SOPs - How to Write Them to Satisfy Those Inspectors

  • Tuesday
  • August
  • 6
  • 2024
10:00 AM PDT | 01:00 PM EDT
90 Minutes
Meredith Crabtree Instructor:
Meredith Crabtree 
Webinar Id:

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Price Details
$149 Live
$299 Corporate Live
$199 Recorded
$399 Corporate Recorded
Combo Offers
Live + Recorded
$299 $348 Live + Recorded
Corporate (Live + Recorded)
$599 $698 Corporate
(Live + Recorded)
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Attending this training will help the participant understand the specific requirements and expectations of FDA inspectors, allowing them to develop SOPs that meet regulatory standards and demonstrate compliance.

By learning how to write SOPs that satisfy FDA inspectors, participants can proactively identify and address potential compliance gaps or issues. This training will provide them with the knowledge and skills necessary to develop robust and comprehensive SOPs, minimizing the risk of regulatory non-compliance and associated penalties.

Effective SOPs not only satisfy FDA inspectors but also contribute to improved operational efficiency and consistency within an organization. By attending this training, one will learn how to write SOPs that clearly outline procedures, roles, and responsibilities, promoting standardized processes and reducing variability in operations.

Well-written SOPs provide clear instructions on how to perform tasks correctly and safely. By attending this training, participants will gain insights into developing SOPs that prioritize quality and safety, aligning with FDA's expectations. This can help mitigate risks, reduce errors, and ensure product quality and patient safety.

Why should you Attend: Unlock the keys to regulatory success with our dynamic training program, "Mastering SOPs for Regulatory Compliance." In the world of FDA-regulated industries, Standard Operating Procedures (SOPs) are the foundation upon which compliance and operational excellence stand. Join us for an immersive experience that goes beyond conventional training, providing professionals with the insights, best practices, and practical skills needed to navigate the complexities of SOP development, implementation, and maintenance.

This comprehensive program is strategically crafted to address the critical role that SOPs play in regulatory compliance. SOP deficiencies consistently rank among the top findings in FDA audits, posing significant risks to an organization's Quality Management System (QMS) and potentially leading to severe consequences. Our training aims to empower professionals with the knowledge to not only avoid common pitfalls but also to elevate SOPs as strategic tools for ensuring completeness, accuracy, and consistent adherence to regulatory standards.

Key Highlights:

  • Regulatory Landscape Insight:
    • Gain a profound understanding of the regulatory expectations surrounding SOPs, ensuring that your organization is well-prepared to demonstrate compliance during inspections
  • Real-world SOP Deficiencies Analysis:
    • Explore real-life examples and case studies to identify the top 5 SOP deficiencies encountered during FDA audits. Learn from these scenarios to fortify your organization against similar pitfalls
    • Best Practices in SOP Development:
    • Receive expert guidance on crafting SOPs that are not only clear and effective but also align with regulatory requirements. Understand the collaborative approach necessary for comprehensive SOP development
  • Ensuring Completeness and Accuracy:
    • Acquire practical techniques for reviewing and enhancing existing SOPs, ensuring that they accurately reflect current processes and comply with evolving regulatory standards
  • Consistent Implementation Strategies:
    • Dive into strategies for fostering a culture of consistent SOP implementation across all levels of your organization. Understand the pivotal role of ongoing training in maintaining compliance
  • Risk Mitigation and Continuous Improvement:
    • Develop a proactive approach to risk identification and mitigation within SOPs, safeguarding your organization against potential compliance issues. Embrace a culture of continuous improvement to keep SOPs dynamic and effective
  • Benefits of the Training
    • Audit Preparedness: Arm your organization with the knowledge and tools to minimize SOP-related findings during regulatory inspections, reducing the risk of negative audit outcomes
    • Operational Confidence: Build confidence in your team's ability to develop and maintain SOPs that not only meet regulatory requirements but also contribute to operational excellence
    • Risk Resilience: Implement measures to proactively identify and address risks within SOPs, ensuring that your organization is resilient to potential regulatory challenges
    • Sustainable Compliance: Foster a culture where compliance is not just a checkbox but an integral part of everyday operations. Ensure that SOPs serve as dynamic tools for continuous regulatory adherence

Areas Covered in the Session:
  • Overview of the importance of SOPs in FDA-regulated industries
  • Overview of FDA regulations applicable to SOPs (e.g., 21 CFR Part 211, 21 CFR Part 820)
    • Key elements and requirements for SOPs according to FDA expectations
  • Appropriate Outline and Format of SOPs
    • Appropriate use of terminology
    • Identify the audience
    • Use of Process Maps, Pictures, Diagrams, If/ Then charts, etc.
  • Common Deficiencies and Pitfalls
  • How to Mistake proof SOPs through use of Industry Best Practices and Agency expectations
  • General Overview of Document Control and how to put it into practice
  • FDA expectations on SOP training

Who Will Benefit:
  • Quality Assurance (QA) Department:
    • QA Managers
    • QA Specialists
    • QA Analysts
  • Regulatory Affairs Department:
    • Regulatory Affairs Managers
    • Regulatory Affairs Specialists
    • Compliance Officers
  • Manufacturing and Production Department:
    • Manufacturing Managers
    • Production Managers
    • Operations Managers
  • Research and Development (R&D) Department:
    • R&D Managers
    • R&D Scientists
    • Product Development Specialists
  • Clinical Research Department:
    • Clinical Research Managers
    • Clinical Research Associates
    • Clinical Trial Coordinators
  • Validation Department:
    • Validation Managers
    • Validation Engineers
    • Validation Coordinators
  • Quality Control (QC) Department:
    • QC Managers
    • QC Analysts
    • QC Technicians
  • Compliance Department:
    • Compliance Managers
    • Compliance Specialists
    • Regulatory Compliance Officers
  • Medical Affairs Department:
    • Medical Affairs Managers
    • Medical Writers
    • Medical Information Specialists
  • Laboratory Department:
    • Laboratory Managers
    • Laboratory Technicians
    • Analytical Chemists
  • Risk Management Department:
    • Risk Managers
    • Risk Analysts
    • Patient Safety Officers
  • Supply Chain and Logistics Department:
    • Supply Chain Managers
    • Logistics Managers
    • Distribution Specialists
  • Clinical Operations Department:
    • Clinical Operations Managers
    • Clinical Operations Specialists
    • Study Coordinators
  • Complaint Handling and CAPA Teams:
    • Complaint Handling Managers
    • CAPA Coordinators
    • Corrective and Preventive Action Teams
  • Pharmacovigilance Department:
    • Pharmacovigilance Managers
    • Drug Safety Specialists
    • Adverse Event Coordinators
  • Infection Control Department:
    • Infection Control Managers
    • Infection Preventionists
    • Healthcare Epidemiologists
  • Auditing and Inspection Department:
    • Internal Auditors
    • External Auditors
    • FDA Inspectors
  • Health and Safety Department:
    • Health and Safety Managers
    • Occupational Health Specialists
    • Environmental Health Officers
  • Documentation and Recordkeeping Department:
    • Document Control Managers
    • Records Management Specialists
    • Document Compliance Officers

Speaker Profile
Meredith L. Crabtree has over 30 years’ experience in regulated industries, ranging from Blood, Plasma, Tissue, Laboratory, Pharma, Medical Device, Cosmetics, Supplements, and Animal Health. This includes manufacturing, packaging, labelling and distribution operations. Meredith is the owner of MLKC Consulting is s a Quality Consultant specializing in product label reviews, 3rd party inspections, Consent Decree and Recall support. She also performs regulatory assessments and Quality trainings.

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