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Courses

  • 41 Request Info

    Webinar on Supplier Quality Metrics and Scorecards A Systems Approach

    Join this 90-minutes webinar that focus on establishing an effective and efficient system of purchasing controls that enables to provide safe products to the customers. 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/Supplier-Quality-Metrics-and-Scorecards-A-Systems-Approach-502730/MAY-2018-ES-TRAININGREGISTRY
  • 42 Request Info

    Webinar on Best Practices for Implementing an Effective Cleaning Validation using Principles of Upcoming ASTM E3106

    Ninety minutes webinar on the Best Practices for Implementing an Effective Cleaning Validation. The speaker will also explain ASTM E3106 for Cleaning Validation. 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/Best-Practices-for-Implementing-an-Effective-Cleaning-Validation-using-Principles-of-Upcoming-ASTM-E3106-509617/MAY-2018-ES-TRAININGREGISTRY
  • 43 Request Info

    Webinar on Regulatory and Testing Requirements of the Bacterial Endotoxin Testing (BET) or LAL Program

    Importance of regulatory and testing requirements of products for compliance by applying sequential steps in testing product to rule out presence of Endotoxin. 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/Regulatory-and-Testing-Requirements-of-the-Bacterial-Endotoxin-Testing-BET-or-LAL-Program-507758/MAY-2018-ES-TRAININGREGISTRY
  • 44 Request Info

    Webinar on Scrutinizing Test Method Validation (TMV) to Verify the Performance of a Medical Device

    This webinar will help you have an understanding of successful Test Method Validation and the detailing of 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 https://www.onlinecompliancepanel.com/webinar/Scrutinizing-Test-Method-Validation-TMV-to-Verify-the-Performance-of-a-Medical-Device-504196/MAY-2018-ES-TRAININGREGISTRY
  • 45 Request Info

    Webinar on FDA's Medical Device De Novo Reclassification Process

    This webinar will examine and define De Novo and discuss the key elements of this classification 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/FDA-s-Medical-Device-De-Novo-Reclassification-Process-502304/MAY-2018-ES-TRAININGREGISTRY
  • 46 Request Info

    Webinar on The Paradigm of a High-Level System (HLS) in Quality

    This webinar will convey the understanding and rationale of High-Level System(HLS) approach with the revision of the ISO 9001:2015 standards. 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/The-Paradigm-of-a-High-Level-System-HLS-in-Quality-505696/MAY-2018-ES-TRAININGREGISTRY
  • 47 Request Info

    Webinar on GMP Complaint Systems, FDA's Adverse Event Reporting & Product Recalls

    Gain a clear understanding of what FDA inspectors look for when evaluating complaint handling and medical device reporting programs. 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/GMP-Complaint-Systems-FDA-s-Adverse-Event-Reporting-Product-Recalls-502220/APRIL-2018-ES-TRAININGREGISTRY
  • 48 Request Info

    Webinar on Managing Documents, Records, and Data for FDA Inspections

    This webinar can help you prepare a strategy for managing documents, records, and data during 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 https://www.onlinecompliancepanel.com/webinar/Managing-Documents-Records-and-Data-for-FDA-Inspections-505867/APRIL-2018-ES-TRAININGREGISTRY
  • 49 Request Info

    Webinar on Acceptance Activities in FDA's Quality Management System

    Understand how purchasing and acceptance activities are linked and combine to facilitate effective supplier 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/Acceptance-Activities-in-FDA-s-Quality-Management-System-507314/APRIL-2018-ES-TRAININGREGISTRY
  • 50 Request Info

    Webinar on Complying with FDA's Regulations for eCTD Submissions of all IND's NDA's

    How to ensure that you are ready for implementing the mandated requirements of the CTD & eCTD how to comply with the May 2018 electronic submission requirements Price:$350.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Complying-with-FDA-s-Regulations-for-eCTD-Submissions-of-all-IND-s-NDA-s-Are-you-Ready-for-the-May-5-2018-deadline-506512/APRIL-2018-ES-TRAININGREGISTRY
  • 51 Request Info

    Webinar on FDA - Streamlining Your Internal Auditing Process

    This webinar will cover creating of a value-added internal auditing program that is compliant to FDA cGMP/ Quality System Regulation and ISO 13485. It will include how to set up and manage the auditing system as well as how to conduct an internal audit and document the results and any nonconformities. It will discuss the value of a good internal auditing program. 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/FDA-Streamlining-Your-Internal-Auditing-Process-506001/MARCH-2018-ES-TRAININGREGISTRY
  • 52 Request Info

    Webinar on EU GMP Annex 1 - What's New for Sterile Product Manufacturing?

    A major revision is taking place with the European regulations covering the manufacture and distribution of sterile products. This is the first major update in 20 years, with the new draft text bringing in many changes, several of which will be far reaching. 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/EU-GMP-Annex-1-What-s-New-for-Sterile-Product-Manufacturing-507684/MARCH-2018-ES-TRAININGREGISTRY
  • 53 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
  • 54 Request Info

    Webinar on Medical Device Complaints & CAPA

    This webinar will explain the CAPA process from information gathering through MDR and Recall decision making to final CAPA closing. Post closing effectiveness evaluation is required and will be explained. Preventative Action is often neglected and will be discussed. Post distribution product monitoring including customer surveys will be explained. Integration of manufacturing non conformities with the CAPA program will be discussed. 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/Medical-Device-Complaints-CAPA-503680/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 55 Request Info

    Webinar on Fraud and Corruption Prevention in Contracts and Purchasing

    The old saying "An ounce of prevention is worth a pound of cure" is particularly applicable to procurement activities where fraud and corruption can raise not only the costs and risks of doing business but also jeopardizes the reputation of the organization and even the safety of employees and the general public. 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/Fraud-and-Corruption-Prevention-in-Contracts-and-Purchasing-503405/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 56 Request Info

    Webinar on Time Series Analysis Using MS Excel

    Medical device manufacturers must analyze complaints, process data, non-conformances, service records, internal quality audits, etc. This analysis, using appropriate statistical methodology under §820.100 and ISO 13485:2016, 8.4, identifies issues in the quality management system. The result can lead to corrective action and other improvement opportunities. 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/Time-Series-Analysis-Using-MS-Excel-502148/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 57 Request Info

    Webinar on Implementation of a Successful Technology Transfer Process

    This training will introduce the concepts associated with implementing a carefully defined technical and business governance program along with clearly defined R&D to site transfer steps for successful implementation. It will cover the concepts associated with transferring the scientific technology needed to manufacture the product, processes to ensure the receiving manufacturing facility is ready for the product and tools and templates to help capture the knowledge. 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/Implementation-of-a-Successful-Technology-Transfer-Process-509919/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 58 Request Info

    Webinar on Objectionable Microorganisms - Knowing What and Where You Can Find Them in Biopharmaceutical Manufacturing

    Objectionable microorganisms are considered, if discovered, harmful to the patient. By identifying and controlling these microorganisms and putting the appropriate controls in place early in the pharmaceutical manufacturing or medical device manufacturing processes problems in the patient can be prevented. This webinar will review the regulations pertaining to objectionable microorganisms, agency expectations, methods to identify objectionable microorganisms, interpreting results, and controls to put into place. By knowing, where, when, why, and how objectionable microorganisms exist, harmful consequences to the patient can be prevented. 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/Objectionable-Microorganisms-Knowing-What-and-Where-You-Can-Find-Them-in-Biopharmaceutical-Manufacturing-508673/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 59 Request Info

    Webinar on Understanding Combination Products: Navigating the Rules and Regulations

    This training will help you understand what a combination product is, highlight some of the changes in how the FDA views combination products, the approval steps for combination products and proposed regulations for these types of products.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/Understanding-Combination-Products-Navigating-the-Rules-and-Regulations-508549/FEBRUARY-2018-ES-TRAININGREGISTRY
  • 60 Request Info

    Webinar on General Mexican labeling specifications for pre-packaged foods and non-alcoholic beverages-commercial and sanitary information (NOM-051-SCF

    General Mexican labeling specifications for pre-packaged foods and non-alcoholic beverages has been submitted to different changes due to health policies in Mexico. In order to comply with the new guidelines you’ll need to include in your label the new front of package icons. How you need to calculate, place and declare the information for them are requirements subject of NOM-051-SCFI/SSA1-2010. 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/General-Mexican-labeling-specifications-for-pre-packaged-foods-and-non-alcoholic-beverages-commercial-and-sanitary-information-NOM-051-SCFI-SSA1-2010-504263/JANUARY-2018-ES-TRAININGREGISTRY