

Pharma and Process Manufacturing Add-On

Process manufacturing can be an extremely complex process involving various unit operations, yield calculations and stringent quality control norms. From the shifting quality of the ingredients, to the changing environment of the market, being able to make changes ‘on-the- fly’ are paramount. Quality of raw materials, their shelf-life and the impact on entire supply chain process itself make the needs of process manufacturers very challenging. Thus having the right software in place to help manage the entire supply chain & production planning is essential.
RPM Process and Pharma Manufacturing Add-on will help you run your business seamlessly by eliminating the challenges that industries like Chemicals, Pharmaceutical, Paints & Coatings, Speciality Chemicals, Cosmetics and Personal Care products. Our add-on offers a complete solution designed to meet the complexities and ever-changing needs of formula and recipe based “Loan & License” manufacturing. It can handle all your manufacturing, finance, quality and compliance and distribution needs and generate business analytics across all facets of your enterprise including key business processes.
Add-on Functionalities

Add-on Functionalities

Key Functionalities

Batch Production
Create and schedule the optimal number of batch jobs required for a product formula and its multiple packaging configurations, based upon the aggregate demand for the given product.
Costing
Roll up existing and theoretical product costs, as well as fixed, tiered and scalable costs to formulas, intermediates and finished goods during product development.


Quality
From vendor inspection plans to formula and finished good QC testing, establish a comprehensive QA program that ensures the delivery of quality products to your customers.
Compliance
Keep compliant with industry specific and 21 CFR Part 11 FDA regulations, in terms of labeling, lot traceability reports, transactional audit reports and shipping documentation.
Quality
From vendor inspection plans to formula and finished good QC testing, establish a comprehensive QA program that ensures the delivery of quality products to your customers.
Compliance
Keep compliant with industry specific and 21 CFR Part 11 FDA regulations, in terms of labeling, lot traceability reports, transactional audit reports and shipping documentation.
Inventory
Manage inventory based upon quality status, units of measure, expiration date, lot number, strength, license, serial number and location to ensure the right inventory is available for manufacturing and distribution activities.
Maintenance
Establish a preventive maintenance program to avoid unnecessary equipment failures and keep your plant running smoothly.

