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  • 1 Request Info

    Webinar On Secrets for Writing Excellent SOPs (Standard Operating Procedures)

    Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well written SOPs ensure that your personnel can consistently and accurately follow your processes resulting in correct outcomes and quality work. This webinar will help you structure your QMS and develop accurate, clear, unambiguous SOPs.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/SECRETS-WRITING-EXCELLENT-SOPs-504929/MARCH-2017-ES-TRAININGREGISTRY
  • 2 Request Info

    Webinar On Three Years into the Drug Supply Chain Security Act (DSCSA): Where Does Industry Stand?

    The federal Drug Supply Chain Security Act (DSCSA) established new licensing, track-and-trace and preemption requirements for prescription pharmaceutical manufacturers, distributors and dispensers in the U.S. Three years have now passed since enactment of this law, but FDA has yet to publish key implementation standards. In the meantime, industry must comply with various deadlines. Individual state agencies also continue to act to fill perceived voids, complicating efforts toward national uniformity for operations.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/DRUG-SUPPLY-CHAIN-SECURITY-ACT-DSCSA-502056/MARCH-2017-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar On How will Artificial Intelligence (AI) Affect Healthcare?

    I is moving into Healthcare rapidly. There are many models that AI will engage. This topic will cover the new field of AI, its capabilities and how it will impact all aspects of the Healthcare from Supply Chain, to Population Health to direct consumer/patient engagement.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/ARTIFICAL-INTELLIGENCE-AFFECT-HEALTHCARE-505512/MARCH-2017-ES-TRAININGREGISTRY
  • 4 Request Info

    Webinar On Understanding and Overcoming Challenges Encountered in Implementing the New ISO 13485:2016 Standard for Medical Device Quality Systems

    You will gain a thorough insight into the specific quality system requirements of the all new International ISO 13485:2016 Quality System Standard requirements for Medical Devices.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/NEW-ISO-13485-MEDICAL-DEVICE-QUALITY-SYSTEM-507815/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 5 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
  • 6 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
  • 7 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
  • 8 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
  • 9 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
  • 10 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
  • 11 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
  • 12 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
  • 13 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
  • 14 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
  • 15 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
  • 16 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
  • 17 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
  • 18 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
  • 19 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
  • 20 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