Lab equipment validation is essential for the compliance of regulatory bodies and ensuring that the instruments meet the required standards. It is also important to ensure that the equipment meets the required quality for a specific lab process. When validating lab equipment, ensure that you follow the manufacturer’s specifications. The validation results must be consistent with various equipment parameters. However, guaranteeing each critical component of the equipment is suitable takes more time. When working in highly regulated sectors such as pharmacy, medical, and food industries, the validation process must follow FDA stringent measures.
Due to the complex process of lab equipment validation, lab users must devise measures to improve efficiency. When you streamline the validation process, getting faster results becomes easier.
Here are Ways to Get Faster Instruments Validation Results
Deciding The Type of Equipment to Validate and Their Schedule
The best way of getting validation results is to make a validation schedule for each instrument. It is easier to prepare for the validation of various devices using a clear program. You can achieve this by categorizing your equipment from simple instruments to more complicated ones. In addition, you can create a specific time for validating instruments in various classes. Such classes may include instruments such as analytical equipment, chambers, autoclaves, and spectrophotometers. If you want to simplify your validation process, perform the tasks at specific intervals or events. You can decide to perform lab equipment validation during installation, maintenance, or moving to a new location. Another instance of lab equipment validation is when a new protocol is introduced.
Outsourcing Lab Equipment Validation Process
If you want faster validation results, contact a professional third-party company. These companies have the necessary resources for various validation processes. Performing in-house validation can be tedious and time-consuming. You might also incur additional costs for validation equipment. However, if you want to make your in-house validation faster, draft validation templates to be used by your staff. The templates will consist of the procedures and the components to be validated at a particular time. For consistency and accuracy, draft clear validation documentation. Your documentation needs to have organized protocols for faster results. Moreover, you can invest in validation software to track your process, automate schedules and provide paperless results.
Introduce an Integrated System
It is important to introduce an analytical technology for your validation process. An integrated system will save your time and reduce various validation risks. Introducing a management system will allow you to eliminate paper records that are time-consuming and have transcription errors. A management system is useful when tracking various instruments, assets, and validation schedules. With the growth of technology, you can automatically compute and network your validation data. In addition, software solutions are reliable, accurate, and sustainable.
A paperless system is seamless, accurate, and efficient. In addition, various regulatory bodies, such as the FDA, requires that you set up a paperless system. Managing validation records is difficult and full of errors. Furthermore, retrieving past validation records is tedious and may lead to data loss. An automated system is faster and increases the number of validation tasks daily. Moreover, a system rids you of enormous junk papers in your office.
Integrate Your Validation Processes
Every system needs integrity and simplicity. You can achieve this by making various backups of your electronic records. An integrated system is also important when extracting previous validation records from your database. Unlike a manual form, an electronic system is searchable, saving your instrument validation time. For faster decision-making, you can integrate your validation records into software for smooth data transfer.
In addition, if you operate several laboratories, you can receive validation reports from a centralized electronic system. The system simplifies your management aspects and ensures that your processes are on track. To streamline the validation workflow, ensure that you train your staff using various analytical instruments. However, consider a full data management software to consolidate every aspect of your instrument validation. The software is important when sharing validation reports outside sources and improving the integrity of your work. Furthermore, the software will also provide validation data accessibility to all your staff. The process will boost your lab productivity and foster collaboration with various stakeholders.
With integrated software, you can use barcodes for a simpler interpretation of data. Labeling instrument components allows faster validation than relying on manual records. The result is a fully functional validation system.
Adhere to Regulatory Requirements
Lab equipment validation requires compliance with various regulatory bodies. Regulatory requirements are always updated for integrity purposes. It is important that you follow these regulatory updates to make your validation faster. Lab owners who fail to follow these requirements are normally fined and ordered to repeat the process. In recent times, the FDA has introduced various electronic validation protocols. Using these protocols allows you to easily manage, analyze and generate validation certificates from electronic data. These measures provide efficiency and save time, making your general validation results faster.
Full Integration of Lab Process
Integrating all your lab process is necessary. However, you should ensure that various processes work seamlessly and simultaneously without bottlenecks. An efficient lab has different software that works harmoniously without interference. These processes improve your productivity in aspects such as lab equipment validation. Furthermore, you can integrate your software with a third-party solution for easier communication. Enabling integration with a third-party solution eliminates the need to exchange validation data using paperwork.
Moreover, a fully integrated lab is valuable for automatic analysis, searchable databases, and compliance with various stakeholders.
Lab equipment validation protocols require accuracy and integrity. Your lab operations must be flexible and efficient if you want faster results. However, you may have several challenges validating your instruments in time. You can contact a specialized third-party validation company for accurate and speedier results. Biotechnical Services, Inc. has enough premier resources for every type of lab equipment validation.