Mumbai headquartered Sage Software Solutions, an ERP, CRM and HCM, announced the deployment of Sage X3 to cater to the specialized ERP needs of Pharma & Bulk Drug Manufacturers. With the Pharma Manufacturers / distributors constantly under pressure to maintain their competitive inventory stock along with an increasing array of regulatory requirements, it was imperative for manufacturers of such products to adopt a flexible industry-specific functionality in order to not only comply with international regulations from the FDA but also to gain competitive advantage.
Sage X3 supports these organizations by facilitating automated support for mission critical functions. Sage X3 can accommodate millions of SKU’s with multiple attributes giving pharma manufacturers a flexibility to maintain the entire product related information and its substitute. It can also scale up to thousands of users using the system. Sage X3 further differentiates itself by seamless integration to external systems.
Commenting on the Sage X3 capabilities for the Pharma manufacturers, Mr. Jitendra Somani, CEO said “Sage X3 equips pharma & bulk drug manufacturers with a strong operational groundwork & agility necessary to steer ahead of competition. In contemporary times, Indian Pharma companies’ urge to grow global is met by conforming to multiple regulatory standards while staying ahead of competition & maintaining operational costs, these three challenges are simultaneously met by Sage X3’s competent benefits helping organizations gain sustainable holistic advantage.”
Besides optimizing the core organizational functions like manufacturing, distribution, warehousing, CRM & accounting functionality, Sage X3 also offers the process specific functionality necessary for the Pharma Industry. Sage X3 functionality naturally fits into the specific needs of the pharma manufacturers by offering the following process based advantages like:-
Sage X3 uses a pre-defined business rules and processes out of the box that drives the market. Sage X3 has functions like process / batch manufacturing, formulation management, expiry management, inventory classification, weight calculations and potency management. Essential requirements such as lot control, shelf-life and traceability are managed within the system along with integrated quality control processes rigorously enforce inspections to assure item conformance and international regulation from FDA.