Manufacturers in the life sciences industry are under strict supervision by various regulators and governing bodies to ensure the drugs and medicines they produce are safe and effective for the end consumer.
To ensure that manufacturers abide by necessary regulations and their products meet the proper health and safety standards, businesses are required to document every aspect of their operations including the materials used, the personnel involved in production, and the processes that the product went through.
For example, manufacturers under the jurisdiction of the U.S. Food and Drug Administration (FDA) are required to create documentation for each drug formulation and batch they produce.
This documentation allows both internal quality management teams as well as external regulators to ensure that production processes were carried out in accordance with the manufacturer’s plan.
One of the crucial documents that guide pharmaceutical manufacturers’ efforts is the master batch record.
Historically, master batch records have been documented using pen and paper, but within the past decade, more and more manufacturers have invested in digital solutions to help centralize necessary documentation and streamline their compliance records.
In this post, we’ll review the importance of the master batch record and why more pharmaceutical manufacturers are turning to digital solutions to help improve the way they manage their compliance records.
[Free Resource] Pharma 4.0: The Ultimate Guide to Digital Transformation For Life Sciences Manufacturers →
What is a master batch record?
A master batch record (MBR), also known as a master production record (MPR) is a document that contains the approved ingredients, formulation, and instructions guiding the production of a pharmaceutical product. The document enables manufacturers to follow the necessary regulatory guidelines when manufacturing a product.
Because the master batch record governs the entirety of a pharma product’s manufacturing process, it takes on several other names. It is sometimes referred to as a manufacturing batch record, master manufacturing formula, master production record, or master formula record.
Additionally, the master record comes in handy when pharma companies parcel out production responsibilities to outside parties known as contract and developing manufacturing organizations (CDMOs). These organizations follow the master formula record to ensure that they produce quality products safely, consistently, and in compliance with regulatory standards.
Automate data collection and streamline compliance activities
Tulip's digital records solutions allow you to view all digital logbook records, electronic batch records, and equipment activity in one centralized location.
Difference between a batch record and the master batch record
Pharmaceutical production features another compliance document closely linked to the manufacturing batch record. This is known as the batch record, batch manufacturing record, or batch production record.
The similarity lies in the fact that both documents keep track of the approved ingredients and production techniques used by a pharmaceutical manufacturing and are required by regulators to enforce good manufacturing practices (cGMP).
However, there’s a crucial difference. The batch record is a copy of the master. It guides and records the formulations and techniques on the production line to manufacture a specific batch of products. So, apart from providing guidance, the batch record also offers proof that a particular product batch was manufactured according to the procedures detailed in the master formula record.
In other words, the master batch record is a template that businesses can use when creating an individual batch record during the production of a singular batch.
What is included in a master batch record?
In accordance with 21 CFR Part 211, pharmaceutical manufacturers are required to maintain their master batch records with certain details and information. Some of the items that must be included in the MBR includes:
Product name and identification code
Pharma product characteristics and properties
A Bill of Materials detailing the specific ingredients to be added to that particular product formula. This also includes the various sizes and amounts of said ingredients.
Size of the entire batch
Bill of Process showing production line setup, equipment and tools required to make the product
Work instructions for personnel at each stage of the production line
Expected batch yield
Health and safety information to be observed during the production process
Quality assurance and control procedures and acceptable test benchmarks
Approved packaging and storage
These details help ensure that the entire product lifecycle is documented and accounted for, providing evidence that the drugs produced meet the necessary health and safety standards.
Benefits of digitizing your master batch records
Even today, it’s not uncommon for pharmaceutical manufacturers to use paper-based records for their documentation and compliance.
However, the evolution of manufacturing techniques has led to more complex requirements for pharmaceutical production, necessitating more robust compliance document management.
Additionally, manufacturers now have a wide variety of different solutions to choose from when it comes to digitizing their compliance documentation. Some of the key benefits of going digital include:
Integration with ERP systems: Master batch records contain material and process information pertinent to core manufacturing efforts. Integrating the documents with enterprise resource planning systems allows pharma manufacturers to coordinate and manage materials more effectively.
Reduced human errors: Digital solutions eliminate the need for manual data entry, significantly improving data integrity. This ensures that accurate data is collected and documented across every single step of the production process.
Furthermore, some solutions can leverage the master batch record to provide operators with interactive work instructions, allowing personnel to execute their roles more competently and accurately.
Simplified compliance with ALCOA+ principles: In addition to reducing errors associated with human data entry, digital solutions help ensure that documents are aligned with ALCOA as outlined by the FDA.
Not only does implementing a digital compliance solution ensure the data is accurate, but it also ensures legibility, attribution, consistency, and availability to all necessary stakeholders and regulators.
Accountability: Manufacturing batch record software keeps track of all changes made to the document. Not only does this negate the need for double entries across documents, but it also ensures that edits are attributed to the responsible personnel.
Faster information access and retrieval: Compliance audits are significantly more manageable when officers can access documents quickly. Additionally, production personnel can easily retrieve the master record for reference.
How Tulip can help manage your master batch records
As we’ve outlined, the importance of documentation in pharmaceutical manufacturing can not be overstated.
By implementing a solution like Tulip, businesses are able to streamline their documentation and make regulatory compliance a seamless part of their operations.
If you’re interested in learning more about how Tulip can help you manage your master batch records, reach out to a member of our team today!
Improve quality and streamline compliance with Tulip
See how Tulip can help digitize your master batch records to streamline compliance and increase productivity.