
Constant innovation
In a global economy, where new players continue to enter the market, companies face increasing pressure to launch groundbreaking products.
Free up more time for research and development with automated processes that simplify your work.
Cost pressure
Demand for medicine is increasing globally, while budgets are shrinking. In addition, the pharmaceutical industry spends significant amounts on research.
Our ERP solution helps you act decisively and strategically to remain cost-efficient in the future.
Laws and regulations
Laws and regulations are becoming increasingly complex, and GxP and FDA requirements dominate the working day. The same applies to MDR and UDI.
Our ERP solution supports your work in complying with these standards.
Validation
NORRIQ has delivered ERP projects where, together with the customer, we have ensured that logistics and financial processes are separated from the validation obligation.
In these cases, we make sure that the solution helps and supports the business, and does not need to be validated. We also offer a solution where the ERP system must be validated.
Quality standards
As quality requirements, controls and safety measures increase, companies also face challenges in the form of supplier assessments and regulations.
Our ERP solution for pharma companies enables reliable and continuous quality inspection.
Resource shortage
Access to raw materials is limited, and availability is at times severely restricted. Smooth production planning is necessary to ensure uninterrupted production.
Our ERP solution for pharma process production supports that planning.
GAMP 5 compliance
Traceability
Lot/batch
Quality assurance
Shop floor
Logistics
Capacity management
Tank/silo management
Pre- and post-calculation
Recipe management
Web service/integration/API
PIM product data management
B2B webshop
BI overview and reporting
Documentation and validation
Product lifecycle
Certifications
Expiry date
Label management
Warehouse Management
Everything from quality control to R&D and warehouse management, through to optimised, scanner-supported logistics processes.
With YAVEON ProBatch, you can extend your Business Central capabilities, making everyday work within pharma and MedTech easier, efficient, safe and, of course, validated.
Manage expiry dates, trace goods and forecast production needs.
The requirements for traceability and quality continue to increase, not least because of the risk of a recall. With NORRIQ’s solution, you comply with the specifications of GAMP 5 and meet the requirements for implementing a validated ERP system.
Traceability must be complete: all parts of the supply chain must be covered. Transparency is the key word. It is created through registrations of, for example, quality measurements, shelf life, storage and transport.
With NORRIQ’s solution, you create coherence between:
planning
quality assurance
production and documentation
registration of laboratory quality measurements
traceability
shelf-life management
shop floor control, integrated with payroll
NORRIQ’s solution streamlines and automates purchasing and logistics for pharma producers, so that you always have the right quantities of raw materials in stock and have overview and control over shelf life and lot/batch.
Predictability and pre-calculations are important parameters when ensuring efficient and precise production planning.
With an efficient system for managing demand forecasts, the right decisions can be made in relation to:
purchasing
planning
production
distribution
With a BI solution from NORRIQ, which measures the right KPIs and provides precise analyses for post-calculation, there is great transparency in planning and production processes.
Create lasting customer relationships. Close deals. Grow the business.
If you work with wholesale, your solution can be integrated with a PIM system, warehouse management module and webshop, so that the entire value chain runs smoothly with as few manual workflows as possible.
With NORRIQ’s solution, it is easy to:
optimise sales and marketing processes
manage commission
receive EDI orders via your website
integrate and use the solution together with your e-commerce platform
The solution can also support customer relationships with:
a strong B2B webshop or sales portal
Manage contribution margin per product. Meet customers’ EDI requirements. Analyse where value is created and strengthen the decision-making process.
With NORRIQ’s solution, you can:
budget and design forecasts
collect and manage contracts for customer and supplier agreements
comply with the many requirements within GMP/MDR, for example in relation to FDA
The solution can be integrated with Business Intelligence, enabling you to:
analyse data from many sources
view supplier performance
identify optimisation potential in your own processes and profitability, and much more
Together with a PIM solution, Product Information Management, processes around the management of product information are supported, from production and purchasing to sales and marketing on the web.
This support also applies to information management to and from data suppliers, between production and sales units, and to your own and your customers’ e-commerce solutions. Management of assortments and pre-calculations can also be supported by a PIM solution.
Together with a warehouse management solution, processes are supported using modern scanning technology for goods receipt, put-away, picking for production and optimisation of dispatch logistics.
At the same time, the entire process around batch/lot, shelf life and quality is supported.
Optimise inventory value and warehouse processes with tools for:
label management
traceability
barcodes
goods receipt
pick & pack
When choosing an ERP system for the life sciences sector, you must ensure that it supports compliance with the sector’s regulatory requirements, such as GMP and ISO 13485. It is also important to choose a system that can be validated and integrated with existing processes to ensure quality and traceability in production.
ERP systems for regulated industries help companies meet requirements from authorities such as the FDA and the EU. This includes features for document management, batch tracking and validation of processes in accordance with 21 CFR Part 11. The system must also be flexible enough to handle regulatory changes and ensure continuous compliance.
GMP ensures that products are manufactured and controlled according to quality standards. A GMP-compatible ERP system automates and documents production processes, making it easier to comply with quality requirements, reduce errors and maintain traceability. This is crucial to ensure patient safety and comply with regulatory requirements.