CONQUER COMPLIANCE, CONTROL COSTS
with an MIS/ERP Tailored to Pharma
FIVE WAYS AN MIS/ERP ACHIEVES REGULATORY COMPLIANCE
Both brand owners and pharmaceutical manufacturers have been much in national news this last year. Packaging, label, and flexographic packaging companies are likely closely examining practices, procedures, training—and the way data is collected and reported as a result.
The spotlight brightly shines on pharma after incidents that focused on non-compliance. In an article published by Reuters, the FDA cited Eli Lilly’s Branchburg, New Jersey, facility on two counts of inadequate “control of computer systems.” Those two findings included deleted data on the company’s manufacturing processes and failed quality control over audit paper trails. Emergent, too, faced violations for inadequate controls for computer and records systems, according to a PharmaExec article.
Compliance issues are critical…
Can those involved in regulatory environments – pharma, food & beverage, cosmetics, and now, cannabis–avoid problems like those described above? Can stake holders choose management systems that not only ensure quality control and compliance, but also provide efficient solutions for business and manufacturing management?
An MIS/ERP for those in packaging, label and flexographic businesses can be that all-in-one answer to ensure companies which operate in a regulated environment won’t encounter problems for the brand owner after hitting the market. In today’s regulatory driven market, technology, like the automation in an MIS/ERP, AI, MES and IIoT can assist manufacturers not just on the plant floor, but also in quality control, data reporting and accuracy.
Let’s examine five ways an MIS/ERP achieves regulatory compliance for packaging and label, and flexographic manufacturers.
A lack of data accuracy can be a heavy weight a business trudges around and it slows down every aspect of your production. What data are collected? How often? Where is it stored? Is it seamlessly integrated into your quality management system? Is it reliable?
Consider the ways to capture data, such as smart sensors (MES) on machines and Industrial Internet of Things (IIoT), that will record information in real time and funnel the data back to one central database of an MIS/ERP where all job information and updates are stored.
Re-makes, downtime, labor costs—lowered. Just by collecting accurate data.
The digital transformation is fundamentally changing the way industries are doing business, and it has unique implications for regulated industries like pharmaceuticals.
In the past, paper had been the gold standard when it came to appeasing regulators. It provided the ‘evidence’ of compliance. Now that we are in the 2020s, pharmaceutical companies have options to paper that are secure as well as likely more accurate. Paper data collection is cumbersome and a time consuming process demanding additional costs of a quality control staff. A digitized audit trail for anyone who is investigating the product life cycle from beginning to end is readily available for auditors and streamlines an audit.
This is one way comprehensive MIS/ERP solutions offer peace of mind to pharmaceutical manufacturers and brand owners.
Another key to achieving regulatory compliance is to remove barriers to connectivity: Uniting data, machines, and processes with a common platform. With all your quality and compliance data in one place, manufacturing and business processes can move faster and be more responsive.
Often in regulated industries, business processes are siloed from manufacturing, and manufacturing siloed from quality control and QMS systems. Even within a production workflow, elements of the workflow itself have disparate apps and software that are unconnected. Pieces and parts that hold crucial data necessary for compliance which need lots of manual aid to connect them. Having an integrated platform saves costs by eliminating manual processes. A bi-directional communication between the shop floor and the management system creates connectivity and accurate data collection.
An MIS can also connect to third-party quality control software, and any other app or software that then creates a streamlined, connected system.
FDA has stringent “Track and Trace” validation requirements. The Drug Supply Chain and Security Act (DSCSA), suggests that digital record keeping tools which integrate shop floor data collection, such as machine sensors, are very important to the modern pharma manufacturing. Having all data in one data repository.
Because all records must be traceable and easily retrievable, they must be managed and controlled. An MIS/ERP will enable a pharmaceutical manufacturer to offer smart data management solutions to intelligently track & trace to provide product tracing documentation.
Between now and 2022, the U.S. Food and Drug Administration’s (FDA) will be increasingly able to travel and conduct onsite inspections.
CAPAs. Batch records. Electronic records. Audit trails. Regulated products generate an endless stream of information. In the FDA’s point of view, if it is not documented, it did not happen. Proper documentation is imperative. An MIS/ERP configured for the all the appropriate reporting can generate the records showing that all manufactured products meet regulatory specifications.
Between now and 2022, the U.S. Food and Drug Administration’s (FDA) will be increasingly able to travel and conduct onsite inspections. While portions of audits and inspections might remain virtual, it’s important for pharmaceutical manufacturers to be prepared to meet this regulatory upshift. Especially in light of high profile companies who were found non-compliant. By automating critical processes like data collection, data traceability, data management and quality control, a pharma manufacturer can stay ahead of audits and be worry-free.
Case Study in Compliance & Cost Control: MTC and HiFlow MIS
MTC is headquartered Vienna, Austria with manufacturing based in Pruszków, Poland. It supplies Poland and exports to over 25 countries including Europe, Scandinavia, as well as the US. The factory in Pruszków employs a staff of 85. MTC delivers high-quality packaging work for pharmaceutical brands, and also provides laminates and specialized foils for cosmetic packaging.
“We are family-owned company with a modern equipped production site with quality certificates implemented—BRC IoP, HCCP, and GMP,” says Lukasz Szczepanski, CFO, MTC Poland. They also meet ISO standards – ISO9001, ISO15378, ISO14001, as well as the stringent EU standards for pharma.
MTC choose HiFlow because of the quality control and compliance features it offered and that it was configurable to exactly what the pharma manufacturer needed. Every single batch of raw material can be tested and approved. If a given batch of raw material does not meet the standards, it can be sent to the complaint warehouse or for destruction. The warehouse employee receives the appropriate disposition in the warehouse module and on the barcode reader with the operating system.
An MIS/ERP can be an invaluable tool to assist pharma, food & beverage, cosmetics, automotive and cannabis companies deal with the evolving regulatory environment. Choose a Smart Factory solution, like HiFlow, today!