Requalification of Friability Testing Apparatus

183 Available online at www.derpharmachemica.com ISSN 0975-413X CODEN (USA): PCHHAX Der Pharma Chemica, 2024, 16(1): 183-191 (http://www.derpharmachemica.com/archive.html) Requalification of Friability Testing Apparatus Chethan TP*, Kavya, Abhishek Singh, Rishu Yadav, Laxmi Yadav, Samruddhi Phansekar, Shailendra Gupta and Shubham Yadav Yadav Department of Pharmaceutical Quality Assurance, Priyadarshini College of Pharmacy, Koratagere, India *Corresponding author: Chethan TP, Department of Pharmaceutical Quality Assurance, Priyadarshini College of Pharmacy, Koratagere, India, E-mail: chet[email protected] Received: 28-December-2023, Manuscript no: DPC-23-123880, Editor assigned: 02-January-2024, PreQC No: DPC-23-123880 (PQ), Reviewed: 16-January-2024, QC No: DPC-23-123880, Revised: 18-January-2024, Manuscript No: DPC-23-123880 (R), Published: 08-February-2024, DOI: 10.4172/0975-413X.16.1.183-191 ABSTRACT Re-qualification as a part of validation is the task performed to identify or check that utilities, equipment and ancillary systems can operate within limits for their intended use. Equipment qualification is a key element in the pharmaceutical quality system. In recent times regulatory agencies are more focusing on qualification of equipment. Re-qualification of the equipment starts from design of the equipment based on the user requirement specification and functional requirement specification. The review article provides information on design qualification which is done to identify whether the proposed design of facilities, system and equipment is suitable for intended purpose, installation qualification which is done to check whether the equipment is built and installed in compliance with design specification, operational qualification in which the process parameters shall be challenged to assure that product meets all requirements and finally performance qualification to demonstrate that the process will produce acceptable product consistently under normal operating conditions. Keywords: Re-qualification; Operational qualification; Design qualification; Installation qualification; Performance qualification INTRODUCTION In the pharmaceutical industry, the concept of qualification plays a pivotal role in ensuring the safety, efficacy and reliability of pharmaceutical products. Qualification encompasses a systematic and rigorous approach to evaluating and verifying the various components, processes and personnel involved in the production and distribution of medications. It serves as a fundamental mechanism for meeting regulatory requirements, adhering to industry best practices and maintaining the highest standards of quality assurance [1-4]. Pharmaceutical qualification is a crucial process in the pharmaceutical industry that ensures equipment, systems and processes meet predefined standards and regulatory requirements. It encompasses various stages, including Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ). The goal is to guarantee the quality, safety and efficacy of pharmaceutical products by verifying that everything involved in their production and testing functions correctly and consistently. This rigorous qualification process helps maintain compliance with regulatory agencies like the FDA and ensures the reliability of pharmaceutical manufacturing. It is the action of providing and documenting that equipment or ancillary systems are properly installed, work correctly and leads to the expected results.  Qualification is a part of validation, but the individual qualification steps alone do not constitute process validation.  Qualification of analytical instrumentation is essential for accurate and precise measurement of analytical data. What is qualification? Qualifications are the criteria which an applicant must meet to be eligible for an opportunity award. Qualifications are used to narrow the field of all applicants to only the most qualified applicants. Types of qualification Qualifications are created from the imported data on the import file, student answered questions on the general or conditional applications and/or apply to opportunity questions (Figure 1). MATERIALS AND METHODS Chethan TP, et al. Der Pharma Chemica, 2024, 16(1): 183-191 Figure 1: Types of qualification. Process qualification: Process qualification is the qualification of manufacturing and production processes to confirm they can operate at a certain standard during sustained commercial manufacturing. Data covering critical process parameters must be recorded and analyzed to ensure critical quality attributes can be guaranteed throughout production. This may include testing equipment at maximum operating capacity to show quantity demands can be met. Once all processes have been qualified the manufacturer should have a complete understanding of the process design and have a framework in place to routinely monitor operations. Only after process qualification has been completed can the manufacturing process begin production for commercial use. Equally important as qualifying processes and equipment is qualifying software and personnel. A well-trained staff and accurate, thorough records helps ensure ongoing protection from process faults and quick recovery from otherwise costly process malfunctions. In many countries qualification measures are also required, especially in the pharmaceutical manufacturing field [5-10]. Process qualification should cover the following aspects of manufacturing:  Facility  Utilities  Equipment  Personnel  End-to-end manufacturing  Control protocols and monitoring software Design qualification: Design Qualification (DQ) is a crucial phase in the design and development process of a product or system, especially in industries like pharmaceuticals, biotechnology and manufacturing. It ensures that the design meets the intended requirements and specifications before moving on to further stages of development. Here's a simplified outline of the steps involved in a typical design qualification process:  Define user requirements: Begin by clearly defining the user or stakeholder requirements. What does the product need to achieve? What are the critical parameters and specifications it must meet?  Develop design specifications: Based on user requirements, create detailed design specifications that outline how the product or system will fulfil those requirements. This includes technical specifications, materials, components and functionality.  Design review: Conduct a comprehensive design review with a cross functional team, including engineers, designers and relevant stakeholders. This step ensures that the design aligns with the user requirements and that any potential issues or risks are identified.  Risk assessment: Perform a risk assessment to identify and evaluate potential risks associated with the design. This could include safety concerns, compliance with regulations and any other relevant factors.  Prototype and testing: Build prototypes or conduct simulations to verify that the design functions as intended. Testing should cover various scenarios and conditions to ensure reliability and performance.  Documentation: Maintain thorough documentation throughout the DQ process. This includes records of design changes, test results, risk assessments and design reviews.  Approval: Seek approval from relevant stakeholders and regulatory authorities, if applicable. This step confirms that the design is qualified to move forward.  Validation: Once DQ is complete, the design can proceed to the validation phase, where it is tested under real world conditions to ensure it meets user requirements.  Continuous monitoring: After implementation, the design continues to be monitored to ensure it performs as expected throughout its lifecycle.  Change control: Implement a robust change control process to manage any modifications or updates to the design post-qualification. Design qualification is a critical step to ensure that a product or system is reliable, safe and meets its intended purpose. It helps minimize risks, ensures compliance with regulations and provides a solid foundation for subsequent phases of development and production. Operational qualification: Operational Qualification (OQ) is a critical phase in the validation process, particularly in regulated industries such as 184 Chethan TP, et al. Der Pharma Chemica, 2024, 16(1): 183-191 pharmaceuticals, biotechnology and manufacturing. OQ ensures that equipment, systems or processes operate effectively and consistently within their specified operational limits. Here's an overview of the operational qualification process:  Establishing test criteria: Define the specific criteria and parameters that need to be tested during the OQ phase. These criteria are typically based on the equipment or system's design specifications, user requirements and regulatory guidelines.  Test protocols: Develop detailed test protocols that outline the procedures for conducting OQ testing. These protocols should include step-by-step instructions, acceptance criteria and the equipment and personnel responsible for performing the tests.  Performance testing: Execute a series of tests to evaluate the equipment or system's performance under various operating conditions. This may include testing different operational modes, running the equipment at maximum and minimum settings and assessing its response to normal and abnormal situations.  Data collection: Collect comprehensive data during the testing process, including measurements, observations and any deviations or issues encountered. It's essential to maintain accurate and detailed records.  Data analysis: Analyze the collected data to determine whether the equipment or system meets the predefined acceptance criteria. Any discrepancies or failures should be thoroughly investigated and documented.  Documentation: Maintain comprehensive records of the OQ testing, including test protocols, test results, data analysis and any corrective actions taken to address identified issues.  Review and approval: Review the OQ documentation and test results with relevant stakeholders, including quality assurance personnel and regulatory authorities if necessary. Seek approval for the successful completion of the OQ phase.  Requalification: Periodic requalification may be required to ensure that the equipment or system continues to operate within specifications. This may be triggered by factors such as equipment maintenance, software updates or changes in operating conditions.  Operational qualification is crucial to ensure that equipment and systems perform consistently and reliably within their specified operational parameters. It provides confidence that the equipment or process is capable of consistently producing the desired results and is a fundamental step in achieving regulatory compliance and product quality in regulated industries. Performance qualification: Performance Qualification (PQ) is a critical phase in the validation process, particularly in regulated industries such as pharmaceuticals, biotechnology and manufacturing. PQ demonstrates that equipment, systems or processes consistently produce results that meet predetermined acceptance criteria and are suitable for their intended use. Here's an overview of the performance qualification process:  Test criteria and acceptance criteria: Define the specific test criteria and acceptance criteria for the equipment, system or process. These criteria should be based on user requirements, design specifications and industry regulations.  Test protocols: Develop detailed test protocols that outline the procedures for conducting PQ testing. These protocols should include step-by-step instructions, acceptance criteria and the equipment and personnel responsible for performing the tests.  Performance testing: Execute a series of tests under actual or simulated operational conditions to verify that the equipment or system consistently meets the predetermined criteria. This involves running the equipment or process for an extended period to assess its performance over time.  Data collection: Collect comprehensive data during the testing process, including measurements, observations and any deviations or issues encountered. It's essential to maintain accurate and detailed records.  Data analysis: Analyze the collected data to determine whether the equipment, system or process consistently meets the predefined acceptance criteria. Any discrepancies or deviations from expected performance should be investigated and documented.  Documentation: Maintain comprehensive records of the PQ testing, including test protocols, test results, data analysis and any corrective actions taken to address identified issues.  Review and approval: Review the PQ documentation and test results with relevant stakeholders, including quality assurance personnel and regulatory authorities if necessary. Seek approval for the successful completion of the PQ phase.  Continuous monitoring and maintenance: After successful PQ, the equipment, system or process should be subject to ongoing monitoring and maintenance to ensure that it continues to perform within specifications. Periodic requalification may also be necessary.  Performance Qualification is a critical step in demonstrating that equipment, systems or processes are capable of consistently producing results that meet quality and regulatory requirements. It provides assurance that the equipment or process is suitable for its intended purpose and is a fundamental component of ensuring product quality and regulatory compliance in regulated industries. Installation qualification: Installation Qualification (IQ) is one of the key steps in the validation process, particularly in regulated industries like pharmaceuticals, biotechnology and manufacturing. IQ ensures that equipment, systems or facilities have been installed correctly and in accordance with their design specifications. Here's an overview of the installation qualification process:  Documentation review: Begin by reviewing documentation related to the equipment or system being installed. This includes design specifications, user requirements and any relevant Standard Operating Procedures (SOPs).  Installation verification: Physically verify that the equipment or system has been installed correctly. This involves confirming that it is in the right location, connected properly and in compliance with design specifications.  Calibration and configuration: Ensure that any instruments or sensors are calibrated and configured according to the manufacturer's recommendations and user requirements.  Utility services: Verify that all necessary utility services (e.g., power, water, gas) are properly connected and functioning as required.  Environmental conditions: Check and document environmental conditions such as temperature, humidity and cleanliness to ensure they meet the specified criteria for the equipment or system.  Safety checks: Confirm that safety features and precautions are in place and operational. This includes emergency stop buttons, safety interlocks and alarms.  Functional testing: Perform basic functional tests to ensure that the equipment or system operates as expected. This may include running diagnostic tests and verifying that all components are functioning correctly.  Documentation and records: Maintain detailed records of the IQ process, including photographs, test results and any deviations or issues encountered.  Review and approval: Once the installation has been successfully qualified, review the IQ documentation and seek approval from relevant stakeholders and regulatory authorities if required. Installation qualification is a critical step to ensure that the equipment or system is set up correctly and is ready for further validation activities, such as Operational Qualification (OQ) and Performance Qualification (PQ). It provides assurance that the infrastructure is in place to support the intended processes and functions within regulated industries, where precision and compliance are paramount. 185 Chethan TP, et al. Der Pharma Chemica, 2024, 16(1): 183-191 Requalification: In accordance with the WHO prequalification procedure, holders of prequalified Finished Pharmaceutical Products (FPPs) should submit a quality review five years after the date of prequalification or will be invited to do so earlier if WHO considers this to be necessary. This procedure forms part of the maintenance of the prequalified FPP and is called “requalification”. The procedure is applicable only to FPPs that have been requalified via the full assessment (multisource generic) route. WHO assesses the data and information submitted in the quality review to verify that the prequalified product continues to meet current norms and standards. It also uses the data and information supplied to assess the consistency of product quality and manufacturing processes over the identified period. Requalification is a process in which a person or entity undergoes evaluation or testing to determine if they still meet certain qualifications or standards. It is often used in various contexts such as professional certifications, employment and regulatory compliance to ensure that individuals or organizations continue to meet the necessary criteria. Requalification may involve examinations, training or other assessments to maintain a specific status or certification. Need of requalification: In the pharmaceutical industry, requalification is essential for several reasons:  Regulatory compliance: Pharmaceutical companies are subject to strict regulatory requirements to ensure the safety and efficacy of their products. Requalification helps maintain compliance with these regulations, such as Good Manufacturing Practices (GMP), which require periodic validation and revalidation of equipment and processes.  Product quality and safety: Ensuring that equipment, facilities and processes remain in a state of control is crucial for maintaining the quality and safety of pharmaceutical products. Requalification helps identify and rectify any deviations or issues that may affect product quality.  Process changes: Pharmaceuticals often undergo process changes or upgrades to improve efficiency or comply with new regulations. Requalification is necessary to verify that these changes do not compromise product quality or safety.  Equipment maintenance: Pharmaceutical equipment must be regularly maintained to ensure accuracy and reliability. Requalification helps confirm that equipment functions correctly and consistently.  Risk management: Requalification serves as a risk management tool by identifying potential sources of contamination, errors or product deviations. Addressing these issues proactively helps minimize the risk of product recalls or adverse events.  Product lifecycle: Over time, pharmaceutical products may remain on the market for many years. Requalification helps ensure that manufacturing processes and product quality remain consistent throughout the product's lifecycle.  Continuous improvement: Requalification provides opportunities for continuous improvement by identifying areas where processes or equipment can be optimized for better performance, cost-efficiency and safety [11,12]. Overall, requalification in the pharmaceutical industry is critical for maintaining product quality, patient safety and regulatory compliance throughout the entire lifecycle of pharmaceutical products and processes. The primary objective of the re-qualification process for the friability tester is:  To ensure the continued accuracy, precision and reliability of the equipment in accordance with regulatory requirement and industrial standards.  To assess and document the performance of the equipment, identifying any deviation from specifications and implementing necessary corrective actions to maintain the integrity of test results (Tables 1-6). Protocol for re-qualification Table 1: Installation verification check list. Sr. No Checks to be performed Acceptance criteria Observation Checked by 1. Check for any scratches on the machine body and drums It shall not have any scratches on machine body and drums 2. Check for electrical connection It shall not observe a loose or damage connection 3. Check for levelling of the platform Air bubble of level indicator should be at centre 4. Check drum properly locked with knob on the shaft Drum should be properly locked with knob on the shaft Table 2: Site inspection checklist Sr. No. Parameter Acceptance criteria Observation Checked by 1. Room temperature 15°C to 30°C 2. Room environmental checks Away from direct sunlight Free from vibration No corrosive gases 3. Table space Width: 15” Length: 18” Height: 20” 4. Point for electrical connection Single phase of 230 V AC 50 Hz 186 RESULTS AND DISCUSSION Chethan TP, et al. Der Pharma Chemica, 2024, 16(1): 183-191 5. Base/table level Levelled sturdy, with no vibration 6. Earthing Shall be provided Table 3: Utility verification checklist Sr. No Parameter Acceptance criteria Observation Checked by 1 Phase voltage Single phase, 220/230 VAC, 50/60 Hz Table 4: Technical specification checklist. Sr. No. Test Acceptance criteria Observation Checked by 1. Speed 25 Revolutions Per Minute (RPM) 2. Count range 01 to 99 revolutions. 3. Type of the drum Electro lab AD drum and abrasion drum. 4. Power supply Single phase, 220/230 V AC, 50/60 Hz 5. Dimension 350 mm (L) × 310 mm × 430 mm (H) 6. Weight 12 Kg. (approx.) 7. No. of drums 01 Nos. 8. No. of discharge trays 01 Nos. Table 5: Drums specification check list. Sr. No. Name Acceptance criteria (As per USP general chapter-1216) Observation Checked by 1 1 Drums One side removable Material Transparent synthetic polymer with polished internal surfaces 187 Chethan TP, et al. Der Pharma Chemica, 2024, 16(1): 183-191 Table 6: Operational verification checklist. Sr. No. Operation Acceptance criteria Observations Checked by 1 Switch ‘ON’ the power switch. The drum shall initialize itself to the loading position. The display shall now show ‘start” 2 Press ‘RESET’ key. The instrument shall initialize and they will stop at the loading position. Performance of instrument Performance of instrument is checked by taking different size or shape of tablets (different size or shape of tablets causes a regular and irregular tumbling). Initially weighed tablets are transferred gently into the drum from the side slit provided on the drums. The TIME mode is set for 4 minutes i.e., 100 rotations. Calculated the friability and result is recorded in following Tables 8-14. % Friability=(Initial weight in gm-final weight in gm)/Initial weight in gm × 100  For regular tumbling, set the instrument at normal position, as there is not any irregular tumbling of tablets.  For irregular tumbling, set the instrument with 10° tilt with the bench top to prevent any irregular tumbling of tablets. Acceptance criteria: Performance of instrument shall be found satisfactory. Table 7: Data protocol for normal position. Product name: No. Time set in minute Initial weight in gm Final weight in gm Friability Acceptance criteria Checked by 1 NMT 1% 2 3 Calculation for normal position: % Friability=(Initial weight in gm-final weight in gm)/Initial weight in gm × 100 Table 8: Data protocol for 10° tilt position. Product name: No. Time set in minute Initial weight in gm Final weight in gm Friability Acceptance criteria Checked by 1. NMT 1% 2. 3. Calculation for 10° tilts position: % Friability=(Initial weight in gm-final weight in gm)/Initial weight in gm × 100 188 Chethan TP, et al. Der Pharma Chemica, 2024, 16(1): 183-191 Re-qualification report Table 9: Installation verification check list. Sr. No Checks to be performed Acceptance criteria Observation 1. Check for any scratches on the machine body and drums It shall not have any scratches on machine body and drums No scratches found 2. Check for electrical connection It shall not observe a loose or damage connection No loose or damage connection found 3. Check for levelling of the platform Air bubble of level indicator should be at centre In the level on the platform 4. Check drum properly locked with knob on the shaft Drum should be properly locked with knob on the shaft Properly locked with knob on the shaft Table 10: Utility verification checklist. Sr. No Parameter Acceptance criteria Observation 1 Phase voltage Single phase, 220/230 VAC, 50/60 Hz. Pass Table 11: Technical specification checklist. Sr. No. Test Acceptance criteria Observation 1. Speed 25 Revolutions Per Minute (RPM) Pass 2. Count range 01 to 99 revolutions. Pass 3. Type of the drum Electro lab AD drum and abrasion drum. Pass 4. Power supply Single Phase, 220/230 V AC, 50/60 Hz Pass 5. Dimension 350 mm (L) × 310mm × 430 mm (H) Pass 6. Weight 12 Kg. (approx.) Pass 7. No. of drums 01 Nos. Pass 8. No. of discharge trays 01 Nos. Pass 189 Chethan TP, et al. Der Pharma Chemica, 2024, 16(1): 183-191 Table 12: Drums specification check list. Sr. No. Name Acceptance criteria (As per USP general chapter-1216) Observation 1 Drums One side removable Single side Material Transparent synthetic polymer with polished internal surfaces Pass Report: Drum Specification check point was verified; observations were noted above. Table 13: Operational verification checklist. Sr. No. Operation Acceptance criteria Observations 1. Switch ‘ON’ the power switch. The drum shall initialize itself to the loading position. The display shall now show ‘Start” Pass 2. Press ‘RESET’ key. The instrument shall initialize and they will stop at the loading position. Pass Report: Operational verification check point was verified; observations were noted above. Performance of instrument Acceptance criteria: Performance of instrument shall be found satisfactory. Table 14: Data for normal position. Product Name DOLO 650 Sr. No. Time Initial weight in gm Final weight in gm Friability Acceptance criteria Checked Set in minute by 1. 04 Min 6.845 6.842 0.04% NMT 1% 2. 04 Min 6.831 6.831 0.02% 3. 04 Min 6.83 6.81 0.20% Calculation for normal position: % Friability=(Initial weight in gm-final weight in gm)/Initial weight in gm × 100  1st trail=(6.845-6.842)/6.845 *100=0.04%  2nd trail=(6.831-6.829)/6.831*100=0.02%  3rd trail=(6.830-6.810)/6.830 *100=0.2% Report: All 3 trails of tablets (DOLO 650) are within the acceptance criteria. Hence the tablets pass the friability test as per USP. 190 Chethan TP, et al. Der Pharma Chemica, 2024, 16(1): 183-191 Requalification The requalification has been carried for the friability tester by using two different shaped tablets of same dose. The performance of the equipment tested. Results were found satisfactory and with the acceptance criteria [13-15]. In two variations performance qualification carried out i.e.,  At normal position  At 10° tilt position CONCLUSION The samples (marketed tablets) of different shapes taken for the performance qualification, the friability tester passed the all the parameters of Installation, operational and performance qualification. After reviewing the results of all parameters, the parameters of installation, operational and performance qualification, following points are concluded.  The friability tester passed the all the parameters of Installation and operational qualification without any failure.  Coming to performance qualification, at normal position the equipment taken for 3 trails, all the trails are within the limit and equipment as per the USP.  At 10° tilt position the equipment taken for 3 trails, all the trails are within the limit and equipment as per the USP.  From the above results we can conclude that the equipment able to achieve continued accuracy, precision and reliability of the equipment in accordance with regulatory requirement and industrial standards. ACKNOWLEDGEMENT The authors are grateful to the Blatter herbarium, St. Xavier’s college, Mumbai for helping us with the authentication of the plant samples. We are also thankful to the entire staff at Anchrome enterprise Pvt. Ltd. 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