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  • 1 Request Info

    Webinar on Combination Products - Identify and Navigate Regulations

    Attend this training to understand the definition of combination products and determine the required regulations from FDA. Price:$229.00. 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-503612/SEPTEMBER-2019-ES-TRAININGREGISTRY
  • 2 Request Info

    Webinar on Classifying Medical Devices, The De Novo Process and the FDA's Final Rule to Simplify Medical Device Classification Procedures

    This webinar will review the Medical Device Classification Procedures which includes the De Novo process in conjunction with the recent changes to 21 CFR 860 that pertain to the reclassification of the post amendment devices and the De Novo process in general. 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/Classifying-Medical-Devices-The-De-Novo-Process-and-the-FDA-s-Final-Rule-to-Simplify-Medical-Device-Classification-Procedures-506011/FEBRUARY-2019-ES-TRAININGREGISTRY
  • 3 Request Info

    Webinar on Discussion on Raw Material Methods and Specifications (Active and Inactive Ingredients) Referenced in UPS, EP, and JP Compendia

    The webinar on Raw Material Methods discusses how FDA has approved hundreds of inactive ingredients for thousands of products with various dosage forms. 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/Discussion-on-Raw-Material-Methods-and-Specifications-Active-and-Inactive-Ingredients-Referenced-in-UPS-EP-and-JP-Compendia-509975/MAY-2018-ES-TRAININGREGISTRY
  • 4 Request Info

    Webinar on Understanding the Regulation of Prescription Drugs

    Get trained on FDA regulation of Rx drug products and learn tools needed to develop and produce an OTC drug product for marketing and sale in the U.S. 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-the-Regulation-of-Prescription-Drugs-505262/MAY-2018-ES-TRAININGREGISTRY
  • 5 Request Info

    Webinar on Global Harmonization with New SDS (Safety Data Sheet) Format

    OSHA has made a significant revision to the HazCom Standard with the new Globally Harmonized Standard (GHS) with a new Safety Data Sheet (SDS) format. This webinar will give participants a comprehensive overview of the new OSHA GHS 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/Global-Harmonization-with-New-SDS-Safety-Data-Sheet-Format-505972/MARCH-2018-ES-TRAININGREGISTRY
  • 6 Request Info

    Webinar On Garnishments, Subpoenas, Summonses, and Levies update 2017

    Garnishments are a requirement of doing business and managing employees but juggling the requirements of different types of garnishments and federal and state laws can be exhausting. This webinar with expert Dayna Reum will give you the tips and tools to know how to stay compliant and process garnishments accordingly for 2017.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/HANDLING-DOCUMENTS-BACK-OFFICE-505862/AUGUST-2017-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 Lyophilization: What you need to Know, Validation and Regulatory Approaches

    More and more of today's (and tomorrow's) drugs are biotech drugs, complex and often highly sensitive molecules. External factors such as oxygen, sunlight, and pH values can negatively affect biotech products, leaving marketers looking for innovative ways to protect and preserve these important compounds until they can be administered to patients. The lyophilization process can protect biological activity, extend shelf life, and even increase dosing precision. In recent years, more than 30% of parenteral Food and Drug Administration (FDA) approvals were for lyophilized drugs, and estimates predict that soon more than half of all injectable drugs will require lyophilizationPrice:$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/LYOPHILIZATION-PROCESS-FDA-REGULATORY-508301/AUGUST-2017-ES-TRAININGREGISTRY
  • 9 Request Info

    Webinar On Cleaning Validation Guidelines

    This webinar discusses global Cleaning Validation Guidelines as they are currently available for pharmaceutical and biopharmaceutical industries. In addition, it describes use of QRM (quality risk management) in Cleaning Validation and growing trend of applying this approach to lifecycle of product manufacturing process. Establishing of health based Cleaning Validation limits also discussed in this session.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/CLEANING-VALIDATION-GUIDELINES-503490/AUGUST-2017-ES-TRAININGREGISTRY
  • 10 Request Info

    Webinar On The Risk Assessment Approach to Safety in the Workplace

    Risk Assessment is the central concept of modern health and safety. It is the tool that allows organizations to make informed decisions on how to protect the safety of their employees and other people without the need for prescriptive controls from outside bodies. This webinar will explain how to carry out a risk assessment for your own workplace.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/RISK-ASSESSMENT-SAFETY-WORKPLACE-509913/AUGUST-2017-ES-TRAININGREGISTRY
  • 11 Request Info

    Webinar On Bad Standard Operating Procedures (SOPs) = Bad Training: Garbage In, Garbage Out

    Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical employees are required to perform. Still, it is not widely understood how the writing of a procedure can have a positive or negative impact on training. In this course you will learn the vital connection between the documentation and training spheres, and how to maximize this connection to improve the quality of both SOPs and training.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/BAD-STANDARD-OPERATING-PROCEDURES-SOPs-506264/AUGUST-2017-ES-TRAININGREGISTRY
  • 12 Request Info

    Webinar On ISO 9001:2015 Quality Management System: Preparing for a Successful Transition

    In this webinar our speaker Lena Cordie will train on how to carry out a gap analysis against the requirements of ISO 9001:2015 to make the transition smooth and transparent. This exercise will provide your organization with structured assistance to highlight the extent to which existing systems and controls cover the requirements of ISO 9001:2015, or to identify an implementation action plan, where needed.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/ISO-9001-2015-QUALITY-MANAGEMENT-SYSTEM-503857/JULY-2017-ES-TRAININGREGISTRY
  • 13 Request Info

    Webinar On Structuring IC-DISCs to Maximize Your Tax Benefits

    The interest-charge domestic international sales corporation (IC-DISC) tax incentive for manufacturers, producers, resellers and exporters of exported U.S.-manufactured products offers the opportunity to decrease federal income tax on a portion of exports by 20 percentage points. Now is the time to explore how different structuring opportunities can help an exporter implement an IC-DISC or to maximize its IC-DISC benefit.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/STRUCTURING-IC-DISCs-MAXIMIZE-TAX-BENEFITS-504166/JULY-2017-ES-TRAININGREGISTRY
  • 14 Request Info

    Webinar On An Introduction to Risks associated with Extractables, Leachables & Elemental Impurities in cGMP Manufacturing: A Project Managers Perspect

    This webinar will present a unique perspective on risks associated with extractables, leachables & elemental impurities (ELEI) in cGMP manufacturing of pharmaceutical, biologic and medical device products. The webinar will start with a definitional review of the topic and then present the current FDA perspective on impurities of these types in product. After that introduction, the instructor will present quality and compliance considerations related to ELEI.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/EXTRACTABLES-LEACHABLES-cGMP-MANUFACTURING-507103/JULY-2017-ES-TRAININGREGISTRY
  • 15 Request Info

    Webinar On Understanding and Implementing USP 1058 - Analytical Instrument Qualification

    This webinar is designed to provide both a regulatory compliant and practical overview of equipment/instrument qualification, including requirements associated with instrumental system validation. This is critical in meeting existing regulatory requirements and ensuring efficient and cost-saving quality measurements and operations. In addition to USP <1058>, this will review other related compliance requirements, along with a practical overview of establishing an effective and efficient equipment qualification 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/UNDERSTANDING-IMPLEMENTING-USP-1058-509092/JULY-2017-ES-TRAININGREGISTRY
  • 16 Request Info

    Webinar On Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based Approach

    This 90-minute training program is designed for people tasked with performing external audits for their organizations. It is also for those tasked with developing, maintaining and/or improving programs for manufacturing facilities. This includes individuals that have quality management system responsibilities for making general improvements in their organization's performance specifically related to equipment, processes and documentation.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/AUDITING-QUALIFYING-SUPPLIERS-VENDORS-504232/JULY-2017-ES-TRAININGREGISTRY
  • 17 Request Info

    Webinar On Strategic Planning and Execution: The 1-2-3 Year Plan for Enterprise Success

    Is your organization poised to implement strategies that create value, generate growth and result in profits? Who thinks strategically in your firm? Strategy formation and strategic thinking have evolved; make sure your strategic thinking skills are keeping pace. You need to know the answers to these questions plus, what tools still work and continue to be useful in the development of strategy. What new approaches might give your organization a kick-start to move to a new level of high performance?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/STRATEGIC-PLANNING-EXECUTION-507002/JULY-2017-ES-TRAININGREGISTRY
  • 18 Request Info

    Webinar On OSHA's Fall Protection Safety Best Practices: Understanding the Changing Requirements for General Industry and Construction

    This online training course follows OSHA requirements for fall protection training for the construction worker who might be exposed to fall hazards. This program enables the employee to recognize the hazards of falling, and trains them in the procedures to be followed to minimize these hazards. With falls from heights being the leading cause of occupational fatalities, it is not only imperative that employers train their employees; it is also mandated by law, CFR 1926.503.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/OSHAs-FALL-PROTECTION-SAFETY-506072/JULY-2017-ES-TRAININGREGISTRY
  • 19 Request Info

    Webinar On Excel Spreadsheets: Develop and Validate for 21 CFR Part 11 Compliance

    Spreadsheets are powerful business tools, and are increasingly used in manufacturing, tracking and quality systems - as well as in generating and interpreting business data. FDA requires spreadsheets to be validated per 21 CFR 210-211, Part 820 and to be compliant to 21 CFR Part 11 in some cases.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/EXCEL-SPREADSHEETS-502490/JULY-2017-ES-TRAININGREGISTRY
  • 20 Request Info

    Webinar On Creating a Good Design History File (DHF) for Audit Success

    This webinar will cover the basics on how to maintain a good Design History File (DHF) that will help a manufacturer in a regulatory compliance audit. The webinar will cover the structure of a DHF and steps to ensure that the DHF is completed as the design and development process progresses. The DHF needs to be maintained as design changes are performed. Information in the DHF can help facilitate design decisions, which often can affect the safety of the device. The DHF provides the knowledge base needed for the manufacturer to maintain the device. It also provides the secrets to a successful Design Control audit.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-DESIGN-HISTORY-FILE-AUDIT-506688/JULY-2017-ES-TRAININGREGISTRY