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Courses

  • 1 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
  • 2 Request Info

    Webinar on Software Validation & Testing - Regulatory Requirements

    This webinar give an understanding of software designing device for reliable and safe performance is critical for efficient business strategy. 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/Software-Validation-Testing-Regulatory-Requirements-505462/JUNE-2018-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar on How to Improve Export Compliance with Effective Audits

    Learn how you can utilize export audits to assess the effectiveness of current export compliance processes and check for inconsistencies between these and day-to-day operations. Armed with the data following the audit, you can assess the next steps to validate the existing program or correct deficiencies. 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/How-to-Improve-Export-Compliance-with-Effective-Audits-504409/MARCH-2018-ES-TRAININGREGISTRY
  • 4 Request Info

    Webinar on Increasing Market Share by Increasing Share of Mind

    Understanding the brain's four thinking preferences - and how these preferences translate into consumer Buying Styles, will enable you to create not only a better brand - but also an innovative branding and marketing strategy. The bottom line: BrainBranding connects your brand with more people. 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/Increasing-Market-Share-by-Increasing-Share-of-Mind-507491/MARCH-2018-ES-TRAININGREGISTRY
  • 5 Request Info

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

    FDA regulates firms' use of social media to prohibit product information that is deemed false and misleading. Firms bear the responsibility of checking and prohibiting the use of social media that offends FDA's key limitations of how social media can be used. What can be stated by an individual citizen becomes restrict commercial speech when such statements or related information is attributed to a manufacturer. FDA's treatment of social media as labeling opens up a broad opportunity for FDA to claim your product is illegal. Staying within the vague boundaries of FDA's social media restrictions can be confusing, surprising and expensive if you have not carefully charted your course on the use of social media. 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-Off-label-Promotion-in-Social-Media-509203/JANUARY-2018-ES-TRAININGREGISTRY
  • 6 Request Info

    Kano Analysis for Product Decisions

    Kano Analysis, an important tool for product development, uses a structured methodology to help determine important device characteristics. For example, if customers expect a device will have a certain feature, they would be disappointed if it isn't there. However, if it were there, it doesn't create satisfaction; it was assumed.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/Kano-Analysis-for-Product-Decisions-508099/JANUARY-2018-ES-TRAININGREGISTRY
  • 7 Request Info

    Webinar On Mobile Medical Apps (Is It a FDA Regulated Device?) and Cybersecurity

    With mobile platforms more user friendly, and with computers, tablets and smart phones becoming more powerful, we see an increase in the offering of apps. Some of these apps are specifically targeted to assist individuals in the management of their health and wellness, while other apps are targeted to healthcare providers as tools to assist in the delivery of care.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/MOBILE-MEDICAL-APPS-CYBERSECURITY-509085/AUGUST-2017-ES-TRAININGREGISTRY
  • 8 Request Info

    Webinar On Understanding HTSUS and Schedule B Code Classifications

    Importers and exporters alike require a firm understanding of the Harmonized Tariff Schedule of the United States (HTSUS) and the Schedule B Code in order to properly apply the rules for classifying their products for import and export. Tariff classifications drive the duty rates that will be applied to imported merchandise, while Schedule B Codes (as well as their HTSUS classification counterparts) are required to be reported in exporters' Electronic Export Information (EEI) filings submitted into the Automated Commercial Environment.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/HTSUS-SCHEDULE-B-CODE-CLASSIFICATIONS-508656/AUGUST-2017-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar On Applying Human Factors and Usability Engineering Throughout the Medical Device Development Lifecycle

    For medical device manufacturers, human factors engineering has gradually become part of the standard expectations for products on an FDA approval pathway. Though it is possible to execute successful studies that only meet the FDA's minimum standards for human factors, this strategy does not necessarily result in products that have been optimized for safety and usability.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-DEVELOPMENT-LIFECYCLE-505949/JULY-2017-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar On USA and Canada Food Marketing Claims

    This webinar on Food Manufacturing Claims will detail the labeling requirements for foods under the Federal Food, Drug & Cosmetic Act and its amendments in addition to the CFIA and Health Canada.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/USA-CANADA-FOOD-MARKETING-CLAIMS-503642/JUNE-2017-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar On How to Prepare for a Customs Focused Assessment Audit and Self Audit your Import Program

    This webinar deals with a very serious Import Compliance topic, Customs Focused Assessment Audits. The attendee will be educated on what a Focused Assessment is, how they are assigned, costs involved and how to avoid one. It will protect you from business disruption, fines and penalties that can result from regulatory intervention from U.S. Customs and Border Protection.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-FOCUSED-ASSESSMENT-509955/MAY-2017-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar On Requirements for Registration of Medical Device Products in China

    China's medical device market is rapidly growing these years, China offers numerous opportunities for foreign healthcare related companies but understanding the practicalities of accessing the market is not simple. Attend this training, if you are a manufacturer or distributor involved in exporting medical devices or IVDs to China, this webinar will provide you with necessary briefing on CFDA registration of 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/MEDICAL-DEVICE-PRODUCTS-CHINA-502010/JANUARY-2017-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar On Complying with Mexico Food Labeling Requirements: Retail & Private Label Opportunities in Mexico

    All importers and producers of processed food products must be aware of the new regulations and apply it in their labels for final consumer. Attend the webinar to know and understand the Mexican labeling standard as well as and the new requirements regarding the use of Front of Pack icons and the voluntary request of a nutritional Logo. The speaker will also explain the steps to follow in order to gain an 'organic' status.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/MEXICO-FOOD-LABELING-502016/JANUARY-2017-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar On Mexican Import Process

    Since the implementation of NAFTA, Mexico has become a major market for USA exporters. This course will provide an in-depth explanation of the Mexican importing process, including specific rules and documentation. The webinar will also discuss what impact local government and private resources will have on the exporter's transaction process when it comes to tariff costs in this trading environment.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/MEXICAN-IMPORT-PROCESS-501985/DECEMBER-2016-ES-TRAININGREGISTRY
  • 15 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
  • 16 Request Info

    Webinar On Lending Compliance for Adjustable Rate Mortgages

    This webinar will help you to understand how interest rates and adjustable rate mortgages work, learn all the components of an adjustable rate mortgage, understand how interest rates work in general, understand the different indexes on which ARMs are based and understand different residential loan programs that are available.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/LENDING-COMPLIANCE-ADJUSTABLE-MORTGAGE-501971/DECEMBER-2016-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar On CMC Considerations for Successful Regulatory Submission

    This webinar is intended to provide advice on the level of detail required for regulatory submissions at different program phases. Regulatory strategy across the development program will also 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://onlinecompliancepanel.com/webinar/CMC-REGULATORY-SUBMISSION-501931/DECEMBER-2016-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar On The Global Business Model for International Trade

    This 60-minute webinar will help exporters and importers understand the accepted business practices for doing business internationally to include the Sale, the Performance, the Logistics and the Settlement phases of global business.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/GLOBAL-BUSINESS-INTERNATIONAL-TRADE-501852/DECEMBER-2016-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar On FDA Action on Antiseptic Wash Products: What is Next for the Industry?

    The FDA just banned 19 active ingredients that are used in antibacterial soaps. This major regulation will have a huge impact on this multi-million-dollar industry since the FDA Rule will require companies to remove these ingredients from their products or remove the products from the market. Manufacturers will have one year to take these products off the market or reformulate them.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/FDA-ACTION-ASPECTIC-WASH-PRODUCTS-501903/DECEMBER-2016-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar On Device Master Record - Can DMR show the way to comply with QSR?

    Device Master Record (DMR) is the output of design controls and the source document for every medical device. An accurate, complete DMR gives the 'recipe' for making a medical device. From the smallest component or ingredient and simplest operation or step to the finished medical device including labels, labeling, primary, secondary and beyond packaging to installation, servicing and maintenance instructions, the DMR has everything including the exact format and content of a medical device's device history record (DHR/batch record).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/DEVICE-MASTER-RECORD-501904/DECEMBER-2016-ES-TRAININGREGISTRY