O2 Pharmacetuical ERP Software Assists in Documenting Quality Control, Regulatory Requirements & cGMP

In a recent article from PharmaManufacturing.com, they noted that in early results of a survey that "cGMP Compliance is the pharmaceutical industries top manufacturing goal."  As pharmaceutical manufacturing operations increase in complexity due to regulations or processes, finding a way to monitor and track all aspects of operations in a central location becomes important.

O2 Pharmaceutical ERP software assists pharmaceutical and life sciences manufacturers with tracking and tracing quality and regulatory requirements, as well as monitoring cGMP.  This includes:

• CFR 21 Part 11 compliance
• formula security/management
• restricted lot hold
• enhanced implementation documentation 
• cradle-to-grave lot tracking

In order for pharmaceutical manufacturers to remain profitable while managing these key challenge areas, the pharmaceutical manufacturing software also provides:

• inventory forecasting
• inventory requirement planning
• multiple unit of measure calculations
• certificate of analysis (C of A)
• capacity resource scheduling

Finally, an area of concern for pharmaceutical manufacturers is risk and recall situations.  Pharmacuetical manufacturing ERP software, such as O2 Pharmaceutical ERP offers:

• cradle-to-grave lot tracking
• strong auditing and security features
• validation

While the pharmaceutical and life sciences manufacturing industry is extremely competitive and full of critical regulations, there are ERP software programs built specifically for the industry.  Having a pharmaceutical software system, such as O2 Process Manufacturing ERP software, will help you meet the industry challenges by providing clear, accurate and real-time information across your whole enterprise in a central location.

For more information about this pharmaceutical ERP software, visit www.evs-sw.com.