A Cold Chain Process Validation Guide: Part 1: Introduction to Cold Chain Process Validation

A Cold Chain Process Validation Guide: Part 1: Introduction to Cold Chain Process Validation

Introduction

The integrity of cold chain management is pivotal in the demanding realm of pharmaceutical and biologic industries. This six-part article series explores Cold Chain Process Validation, addressing the multifaceted challenges and evolving demands professionals like yourself face in ensuring product integrity from manufacturing to delivery. Amidst economic, technological, and regulatory pressures, the series begins with an overview of the cold chain validation process, emphasizing the need for comprehensive strategies to navigate competing priorities, sustainability initiatives, and the globalization of supply chains.

The series continues with the critical aspects of cold chain management, from integrating management systems and developing mature quality systems for qualifying and validating equipment and processes essential for maintaining product quality. Each article builds upon the last, offering a detailed examination of operational qualification and the significance of performance qualification in affirming the effectiveness of cold chain management practices. The series encapsulates the essential elements required for a robust, compliant, and efficient cold chain, underscoring the importance of a lifecycle approach to process validation, integration of logistics, and innovative technologies.

Central to this comprehensive guide is the expertise of Modality Solutions, a frontrunner in cold chain management solutions for the pharmaceutical industry. Modality Solutions excels in navigating the complexities of the cold chain, providing invaluable insights into engineering, regulatory compliance, and quality assurance. Our proficiency and innovative approaches empower your company to enhance your cold chain systems, ensuring regulatory compliance, operational excellence, and the safe transport of products.

The series highlights the challenges faced by cold chain management professionals and showcases Modality Solutions’ commitment to delivering state-of-the-art solutions. We carve a path to achieving a compliant and efficient cold chain through practical examples and expert insights. Modality Solutions’ focus on simplifying complex cold chain processes translates into confidence for our clients, guaranteeing the integrity and quality of pharmaceutical products throughout your journey to the patient.

Click the links below to navigate to each article in the series:

1. Introduction
2. Integrating your Cold Chain Management Systems
3. Developing Mature Quality Systems
4. Component Qualification / Installment Qualification (CQ/IQ)
5. Operational Qualification (OQ) for Drug Products
6. Performance Qualification (PQ)

Cold Chain Management Challenges

Competing priorities, changing expectations, cost pressures, sustainability initiatives, and emerging markets – are some of the challenges facing cold chain management professionals every day. Solutions that deliver value in the supply chain and enhance your regulatory reputation are required every day, around the globe. Today, engineers and manufacturers face economic and regulatory pressures, accelerating costs, technology changes, and the need to constantly adapt their business models. The advent of more widely distributed supply chains and other influences demand greater investment in tools, expertise, and, most importantly, human capital.

Investment in these mediums is needed to rise above some of the toughest challenges:

• Appropriate expertise and techniques to assess, control, and communicate risk as part of an ongoing management review process.
• A lifecycle approach to process validation including design, qualification, and verification.
• Better integration of product formulation, controlled environment logistics, and packaging design.
• Innovative, forward-looking quality controls, corrective and preventive actions (CAPAs) strategies, and root cause analyses for once straightforward, highly complex processes today.
• The application of technology to achieve greater gains in all areas, including compliance, quality, and safety.

As the pharmaceutical and biologic industries become global, more API (Active Pharmaceutical Ingredient), Drug Substance (DS), and drug products are being manufactured in one region and transported/imported/exported to other regions around the globe. As a result, supply chain safety and validation are becoming much more critical. Third-party logistics (3PL) partners are increasingly involved in product handling, storage, and distribution. This includes contract manufacturers, repackaging companies, wholesalers, distributors, hospitals, mail delivery and distribution companies, retail pharmacies, logistics companies, freight companies, etc. Other areas that should be included are warehouses, intermediate/temporary storage and transportation areas, operation vehicles, transportation cabins, containers, trucks/automobiles/emergency vehicles, rail cars, ships, etc.

All links along the pharmaceutical supply chain must ensure that product handling, storage, transportation, and distribution are performed appropriately for shock and vibration, temperature, relative humidity, light, oxygen, and other relevant environmental conditions.

Adequate control and monitoring for these conditions should be established and validated to assure product identity, strength, purity, efficacy, quality, and safety.

Temperature and Relative Humidity-Controlled Transportation Products

Temperature and relative humidity-controlled transportation products require special temperature, relative humidity handling, and equipment usage during storage, transportation, and distribution. These products may be shipped outside their official storage conditions, onlybased on approved stability data or other scientific/technical justification that product quality will not be affected by product manufacturing until arrival at patients.

The US FDA, EMEA, ICH, and a host of other regulatory agencies have issued guidance documents on principles of process validation. However, most do not address transport issues specifically. The requirement to validate all critical-to-quality processes remains. There are new approaches to answer these questions on how transport networks can be validated.

Cold Chain Transportation

Cold chain transportation can be validated just like any other process. Process validation aims to create a robust process that consistently produces product with minimal variation. The same goal is set for your distribution processes. By applying good validation principles to your distribution processes, you can validate your transport process. This approach requires qualified packaging and equipment (e.g., over-the-road trucks, active refrigeration units, etc.) and a new approach to process definition for your cold chain transportation network.

In the next article of the series, we will discuss where it all begins – integrating your cold chain management system. You’ll learn about the seven components that work together for a compliant cold chain management system.

How Modality Solutions Can Help:

The pharmaceutical cold chain network is complex, but Modality Solutions makes it easy to simplify and streamline your cold chain. Working as a professional in the cold chain network means facing daily challenges. Just because the pharmaceutical cold chain network is complex doesn’t mean that your management system must be. Let our focused pharmaceutical cold chain engineering firm deliver results with our advanced technology and world-class engineers.

Here’s what you can expect:

• Confidence in your cold chain. Guaranteed.
• Every engagement is led by a principal.
• You can reach out anytime, anywhere, for anything,
• We solve real problems. Your cold chain will be approved.
• You will become cold chain experts.

 

Contact Modality Solutions