. 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/Stability-Studies-and-Estimating-Shelf-Life-with-Regression-Models-506813/MARCH-2018-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar on Mastering Excel Pivot Tables: The Ace Analytical Tool of Excel

    A very common situation in Excel is the Big List. You might have a huge list of employees, customers, products, sales, events, locations, technical support tickets - it doesn't really matter what the list is of, what matters is that there is value in that list. You might want to know what your most profitable kind of customer is, or which technical support rep is being most productive, or which product is driving the most interest, but the Big List isn't giving you that information automatically. Building a Pivot Table is a fast, easy way of analyzing your data and giving you useful insights. If you want to know how to help your business, creating a summary and a chart with Pivot Tables should be your first move. 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/Mastering-Excel-Pivot-Tables-The-Ace-Analytical-Tool-of-Excel-506657/FEBRUARY-2018-ES-TRAIN
  • 20 Request Info

    Webinar on Precisely Wrong: The Materials Planning Challenge in a Dynamic 21st Century

    What if there was one fatal flaw in MRP that makes it completely incapable of conveying relevant information? What if correcting this one fatal flaw allowed the promise of MRP to be attained? Join this webinar with expert speaker Carol Ptak, who will describe what the real issue is and just how devastating the problem can be for supply chain management. 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/Precisely-Wrong-The-Materials-Planning-Challenge-in-a-Dynamic-21st-Century-502299/JANUARY-2018-ES-TRAININGREGISTRY