Duration: 90 Minutes


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In today's rapidly evolving regulatory landscape, organizations across industries are under increasing pressure to ensure compliance with a multitude of laws, regulations, and industry standards. Compliance audits play a vital role in assessing an organization's adherence to these requirements, identifying potential risks, and implementing corrective measures.

Our upcoming webinar, "Compliance Audits Using Principles of Lean Documents and Lean Configuration," is designed to provide professionals with a deep understanding of the audit process, best practices, and strategies for effectively managing compliance obligations. Whether you're an auditor, compliance officer, or part of a company's governance team, this webinar offers invaluable insights to enhance your compliance program.

During this informative session, our expert speakers will delve into the key elements of a compliance audit and share practical tips to streamline your audit process. They will discuss the importance of establishing an audit framework tailored to your organization's specific compliance needs and outline the critical steps involved in planning, executing, and reporting on compliance audits.

Participants will gain knowledge on leveraging technology solutions to automate audit procedures, ensuring efficiency and accuracy in assessing compliance controls. Our speakers will explore emerging trends and innovative tools, such as data analytics and artificial intelligence, that can enhance audit effectiveness and enable proactive risk management.

Moreover, this webinar will highlight the significance of maintaining strong documentation practices and effective communication with stakeholders throughout the audit lifecycle. You'll learn how to establish robust internal controls, conduct comprehensive risk assessments, and develop remediation strategies to address audit findings efficiently.

Join us for the "Compliance Audits" webinar to equip yourself with the knowledge and tools necessary to navigate the complexities of compliance audits successfully. Our expert panelists will share their real-world experiences and provide practical guidance to help you stay ahead of regulatory requirements and safeguard your organization's integrity and reputation.

Don't miss this opportunity to gain valuable insights, network with industry peers, and enhance your compliance auditing skills. Register now to secure your spot in this transformative webinar that will empower you to master compliance audits and ensure a culture of compliance within your organization.

Why You Should Attend:

  • Enhance your knowledge: Compliance auditing is a critical aspect of any organization's governance framework. By attending this webinar, you will gain a comprehensive understanding of compliance auditing principles, methodologies, and best practices. This knowledge will enable you to strengthen your compliance program and contribute to your organization's overall risk management strategy.
  • Stay updated on regulatory requirements: The regulatory landscape is constantly evolving, with new laws, regulations, and industry standards being introduced regularly. By attending the webinar, you will stay up to date with the latest compliance requirements and understand how to align your organization's practices with these changes. This will help you avoid penalties, reputational damage, and legal liabilities.
  • Learn from industry experts: The webinar will feature expert speakers with extensive experience in compliance auditing. They will share their practical insights, case studies, and real-world examples, providing you with valuable guidance and actionable tips. Learning from experienced professionals will enhance your skills and enable you to apply industry-leading practices within your organization.
  • Streamline your audit process: Compliance audits can be complex and time-consuming. Attending the webinar will equip you with strategies and techniques to streamline your audit process, making it more efficient and effective. You will learn how to plan and execute audits, identify key risk areas, assess controls, and report on audit findings. These skills will help you conduct audits with confidence and achieve better results.
  • Leverage technology for auditing: Technology plays a crucial role in modern compliance auditing. The webinar will explore the latest technological advancements, such as audit management software, data analytics, and artificial intelligence. You will learn how to leverage these tools to automate audit procedures, analyze large volumes of data, and identify potential compliance gaps. Adopting technology in your auditing processes will enhance accuracy, reduce manual effort, and improve overall audit outcomes.
  • Compliance auditing is a systematic and independent assessment of an organization's adherence to regulatory requirements, internal policies, industry standards, and best practices. It involves reviewing and evaluating processes, controls, and documentation to ensure compliance with applicable laws and regulations.
  • Compliance audits aim to identify areas of non-compliance, assess the effectiveness of controls, and provide recommendations for improvement. The process typically involves planning and scoping the audit, gathering evidence through testing and interviews, analyzing findings, and reporting the results to management and relevant stakeholders.
  • Key areas covered in compliance audits may include data privacy, financial reporting, information security, anti-money laundering, environmental regulations, workplace safety, and more. The audit findings help organizations identify risks, strengthen controls, and demonstrate their commitment to regulatory compliance.
  • By conducting regular compliance audits, organizations can proactively identify and mitigate potential compliance gaps, reduce legal and reputational risks, and foster a culture of compliance throughout the organization. Compliance auditing plays a vital role in ensuring ethical practices, safeguarding stakeholder interests, and maintaining the integrity and trust of the organization.

Areas Covered in the Session :

  • Lean auditing techniques based on measurable deliverables
  • Comparing with the traditional compliance audit
  • Problem identification
  • Reporting format
  • Performance measurement
  • Effective follow up and verification strategies
  • How to immediately start implementing the methodology

Who Should Attend:

  • Quality Assurance Departments
  • Quality Control Departments
  • Regulatory Affairs Departments
  • Research and Development Departments
  • Manufacturing Departments
  • Engineering Departments
  • Operations Departments
  • Production Departments
  • Risk Management Professionals
  • Internal Auditors
  • Audit Committee Members

Course Director: José Mora

José Mora is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device and life sciences industry specializing in manufacturing, process development, tooling, and quality systems. Prior to working full time as a consulting partner for Atzari Consulting, José served as Director of Manufacturing Engineering at Boston Scientific and as Quality Systems Manager at Stryker Orthopedics, where he introduced process performance, problem solving, and quality system methodologies. During that time he prepared a white paper on the application of lean manufacturing methods to the creation and management of controlled documents and a template for strategic deployment.

José led the launch of manufacturing at a start-up urology products company as Director of Manufacturing for UroSurge, Inc. at the University of Iowa’s business incubator park in Coralville, IA, creating a world-class medical device manufacturing operation, with JIT, kanban systems, visual workplace and lean manufacturing practices. José worked for 10 years at Cordis Corporation, now a Cardinal Health company, where he led the successful tooling, process development and qualification of Cordis’ first PTA (percutaneous transluminal angioplasty) catheter.

His medical device experience includes surgical instruments, PTA & PTCA dilatation and guiding catheters, plastic surgery implants and tissue expanders, urology implants and devices for the treatment of incontinence, delivery systems for brachytherapy, orthopaedic implants and instruments, and vascular surgery grafts and textiles. During his time at Cordis, José managed the Maintenance and Facilities Department, taking that operation to a level rated as “tops” by the UK Department of Health and Social Services (DHSS) during one of their intensive audits. Jose managed Manufacturing Engineering as part of the Guiding Catheter Core Team of managers, a team that took the Cordis Guiding Catheter business to lead the market, bringing it up from fourth place. By introducing world-class techniques, the Guiding Catheter design and manufacturing was completely re-engineered for robust design and tooling, under José’’s leadership.

He was also instrumental and played a leadership role in the complete re-engineering of the Tooling Control System, including design drafting, the tool shop and technical support. Wherever he has worked, he has a track record of introducing world-class methodologies such as Kepner-Tregoe, Taguchi techniques, Theory of Constraints, Lean Manufacturing, Five S (Visual Workplace), process validation to Global Harmonization Task Force standards, and similar approaches.

Eventura World's refund policy applies to each product and service as detailed on the respective offering pages. If no specific refund policy is mentioned for an offering, the following general policy applies:

Cancellation by Registrant:
  • Registrants may cancel their registration for any reason up to 2 business days prior to the event. A refund will be issued minus a $45 administrative fee.
  • If a cancellation occurs after materials such as documents, handouts, checklists, slide deck, or recordings have been sent by Eventura, only 40% of the registration fee will be refunded.
  • If the registrant fails to cancel within the stipulated time or does not attend the event, no refund will be issued. Options available to the registrant in such cases include:
    1. Access to a one-time recording of the event.
    2. A redeemable voucher.
Substitutions of attendees may be made at any time by notifying Eventura via email.

Cancellation by Eventura:
  • Eventura reserves the right to cancel or reschedule an event due to insufficient registrations or unforeseen circumstances. Registrants will be notified via email prior to the event's start time unless prevented by situation beyond control.
  • If an event is rescheduled, registrants will be promptly informed of the new date and their registration will be automatically transferred.
  • If the new date is not suitable, registrants may choose from the following options:
    1. Access to a one-time recording of the webinar after the live session.
    2. A redeemable voucher valid for 12 months, applicable towards any future live event or past recording.
  • A full refund will be issued if no new date is provided within 90 days from the originally scheduled event date.
Event Cancellation:
If an event is permanently cancelled, registrants may opt for:
  • A recording of the webinar, if available.
  • A redeemable voucher.
  • A full refund.
Changes to Event Details:
Eventura reserves the right to modify some topics, materials, or speakers/instructors without prior notice.

Refund Processing:
Refunds are processed within 7 business days from the receipt of the refund request. Eventura World is not liable for any penalties or expenses incurred due to an event's cancellation.

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