a way to benchmark compliance, improve processes and keep up with the pace of business.
How do we avoid Quality and Compliance Oversights?
How do we stay in line with Good manufacturing practices (GMP)?
Budgets have decreased for R&D due to pricing norms leading to low profitability in a highly volatile market?
How do we bring in cutting edge ideas, convert them into implementable business processes, encouraging continuous innovation extending far beyond Intellectual Property Rights (IPR) for a product?
All such questions above are generally faced by most pharmaceutical companies.
At a corporate level, quality and compliance management in heavily regulated pharmaceutical environments is a tricky endeavor. After all, success in the areas of quality and compliance can only be achieved when a multitude of variables are controlled and continually maintained. From document control to CAPA control, and from audit to CRO management, quality and compliance, to avoid oversights, requires full attention and/or automation over all pertinent details.
Key Benefits
Holistic approach, consolidating, integrating and streamlining all the business processes, helping to keep track of sensitive functions, such as:
Compliance with legal regulation.
Formulation and Recipe management.
Real-time bi-directional material traceability.
Batch tracking in WIP, and Yield reconciliation.
Lot Management.
Effective management of BMR/BPR as per GMP.
Wastage elimination through expiry management.
In Process Quality Control (IPQC) system, Inspection and certificate analysis.
Shorten production cycles, maintaining high quality standards across processes and optimize the use if resources.
Single source of centralized data, effective and clear analytical reporting, leading to quick decision making.
for more information: http://www.eresourceerp.com/news/lifescience_erp_software_is_helping_drive_the_change
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