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  • 1 Request Info

    Workshop On Quality Audits for the Medical Device Industry

    Quality audits are an important element in implementing and maintaining an effective Quality Management System (QMS). Audits are one of the most powerful tools that management has to assure on effective QMS.Price:$1400.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link
  • 2 Request Info

    Webinar On Microsoft Excel Series - Part 2: Learn More about Macros

    Part 2 of the Microsoft Excel macros series presented by Excel expert David Ringstrom, CPA, will define how to adjust Excel's macro security settings. Attendees will learn how to apply an enhanced understanding of Visual Basic for Applications (VBA) macros and how to enhance the code you have created with the Record Macro feature.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/MICROSOFT-EXCEL-SERIES-PART-2-502004/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar On Quality by Design

    This webinar will help you learn the basics of design controls for medical devices. This webinar will focus on the fundamental concept that quality cannot be inspected in--it must be designed in. We'll cover the regulations and expectations for design control. We'll discuss how design control fits into your Quality Management System. Successful integration can enhance your new product development process.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-DESIGN-502012/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 4 Request Info

    Webinar On Disaster Recovery (DR) and Business Continuity Planning (BCP) Best Practices for an FDA-Regulated Environment Increasingly Challenged by Cy

    This course is intended to provide specific guidelines for coaching attendees on the best practices for Disaster Recovery (DR) of computer systems and data and for Business Continuity Planning (BCP), including the handling of documentation in the event operations are disrupted. We will discuss the various types of risks, including cyber threats, power outages and others that could render an organization paralyzed in the absence of good planning.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/DR-BCP-FDA-CYBER-ATTACKS-502020/JANUARY-2017-ES-TRAININGREGISTRY
  • 5 Request Info

    Webinar On The Blue Print for Implementing Pharmaceutical and Medical Device Quality Management System under one Umbrella

    As the global distributers and manufacturers of Medical devices and pharmaceuticals expand their quality management system (QMS) to cover the pharmaceutical and medical device requirements under one umbrella, the need to understand the quality system requirements that are unique to each industry becomes very crucial.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/BLUE-PRINT-PHARMACEUTICAL-MEDICAL-DEVICE-501995/JANUARY-2017-ES-TRAININGREGISTRY
  • 6 Request Info

    Webinar On Implementation of the generic drug labeling rules 2017

    FDA is due to release a major Generic Drug Labeling Rule in April 2017. Attend this training to review current generic drug labeling rules and requirements and how they will change with the new rule. Understand the obligations and responsibilities for complying with the new rule as well as how to make submissions to change the product labeling.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/GENERIC-DRUG-LABELLING-RULES-2017-501970/DECEMBER-2016-ES-TRAININGREGISTRY
  • 7 Request Info

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

    This webinar will cover acceptance sampling plans for process validation and production lot acceptance. Sampling plans for attribute data are the primary focus although variable acceptance sampling plans are presented as well. The binomial distribution and its use in developing Operating Characteristic (OC) curves 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 http://www.onlinecompliancepanel.com/webinar/PROCESS-VALIDATION-PRODUCTION-LOT-MONITORING-501949/JANUARY-2017-ES-TRAININGREGISTRY
  • 8 Request Info

    Webinar On Employer Beware: is your Non-compete Enforceable?

    Employers routinely require employees to enter into noncompete and nonsolicitation agreements upon commencing employment in order to protect confidential information, trade secrets and business relationships from being used for competitive advantage. Once an employee executes noncompetition and nonsolicitation covenants (often referred to as restrictive covenants), many employers assume such information and relationships will be legally protected after the employee separates from employment. This is not necessarily the case.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/EMPLOYER-BEWARE-501974/DECEMBER-2016-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar On Effective Corrective and Preventive Action Program (CAPA): The Role of Corrective Action and Preventative Action in Your Quality Management

    Corrective and Preventive Actions (CAPAs) are a beneficial tool for documenting potential problems and investigating them through root cause analysis. Today, more companies are utilizing CAPAs to properly document investigations and capture the action taken by the company. This session will cover the CAPA process, how to implement an effective CAPA system using a risk-based approach and review the key elements of a CAPA report.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/CORRECTIVE-PREVENTIVE-ACTION-PROGRAM-CAPA-501961/DECEMBER-2016-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar On Pharma Analytics - I Have All These Data, Now What Do I Do?

    We know that it takes more than a large data set and computer software to effectively solve problems. As information technology increases in capability and availability, the opportunity to use data to develop and improve processes becomes even greater. Particular attention is paid to the pedigree of the data: the process that generated the data, the measurement process and the data collection process including the sampling schemes used.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/PHARMA-ANALYTICS-501913/DECEMBER-2016-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar On Safe Work Practices: OSHA Compliance with Flammable and Combustible liquids

    Flammable materials are substances that can ignite easily and burn rapidly. They can be common materials that are at the most work sites in gas, liquids or solids. In addition, flammable materials may themselves represent a health hazard. This webinar will cover only the flammable and combustible liquids handling and storage. This webinar will cover OSHA and NFPA standards that govern the handling and storage of these liquids. 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/SAFE-WORK-PRACTICES-501670/DECEMBER-2016-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar On Using US Customs FREE ACE Portal to Improve Import Compliance & Identify Strategic Opportunities

    Join this session by expert speaker Randi S. Waltuck Barnett to see a practical demonstration of establishing a FREE US Customs ACE portal account, extracting meaningful reports on a timely basis, and best practices for analyzing extracted data. Also, find hidden data sources to help you ensure that you have complete and accurate data at your disposal, to prove that you are exercising reasonable care, and mitigating your import compliance risks.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/US-CUSTOMS-FREE-ACE-PORTAL-IMPORT-COMPLIANCE-501876/DECEMBER-2016-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar On 21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration

    All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form of records. Medical device manufacturing plants, required to follow 21 CFR Part 820, have the additional responsibility to ensure that each and every step of the manufacturing process is controlled by work instructions, SOPs, set-up instructions, equipment maintenance, and support functions, and that evidence of this work is maintained by controlled records.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-PART-820-QUALITY-SYSTEM-501907/DECEMBER-2016-ES-TRAININGREGISTRY
  • 14 Request Info

    Two Days Workshop On Quality Audits for the Medical Device Industry

    Quality audits are an important element in implementing and maintaining an effective Quality Management System (QMS). Audits are one of the most powerful tools that management has to assure on effective QMS.Price:$1400.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/workshop/Quality-Audits-for-the-Medical-Device-Industry-800014/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar On The New IRS Partnership Audit Rules: Why Every Partnership and LLC Operating Agreement will Require Amendment

    This webinar will examine the new IRS partnership audit rules that were enacted in November 2015. Virtually every Partnership Agreement and Operating Agreement will in all likelihood need to be amended to take into account at least portions of these new rules. Under these rules, the IRS will audit the partnership as a separate taxable entity, and if there is an assessment, make the assessment against the partnership itself, not the individual partners.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/NEW-IRS-PATNERSHIP-AUDIT-RULES-501879/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar On Introduction to Country of Origin

    In this session, we'll review the basics of Origin, Globally, Regionally, and Nationally. Included will be the various agencies that oversee Origin matters and the concepts of non-preferential and preferential origin, such as the WTO, WCO, FCA, US CBP, and others. Further, we'll take a high-level look at the determination of origin, its applications, and the challenges and complexity of 'origin'.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/INTRODUCTION-COUNTRY-ORIGIN-501743/NOVEMBER-2016-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar On Preparing for and Defending Against a Customs Audit

    This webinar will review the legal framework surrounding your imports under Customs Law and Regulation. We'll discuss the concept of 'reasonable care' and describe some of the best practices for your on-going internal control program in this business critical area, including COSO standards, do's and don'ts, lessons learned, and best practices to help you successfully prepare for and defend yourself against a Government Customs Audit.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/DEFENDING-AGAINST-CUSTOMS-AUDIT-501746/OCTOBER-2016-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar On What to Do When the DOT Hazardous Materials Enforcement Inspector Comes Knocking

    $175,000 Per Day is the Cost of a Hazardous Material Shipping Violation-Know How to Avoid These Costly Mistakes in 60 minutes! Join this webinar to get insights into what to expect from a hazardous materials inspection and how to make the best of it. Be better prepared to minimize exposure to violations and avoid penalties that can exceed $175,000 per infraction per day.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/DOT-HAZARDOUS-ENFORCEMENT-501729/OCTOBER-2016-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar On Understanding Vendor Verification and Monitoring Programs for Food Manufacturing

    Vendor verification has become a very important part of ensuring safe and quality ingredients for food manufacturing. All of the internal programs that are put in place within a manufacturer may not overcome issues that arrive from your vendors at your receiving docks.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/VENDOR-VERIFICATION-PROGRAMS-FOOD-MANUFACTURING-501681/SEPTEMBER-2016-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar On What is the Correct ERP software for my organization?

    Enterprise Resource Planning (ERP) software is designed to enhance your business, but not every business is the same. To ensure that you select the right ERP software to obtain the maximum benefits and return on investment for your manufacturing or distribution business, a thorough ERP evaluation process is the key.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/ERP-SOFTWARE-MY-ORGANIZATION-501678/SEPTEMBER-2016-ES-TRAININGREGISTRY