ERP for Pharmaceutical Industry

Pharmaceutical ERP

The pharmaceutical manufacturing industry is a highly regulated industry with a lot of radical changes happening in the recent past. To keep up with the constantly changing market trends, changes in the healthcare sector, frightening global competition, Pharmaceutical companies need to adapt faster and, at the same time ensure that the changes are complied and followed. 

This is best done by the use of technology and systems. There are some specific ERP solution for pharmaceutical industry which can help Pharma companies embrace these changes. 

Designed for Batch Manufacturing

The ERP system should be designed for the batch manufacturing and pharmaceutical industry and not “customised” for it as there are a lot of inherent structural needs of a batch manufacturing that cannot be addressed by a customisation , add-on or retrofitting an existing ERP solution. ERP for pharma companies are most suitable.

Quality Control & Traceability 

Quality Control is the most important point for successful and effective ERP system. QC and QA in Pharmaceutical ERP cannot be a separate “module” but tightly integrated with all processes of the Supply chain and Manufacturing. In the Pharma industry the QC and QA should be omnipresent across the entire ERP Pharmaceutical process.

Regulatory Compliance

Almost all of the facts that have to be recorded and accounted for in regulatory compliance can be maintained in ERP system and its database(s). Financial accounting transactions are obvious, but ERP extends the capabilities to traceability of products through their manufacturing and distribution cycle. 

The ERP software should be able to pass any system validation and for organisation catering to the US FDA , it should have the capabilities to clear a USFDA 21 CFR part 11 validation. 

Audit Trails 

When and how was the data recorded, who approved it and when, did anyone change it. Granular audit trails are mandatory for any system used in a highly regulated industry like pharma, healthcare and food.

Data security

Data is an important asset to any organization. The pharma manufacturing ERP software boasts an array of security features such as access controls, data encryption, audit trails, electronic signatures and passwords, among others.

Production as per cGMP norms

Your ERP solution should help you to achieve a compliance by aiding your manufacturing process and ensuring the record maintenance are as per defined cGMP guidelines.

Online availability of data

Online availability of consolidated data is a big advantage when it comes to planning the sales strategy and getting instant MIS for other business decisions. This is relevant to any company using an ERP.

To know more visit: www.proteustech.in

 

ERP for Pharmaceutical Industry

Pharmaceutical ERP

The pharmaceutical manufacturing industry is a highly regulated industry with a lot of radical changes happening in the recent past. To keep up with the constantly changing market trends, changes in the healthcare sector, frightening global competition, Pharmaceutical companies need to adapt faster and, at the same time ensure that the changes are complied and followed. 

This is best done by the use of technology and systems. There are some specific ERP solution for pharmaceutical industry which can help Pharma companies embrace these changes

Designed for Batch Manufacturing

This is best done by the use of technology and systems. There are some specific ERP solution for pharmaceutical industry which can help Pharma companies embrace these changes.

Quality Control & Traceability 

Quality Control is the most important point for successful and effective ERP system. QC and QA in Pharmaceutical ERP cannot be a separate “module” but tightly integrated with all processes of the Supply chain and Manufacturing. In the Pharma industry the QC and QA should be omnipresent across the entire ERP Pharmaceutical process.

Regulatory Compliance

 Almost all of the facts that have to be recorded and accounted for in regulatory compliance can be maintained in ERP system and its database(s). Financial accounting transactions are obvious, but ERP extends the capabilities to traceability of products through their manufacturing and distribution cycle. 

The ERP software should be able to pass an system validation and for organisation catering to the US FDA , it should have the capabilities to clear a USFDA 21 CFR part 11 validation. 

Audit Trails 

When and how was the data recorded, who approved it and when, did anyone change it. Granular audit trails are mandatory for any system used in a highly regulated industry like healthcare and food.

Data security

 Data is an important asset to any organization. The pharma manufacturing ERP software boasts an array of security features such as access controls, data encryption, audit trails, electronic signatures and passwords, among others.

Production as per cGMP norms

Your ERP solution should help you to achieve a compliance by aiding your manufacturing process and ensuring the record maintenance are as per defined cGMP guidelines.

Online availability of data

Online availability of consolidated data is a big advantage when it comes to planning the sales strategy and getting instant MIS for other business decisions. This is relevant to any company using an ERP.

To know more visit: www.proteustech.in

 

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