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Enhancing Clinical Research: Optimizing Vendor Selection and Oversight from a GCP Perspective 

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In the realm of clinical research, the selection and management of vendors are pivotal to the success and integrity of clinical trials. Adhering to Good Clinical Practice (GCP) guidelines, a cornerstone in ensuring the ethical and scientific quality of clinical studies, is essential. This article delves into optimizing vendor selection and oversight within clinical research through a GCP lens, aiming to provide insights and strategies that bolster trial success while upholding stringent GCP standards. 

Understanding GCP Guidelines in Vendor Management GCP guidelines offer a comprehensive framework for conducting clinical trials, encompassing aspects from planning to execution and reporting. In vendor selection and oversight, these guidelines emphasize the importance of vendor competence, reliability, and adherence to regulatory requirements. Understanding these guidelines is crucial for clinical research organizations to ensure their vendors align with GCP principles, thus safeguarding study integrity and participant safety. 

Strategic Vendor Selection The process of selecting the right vendor is critical. It begins with defining clear criteria based on GCP requirements, which include technical expertise, regulatory compliance, and experience in clinical research. Assessing potential vendors against these criteria through a rigorous evaluation process ensures that only those with proven track records in GCP adherence are considered. This approach minimizes risks and lays a solid foundation for successful clinical trial execution. 

Effective Vendor Oversight Once vendors are selected, establishing robust oversight mechanisms is key to maintaining GCP compliance throughout the clinical trial lifecycle. This involves regular monitoring, performance reviews, and ensuring continuous alignment with GCP standards. Effective oversight also includes fostering open communication channels, enabling quick resolution of issues, and facilitating continuous improvement in vendor services, all within the GCP framework. 

Leveraging Technology in Vendor Management Technology plays a crucial role in enhancing vendor selection and oversight. Utilizing specialized software and platforms can streamline these processes, offering tools for better evaluation, monitoring, and communication. In a GCP context, technology can facilitate real-time oversight, improve documentation practices, and ensure more efficient and transparent vendor management processes. 

Fostering Collaborative Partnerships Building a collaborative partnership with vendors, grounded in mutual understanding and respect for GCP guidelines, is essential for optimizing outcomes. This collaboration should focus on shared goals, proactive communication, and joint problem-solving, ensuring that both parties are aligned in their commitment to upholding the highest standards of clinical research practice. 

Overall, optimizing vendor selection and oversight is a dynamic and critical component of conducting clinical research within the GCP framework. By adhering to GCP guidelines, employing strategic selection processes, implementing effective oversight, leveraging technology, and fostering collaborative partnerships, research organizations can enhance the quality and efficacy of clinical trials. These practices not only ensure compliance and safeguard participant welfare but also contribute to the robustness and credibility of research findings. 

Engage With Us How does your organization optimize vendor selection and oversight in alignment with GCP standards? Are there particular strategies or tools you find effective? We welcome your insights and experiences, encouraging a collaborative dialogue to advance our shared goal of excellence in clinical research. 

In adopting these strategies, organizations can navigate the complexities of vendor management in clinical research, ensuring that every partnership and process is conducive to high-quality, GCP-compliant study outcomes. 

A Guide to Enhancing Your Vendor Auditing Skills 

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In an era where vendor partnerships are integral to business success, understanding the nuances of vendor auditing is crucial. This guide aims to empower our free subscribers with foundational knowledge and actionable insights to elevate your vendor auditing capabilities, ensuring you are equipped to contribute effectively to your organization’s vendor management strategy. 

Understanding Vendor Auditing
Vendor auditing is a systematic process to assess a vendor’s compliance with contractual agreements, industry standards, and regulatory requirements. It helps identify risks, uncover inefficiencies, and foster improvement. For any professional eager to refine their auditing acumen, grasping these basics is the first step toward deeper engagement with advanced auditing practices. 

Core Elements of Vendor Auditing 

  • Compliance Checks: Learn to verify that vendors meet all contractual obligations and adhere to relevant laws and regulations. 
  • Performance Assessment: Understand how to evaluate the quality of goods or services provided, focusing on consistency, reliability, and value. 
  • Risk Identification: Grasp the basics of identifying potential risks associated with vendor partnerships, including financial, operational, and reputational risks. 

Building Your Auditing Toolkit

  • Documentation Review: Master the art of scrutinizing contracts, service level agreements (SLAs), and compliance certificates. 
  • Interview Techniques: Develop skills to effectively interview vendor representatives, extracting candid insights and valuable information. 
  • Observational Audits: Learn the essentials of conducting site visits or virtual audits to observe vendor operations firsthand. 

Best Practices for Effective Auditing 

  • Establish clear objectives for each audit. 
  • Maintain impartiality and objectivity throughout the auditing process. 
  • Develop a systematic approach to documenting findings and recommendations. 

While this guide provides a solid foundation, continuous learning and practice are key to mastering vendor auditing. Stay engaged with our content, explore case studies, and participate in discussions to further your understanding and skills. 

We value your feedback and experiences. Share your vendor auditing stories or questions with our community to foster shared learning and growth. 

 

 

 

Mastering Inspection Readiness: A Strategic Approach

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In the constantly shifting terrain of regulatory compliance, mastering inspection readiness is more crucial than ever. Central to this challenge is developing and implementing a robust Inspection Readiness Plan (IRP). This plan isn’t just a procedural necessity; it’s a strategic asset aligning resources, processes, and teams toward ensuring successful regulatory adherence.

Strategic Inspection Readiness Planning
• Blueprint for Success: An IRP serves as a comprehensive framework, not just a checklist. It outlines the inspection’s scope, identifies key focus areas, and sets clear objectives. The plan is a navigational tool guiding teams through compliance complexities, addressing potential challenges proactively.
• Resource Alignment: It strategically aligns an organization’s resources, ensuring that all elements work in harmony towards the common goal of compliance.

Collaborative Execution
• Unified Efforts: The effectiveness of an IRP hinges on collaboration across various departments. Each department contributes its expertise, ensuring comprehensive compliance coverage.
• Responsibility Sharing: This collaborative approach evenly distributes responsibilities and fosters a unified response strategy.

Data Management and Transparency
• Clear Data Insights: At the heart of the IRP is data management. Organized and accessible data is vital for setting accurate inspection criteria, identifying compliance gaps, and implementing corrective actions.
• Informed Decision Making: Effective data management provides a transparent view of the organization’s compliance status, enabling informed and timely decisions.

Digital Tools: Enhancing Efficiency
• Streamlining Processes: Integrating digital tools into the IRP enhances its efficiency. These tools aid in data collection, document management, and real-time compliance monitoring.
• Reducing Error: Digital tools simplify complex processes, minimize manual errors, and ensure that compliance information is readily accessible.

Constant State of Readiness
Dynamic Adaptability: A well-executed IRP maintains an organization in a constant state of readiness, prepared for both scheduled and unexpected inspections. The plan should be flexible, reflecting the latest regulatory requirements and industry best practices.

Continuous Improvement Cycle
• Learning and Adapting: The IRP is part of a continuous improvement cycle, learning from each inspection and adapting processes    accordingly.
• Staying Ahead: This approach ensures that the organization stays ahead of regulatory changes and incorporates lessons learned into future readiness strategies.

Cultivating a Culture of Compliance
• Excellence and Quality: An effective IRP fosters a culture where quality and compliance are integral to every process and decision.
• Community Engagement: How is your organization nurturing this culture of excellence and compliance?

Conclusion: Your Role in Shaping Compliance
As we navigate the future of regulatory compliance, the significance of a well-crafted IRP is undeniable. It symbolizes a commitment to excellence, quality, and adaptability. Your experiences and insights are pivotal in enriching this dialogue and fostering a culture of shared learning and continuous improvement.


Join the conversation on how to master the art of inspection readiness. Your perspectives are key in shaping effective compliance strategies and navigating the future of regulatory compliance. For further insights, explore our related article on “Why Quality is Everyone’s Business.”

A New Era: AI, Decentralized Trials, and Regulatory Compliance

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In this article, we delve into the intricacies of the evolving landscape of clinical research in 2024 with Artificial Intelligence (AI), Decentralized Clinical Trials (DCTs), and regulatory compliance.

The AI Revolution in Clinical Research
Artificial Intelligence (AI) is no longer just a buzzword in the realm of clinical research; it’s a reality reshaping our approach towards drug discovery and development. The integration of AI in this field has brought about unprecedented efficiency and precision. AI’s capability to analyze vast datasets is not only accelerating the process of identifying potential drug candidates but also ensuring that these candidates are more tailored and effective.

This technological advancement extends beyond just drug discovery. AI is revolutionizing manufacturing processes, enabling us to monitor and analyze extensive datasets. This oversight is crucial in enhancing production procedures, minimizing waste, and upholding rigorous quality control standards. The result? A more efficient, cost-effective, and quality-driven manufacturing process.

Decentralized Trials: A Patient-Centric Approach
Decentralized Trials (DCTs) are another pivotal trend in 2024. By shifting clinical trials from traditional, centralized locations to virtual or remote environments, DCTs are making clinical research more accessible and inclusive.

This shift is crucial in addressing the historical challenges of patient recruitment and retention. DCTs allow for broader demographic participation, offering insights into diverse patient experiences and responses to treatments.

However, the rise of DCTs also brings forth new challenges. Ensuring data integrity, managing patient privacy, and maintaining rigorous regulatory compliance in a decentralized setting require innovative solutions and strategic foresight.

Regulatory Compliance: A Moving Target
In this rapidly evolving environment, regulatory compliance remains a critical focus. The landscape is shifting, with regulatory bodies like the FDA placing greater emphasis on data integrity, sponsor oversight, and risk management. It is more important than ever for organizations to stay abreast of regulatory changes and ensure compliance.

The focus is not just on meeting current standards but anticipating future regulations. Engaging with Quality Assurance (QA) teams and leveraging their expertise in mock inspections and preparation can be a game-changer. Organizations must also be proactive in understanding and implementing the latest guidelines to maintain inspection readiness.

The Road Ahead
As we move forward in 2024, the clinical research landscape will continue to evolve. The integration of AI and the rise of DCTs are just the tip of the iceberg. We’re heading towards a more patient-centric, data-driven, and efficient era of clinical research.

But this journey is not without its challenges. Balancing technological advancement with ethical considerations, data integrity, and regulatory compliance is key. It’s an exciting time to be part of this industry, and we’re here to navigate these changes together.

Your Role in Shaping the Future
As valued members of our community, your insights and experiences are crucial in shaping the future of clinical research. We encourage you to engage with these topics, share your perspectives, and be a part of the conversation.

Together, let’s redefine the boundaries of clinical research and usher in a new era of innovation and excellence.

Inspection Readiness Outlook 2024: Navigating FDA Expectations in the Clinical Industry

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As the clinical industry ventures into 2024, the landscape is increasingly shaped by the FDA’s evolving expectations. This year, a greater emphasis is placed on data integrity, technological integration, and the adaptation to new inspection models. In this context, insights from previous blogs such as “Why Quality is Everyone’s Business“, “Steps To Establishing a Quality Culture in Clinical Research“, and “How Changes in E6 (R3) of ICH GCP are Changing the Future of Clinical Trials” become particularly relevant.

  1. Emphasizing Quality as a Universal Responsibility

Echoing the sentiments of “Why Quality is Everyone’s Business“, it’s imperative to recognize that quality in clinical trials is not just the responsibility of the quality assurance team but of every individual involved. This collective approach ensures thorough preparation for FDA inspections and enhances overall trial integrity.

  1. Establishing a Quality Culture in Clinical Research

Drawing from “Steps To Establishing a Quality Culture in Clinical Research”, it is crucial for organizations to cultivate a culture where quality is ingrained in every process. This involves regular training, proactive risk management, and an environment that encourages transparency and continuous improvement. Such a culture not only aids in inspection readiness but also ensures adherence to the highest standards of clinical research.

  1. Adapting to Changes in ICH GCP Guidelines

The blog “How Changes in E6 (R3) of ICH GCP are Changing the Future of Clinical Trials” highlights the significant updates in the ICH GCP guidelines, especially E6 (R3). These changes, focusing on risk-based approaches and enhanced data integrity, have direct implications on inspection readiness. Organizations need to adapt their strategies and processes to align with these updated guidelines, ensuring compliance and readiness for FDA inspections.

  1. Integrating Technology and Data Management

With the FDA’s technology-driven approach, organizations must integrate advanced data management systems and adopt technologies like AI and blockchain for better traceability and security. This also includes ensuring that electronic health records (EHRs) and electronic data capture (EDC) systems are leveraged effectively for streamlined data collection and analysis.

  1. Remote and Hybrid Inspection Readiness

Adapting to remote and hybrid inspection models is essential. Organizations must ensure their digital infrastructure is secure, compliant, and capable of providing necessary documentation and data remotely.

  1. Global Regulatory Compliance

For organizations involved in international trials, understanding and adhering to global regulatory standards, including those set by the FDA, is crucial.

Conclusion

As the clinical industry progresses through 2024, a multifaceted approach to inspection readiness is key. Emphasizing quality as a collective responsibility, establishing a strong quality culture, adapting to changing guidelines, and leveraging technology are integral components of this strategy.

We Value Your Input:

How have the changes in ICH GCP guidelines impacted your organization’s approach to inspection readiness? Share your experiences and insights, and let’s discuss how these evolving standards are shaping the future of clinical trials.

Clinical Trial Trends in 2024: Innovations and Evolutions in Inspection-Readiness

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The year 2024 has brought significant innovations to the clinical trial sector, especially in terms of inspection-readiness. This article provides an overview of how these trends are influencing preparedness for regulatory inspections. For a deeper understanding of the importance of quality in this evolving landscape, read “Why Quality is Everyone’s Business“.

Technological Advancements in Inspection-Readiness

Technological integration is at the forefront of enhancing inspection-readiness. Digital documentation systems and AI-driven compliance tools are now vital in streamlining the inspection process. These technologies ensure continuous compliance and readiness, significantly reducing the risk of non-compliance during inspections. For practical insights into establishing an effective training program in this area, consider “Tips on Establishing an Inspection Readiness Training Program“.

Real-Time Data Monitoring

A notable trend is the adoption of real-time data monitoring systems. These systems provide ongoing oversight, immediately identifying and addressing areas of concern. This proactive approach ensures that trials maintain high standards of data integrity and regulatory compliance.

Decentralized Trials: Challenges and Solutions

The rise of Decentralized Clinical Trials (DCTs) poses unique inspection-readiness challenges. The article discusses strategies to ensure DCTs maintain the same level of regulatory compliance as traditional trials, focusing on remote monitoring and digital data validation methods.

Evolving Regulatory Expectations

Regulatory bodies are continuously evolving their expectations in response to these technological advancements re-shaping the future of clinical trial inspections.

Adapting to New Standards

Pharmaceutical companies and CROs are adapting their strategies to meet these new standards. Emphasis is placed on training, technology integration, and developing robust internal audit systems to ensure continuous inspection readiness. Explore the importance of establishing a quality culture in this context through “The Benefits of Establishing a Quality Culture In Clinical Operations“.

In conclusion, 2024 has marked a pivotal year in reshaping how clinical trials prepare for inspections. The trends discussed here highlight the industry’s move towards more efficient, technology-driven approaches to meet evolving regulatory standards.

Your Opinion Matters

What do you think will be the next big innovation in clinical trial inspection-readiness?

 

 

 

Clinical Trial Trends in 2024: Innovations and Evolutions in Inspection-Readiness

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As we navigate through the new year of 2024, the clinical trial landscape is experiencing transformative changes, particularly in the aspect of inspection-readiness. This abbreviated article provides a focused look into how these changes are influencing trial preparedness for regulatory inspections.

  1. Advancements in Inspection-Readiness The integration of new technologies and methodologies has brought about a significant shift in how clinical trials prepare for inspections. Innovations such as digital documentation systems and AI-driven compliance tools are streamlining the process, ensuring trials are always inspection-ready.
  2. Real-Time Data Monitoring The adoption of real-time data monitoring systems is a game-changer. These systems provide continuous oversight of trial data, flagging inconsistencies and areas of concern well before an inspection, thus reducing the risk of non-compliance.
  3. Decentralized Trials and Inspection Challenges Decentralized clinical trials (DCTs), while offering numerous benefits, also present unique challenges in maintaining inspection-readiness. Our article discusses strategies to overcome these challenges, ensuring DCTs adhere to regulatory standards effectively.

Conclusion The full article, accessible to our subscribers, delves deeper into how these trends are reshaping inspection-readiness in clinical trials and explores the evolving regulatory expectations and how companies are adapting to meet these new standards.  🔗 Subscribe now for full access to in-depth insights.

Your Insight Counts How do you think technology will further impact inspection-readiness in clinical trials beyond 2024?  Let us know in the comments section.  We look forward to hearing from you!

Why Quality is Everyone’s Business

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World Quality Day, celebrated on a global scale every year on the second Thursday in November, serves as a reminder that quality is not just a buzzword or a department in your organization—it’s everyone’s business. Whether you work in clinical operations, healthcare, manufacturing, or any other industry, ensuring quality should be a shared responsibility. In this blog post, we’ll explore why quality is crucial, how it impacts various aspects of your business, and why fostering a culture of quality is essential for long-term success. 

Quality Breeds Trust

Quality is the cornerstone of trust. When you consistently deliver high-quality products or services, your customers and clients develop trust in your brand. Trust is not just important for customer satisfaction but also for building lasting relationships. In clinical operations, trust is paramount, as patients rely on healthcare professionals to provide accurate diagnoses and effective treatments. The link between trust and quality is evident, making it clear that quality is everyone’s responsibility.

Quality Enhances Efficiency

Poor quality can lead to inefficiencies, causing wasted time and resources. When a product or service lacks quality, it often requires rework, leading to increased costs and delays. By prioritizing quality, each team member can contribute to streamlined processes, reducing errors, and boosting productivity. In clinical operations, efficiency can save lives, making the pursuit of quality a shared mission.

Quality Reduces Risk

Quality control and risk management go hand in hand. Ensuring high-quality products or services minimizes the potential for defects, recalls, or adverse events. In clinical operations, such as drug development, the consequences of poor quality can be catastrophic. By making quality everyone’s business, organizations can proactively identify and mitigate risks, safeguarding the well-being of patients and the reputation of the company.

Quality Drives Innovation

Innovation and quality are interconnected. When every team member is committed to delivering high-quality results, they’re more likely to seek creative solutions and improvements. Quality-driven innovation can lead to better products, services, and processes, setting your organization apart from the competition. In clinical operations, innovation can lead to groundbreaking treatments and advancements in patient care.

Quality Fosters a Culture of Excellence

A culture of quality doesn’t happen by chance; it’s a result of collective effort. When quality is everyone’s business, it becomes a part of your organization’s DNA. This shared commitment to excellence encourages employees to take pride in their work and continuously strive for improvement. In clinical operations, a culture of quality can save lives and contribute to the development of groundbreaking treatments.

In conclusion, quality is not a solitary responsibility but a collective one. From the boardroom to the front lines, everyone plays a vital role in ensuring quality. By fostering a culture where quality is valued and upheld by all, organizations can build trust, enhance efficiency, reduce risk, drive innovation, and ultimately achieve long-term success.

Now that we’ve established that quality is everyone’s business, it’s time to take action. The success of your clinical operations depends on a collective commitment to quality. As we acknowledge WORLD QUALITY DAY, let’s make a collaborative effort to act on the principles discussed in this article. Implement a culture of quality within your clinical operations. Start discussions within your team, set quality benchmarks, and continuously strive to exceed them. Remember, quality is not a destination but a journey, and it’s a journey that’s everyone’s business.

Together, we can build a future where the quality of our work is synonymous with the quality of life for countless patients. It’s a journey worth taking, and it starts with you.

Take the First Step towards Quality Excellence

Quality is not a department. It’s not a job title. It’s a mindset, a commitment, and a culture. Make it everyone’s business, and you’ll be one step closer to achieving excellence in clinical operations. So, let’s celebrate World Quality Day by embracing quality as everyone’s business, and don’t forget to join our mailing list and subscribe to our newsletter for regular quality insights and updates.

Tips on Establishing an Inspection Readiness Training Program

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The task of documenting and maintaining records can prove to be a daunting one in the world of clinical research.  Effective resource allocation constitutes a delicate equilibrium. Striking the right balance between dedicating resources to training and compliance initiatives while judiciously managing costs becomes an intricate endeavor for organizations. It is critical to be attentive to resource needs in addition to ensuring that employees receive comprehensive inspection-readiness training in preparation for health authority inspections.  The do’s and don’ts of inspection readiness training that contributes to readiness success includes the following:

Do:

  1. Consistent Training Plan – Establish a regular schedule for training sessions, ensuring that all team members acquire a comprehensive understanding of health authority regulations and adherence to documented standard operation procedures.
  2. Exemplary documentation standards – Stress the importance of meticulous and comprehensive documentation. Implement and practice the most effective methods for maintaining impeccable records.
  3. Comprehensive cross-training – Promote cross-functional training initiatives aimed at nurturing a corporate culture deeply ingrained in compliance across various departments within your organization’s structure.
  4. Realistic scenario simulations – Create mock inspection scenarios that closely resemble real-world situations. This valuable exercise will help identify weaknesses and areas in need of improvement.
  5. Proactive regulatory awareness – Continuously monitor and stay informed about regulatory updates, adjusting your training programs to align with these evolving regulations.

Don’t:

  1. Discount the gravity of compliance – Never underestimate the gravity of aligning with regulations. Forgoing due diligence or shortcutting compliance requirements can result in grievous regulatory issues.
  2. Neglect training documentation – Never depreciate the importance of documenting training, both in terms of accuracy and completeness. Neglecting to properly oversee and document training can furnish a breeding ground for critical compliance and data discrepancies.
  3. Neglect post-training reinforcement – The failure to revisit training and scrutinize employee compliance can vitiate the efficacy of the training initiative. Assure that senior leadership exudes unwavering commitment to the training program.
  4. Defer compliance or cultivate a culture of blame – Do not defer the serious consideration of compliance until impending regulatory inspections materialize. Shun the cultivation of a culture that lays blame upon employees who are may not be main contributors to the errors or data discrepancies.
  5. Underestimate resource allocation – Do not underestimate the resource allocation requirements for the efficacious execution of training and compliance endeavors. Insufficient resource allotment can enervate the quality of training and impede compliance endeavors.

In conclusion, maintaining inspection readiness is a continuous process that demands diligence, commitment, and a robust training program. The challenges posed by evolving regulations and complex documentation can be overcome by following the dos and don’ts outlined above. By investing in comprehensive inspection readiness training program, organizations can safeguard their reputation, product quality, and, most importantly, patient safety in an ever-evolving regulatory landscape.

If you need to develop an inspection-readiness training program and need assistance, Contact us for a free consultation! We would love to hear from you to discuss strategies!

5Cs to Inspection Readiness Success (for Clinical Sites)

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By the 2K Blog /team

Q: When is the best time to start preparing for an inspection?   

    1. After database lock 
    2. After the inspection announcement 
    3. After IND/IDE Submission 

‎A: If you answered C, you are correct. ‎‎ ‎‎ ‎‎Inspection Readiness is an ongoing process that starts at the beginning of the trial. ‎

We all know that inspections can be quite stressful; however, a stressful environment can be minimized with proper preparation and inspection readiness techniques.  This article will discuss the 5C IRS (Inspection Readiness Success) Model as one of the strategies that can be utilized as an inspection readiness technique for clinical research sites.

The 5Cs are: 

  1. Collect Information – In collecting information, it’s important to consider researching from both internal sources (e.g., prior audits, inspections and monitor visit reports) to determine existing gaps in your processes in addition to external sources (e.g., websites of regulatory authorities such as USFDA, EMA, Health Canada, etc.) to review guidance materials, requirements and expectations.

  2. Collaborate with the sponsor – Be proactive in utilizing inspection readiness tools and collaborating with the monitor & sponsor’s inspection team for additional support in preparing for inspections and implementing effective inspection readiness strategies.

  3. ‎Communicate with stakeholders‎‎ – ‎‎Communicate with internal stakeholders (colleagues, PI, monitor) to address gaps in study-related documentation to ensure that they‎‎ ‎‎are present, ‎‎complete‎‎ and accurate.‎‎ ‎‎ ‎‎ I‎‎t’s equally important to ensure that staff are properly prepared to communicate with external stakeholders (e.g., regulatory authorities) and able to interact ‎‎effectively ‎‎with the Inspector/FDA Investigator prior to, during and after the inspection.‎‎ ‎‎ ‎‎ ‎

  4. Correct via CAPA (Corrective and Preventive Action) Plans – Part of having an effective Corrective and Preventive Action plan for each finding is to include all of the elements such as:

    • Root Cause – Why did this happen? Was it a systemic or isolated event? 
    • Correction – What correction was done to immediately resolve this finding?
    • Corrective Action – What will be your corrective action and how will you implement to ensure this finding does not recur?  For example, you may need to create, improve, revise SOPs and checklists/templates and retrain staff on the revised processes.
    • Preventive Action – What are you checks and balances?  Incorporate preventive measures within a timeframe (e.g., 3- 6 months) to ensure similar finding(s) never happens again.

       

  5. Conduct Compliance Checks – Compliance checks involve the evaluation of the implemented processes from your CAPA.   Utilize checklists at frequent intervals to reveal gaps and determine what’s working vs. what’s not.  In addition, review findings from monitoring visits as gauge for compliance checks especially if time and resources are limited at your clinical research site.

Remember, inspection readiness is an ongoing process.  Incorporating an Inspection Readiness strategy, such as the 5C IRS (Inspection Readiness Success) Model, in your daily operations not only creates a culture of compliance, but also allows your site to proactively prepares for and contributes to the success of future inspections.  

Need a checklist for your site? Become a subscriber to download our free Inspection Readiness Checklist!

 

 

Our Mission and Purpose

The mission of 2K Clinical Consulting, Inc. is to ease the burden of GxP compliance and to transform the effectiveness of professionals and compliance systems worldwide.

Our History

2K Clinical Consulting, Inc. is the vision of former FDA Investigator, Kimberly Kiner, who empathized with facilities and sites that struggled with understanding and complying with regulations. After years in the field, Kimberly transitioned into the private sector and acquired international experience in compliance, monitoring and study management while she worked for pharmaceutical and invitro/medical device companies as well as CROs. This work experience is what sparked her desire to work as a consultant for organizations such as the Association for Clinical Research Professionals and the Society of Clinical Research Associates. Kimberly later went on to train providers such as Compliance Online and Fx Conferences. This exposure became the gateway to connecting with other experts and teaching professionals resulting in an engaging experience for clients that closes the gap in best practices within the realm of compliance.