Dynamics 365 pharmaceutical manufacturing software: From master batch record to QA sign-off, in one module.
Run pharmaceutical manufacturing from master batch record to QA sign-off, with formula management, SOPs, deviations, CAPA and complaint handling in the same Dynamics 365 module.
- Master and electronic batch records
- Deviations, CAPA and complaints
- Formulas and BOMs
- Runs on
- Dynamics 365 Finance and Supply Chain Management
- Built for
- Pharmaceutical
- Key records
- Master and electronic batch records · Deviations, CAPA and complaints · Formulas and BOMs
Is this you?
Production, quality and compliance run on separate systems.
Handoffs between teams happen by email.
Release depends on chasing paperwork.
From master batch record to QA sign-off, in one module.
From event to evidence
- 01Master batch records
Define the master batch record once, then generate an electronic batch record from it for every production order.
- 02Electronic batch records
Follow every batch from orders created to reported as finished, with approval to start, post-production approval and QA sign-off.
- 03Quality in the flow
Deviation management, CAPA and complaints management, each with its own workspace and linked to the batch.
- 04Formulas and quality
Bills of materials, formulas, SOPs and Dynamics 365 quality management in the same module.
iPM inside Dynamics 365
6 screens your team would actually use.
Standard Dynamics 365 layout, with iPM adding the records, workflow and sign-off.
One workspace for batches, deviations, CAPA and complaints, with what needs attention first
Illustrative screens with demo data · Standard Dynamics 365 layout
QUALITY PERFORMANCE
What to measure.
Illustrative improvement targets. Actual results will vary
Questions, answered
Questions about iPM.
Real questions from buying committees, answered plainly.
Will this work with the Dynamics 365 we already run?
Yes. Our products are built for Dynamics 365 Finance and Supply Chain Management, so quality, batch and SOP records sit next to finance, production and inventory. iQM is also available for Dynamics 365 Business Central.
How do you handle validation?
Validation plans, scripts and evidence are part of every regulated engagement, assembled as we build, not after.
Who supports us after go-live?
The same team. Application management, release testing and continuous improvement.
What is rapid implementation?
A fixed scope, team and timeline, with processes preconfigured for your industry and XcelPros products included where they fit.
Do we have to license all five products?
No. Each product is licensed separately. Most teams start with one and add more.
Is this only for pharma?
No. We work with pharmaceutical, chemical, food & beverage, manufacturing and distribution companies.
Are you a Microsoft partner?
Yes. XcelPros is a Microsoft Dynamics 365 partner, and our products run inside Dynamics 365.
Can we run iQM on Business Central?
Yes. iQM is available for Dynamics 365 Business Central as well as Finance and Supply Chain Management. Ask us which fits your size and requirements.
What does iPM include?
Master and electronic batch records, SOPs, deviation management, CAPA, complaints, formulas and quality management, in one module.
How does iPM relate to iQM, iBR and iSM?
iPM brings them together for pharmaceutical manufacturers. The individual products suit teams that need one area.
Does it work with our existing Dynamics 365 setup?
Yes. iPM is built for Dynamics 365 and uses your existing items, sites and users.
Get started
Tell us what you need.
Dynamics 365 consulting, full or Rapid implementation, and support from one team.