Many pharmaceutical manufacturing companies still rely on paper-based processes to comply with strict pharma safety standards and regulations. Time-consuming, failure-prone manual recording poses significant business risks to pharmaceutical manufacturers, such as longer product release times, inventory loss, or even expensive product recalls.
By digitizing their operational checks and processes, pharmaceutical manufacturers can improve their operational efficiency and accelerate time-to-market of products, mitigate risks of brand damage and facilitate ongoing compliance.
Improve productivity and profitability.
Reduce warehousing costs and enable longer product shelf life.
Reduce compliance costs and improve product quality.
Access all data in seconds, mitigating risks of product recalls.
Identify issues faster and reduce costs to rectify them.
Enable faster decision-making, improving efficiency.
iMonitor’s cloud-based pharmaceutical manufacturing software is a manufacturing execution system based on GMP standards and specifically tailored to the needs of the pharmaceutical industry.
The digital manufacturing system, along with industry 4.0 solutions offers significant time and cost savings, and compliance with Medicines Regulations act 1984, GMP, and ISO 22000.
Eliminate paper processes and manual errors to ensure data integrity, real-time visibility and transparency.
Read our 10 steps to successfully implementing a manufacturing execution system here.
Consider these 5 important points when choosing a pharma manufacturing software.