Evaluating an ERP for Pharmaceutical Industry

If you are looking for an ERP for pharmaceutical companies then

be sure to get answers to the following questions :

  • Does it manage potency / assay based recipe and calculate the material required?
  • Can you map your manufacturing process validation?
  • Can it track retest dates?
  • Does it track recalibration of your equipment and makes them unavailable for measurement and recording?
  • Does it help you to dispense the right batch of the product for the specified quantity and directly integrated with the weight scales?
  • Does it have print control for controlled documents?
  • Can it integrate with your manufacturing equipment?
  • Is it eBMR capable?
  • How does it help in revalidating a process to avoid human errors?
  • Has it been validated under 21CFR part II or any other system validation for manufacturing?
  • Is the QA, QC process an integral part of the manufacturing, inventory, purchase and logistics module to ensure that QC can be triggered at any point in the supply chain?

These challenges are efficiently addressed in Vision ERP which not only provides better control over the business processes, but also helps manufacturing products as per cGMP guidelines. Hence, the product is one of the most suitable ERP for pharma companies.

Evaluating an ERP for Pharmaceutical Industry

 

If you are looking for an ERP for pharmaceutical companies then be sure to get answers to the following questions :

  • Does it manage potency / assay based recipe and calculate the material required?
  • Can you map your manufacturing process validation?
  • Can it track retest dates?
  • Does it track recalibration of your equipment and makes them unavailable for measurement and recording?
  • Does it help you to dispense the right batch of the product for the specified quantity and directly integrated with the weight scales?
  • Does it have print control for controlled documents?
  • Can it integrate with your manufacturing equipment?
  • Is it eBMR capable?
  • How does it help in revalidating a process to avoid human errors?
  • Has it been validated under 21CFR part II or any other system validation for manufacturing?
  • Is the QA, QC process an integral part of the manufacturing, inventory, purchase and logistics module to ensure that QC can be triggered at any point in the supply chain?

These challenges are efficiently addressed in Vision ERP which not only provides better control over the business processes, but also helps manufacturing products as per cGMP guidelines. Hence, the product is one of the most suitable ERP for pharma companies.

 

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