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  Mpharma® - Pharmaceutical Expert System
 
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Developments in science and technology, the high costs of research and development, changes in product markets, intense competition, the growth in counterfeiting, the tightened regulatory compliance, ever-changing legislations, the risks of global pandemics all make up the challenging landscape that is the pharmaceutical and life sciences sector. Further, with the increasing difficulty of finding and developing new drugs, the pressure to innovate and launch new products is tremendous.
   
 

It is against this backdrop that applying new technologies to achieve business advantage is of vital importance, and what makes the leader stay ahead of the pack.
 
MPHARMA provides you with the necessary global resources & technologies to improve your manufacturing and distribution processes. Tapping into our vast domain knowledge, we work with our clients across the value chain, from the specialist areas of research and development and clinical trials, to expertise in optimizing manufacturing systems and marketing services.

The pharmaceutical Industry is an ever-growing industry with a more than US$500 Billion market, wherein time is of greatest essence. Big industry players of the world spend billions of dollars in drug research and development. A typical drug takes almost 12-16 years from conception to delivery and hundreds of millions of dollars.

A lot of time and money is spent on initial research, discovery, pre-clinical trials, clinical trials and so on. Based on the success of clinical trials, penetration through Marketing and Sales plays a major role but takes comparatively less time. Full-scale manufacturing is a highly challenging process as it involves innumerable steps with lots of intermediate testing at each stage. Since it is critical to produce a drug correctly with all the chemical, physio-chemical, micro-biological and various other characteristics devised by the regulatory body along with hundreds of critical environmental parameters coming into play during the manufacturing process, it is essential to produce the drug accurately by adhering to all the norms of the starting material, API (Active Pharmaceutical Ingredient) supported with firm guidelines and checkpoints for the entire manufacturing cycle.

All these are supported with 21st century GMP - Good Manufacturing Practices (which acts like a standard for manufacturing of drugs in the Pharmaceutical Industry). Since time has been a great challenge in the drug development process with the expectation of high precision data at all stages of drug manufacturing, a huge endeavor is envisaged to automate the process.

Keeping in view the above objective, MGRM Net has developed “MPHARMA” a state-of-art application to cater to all the stages of drug Manufacturing process supported with the completely integrated Industry practices adhering to the Best Practices of e-enabled Quality norms.

The benefits of integrating Manufacturing, Industry and Quality is as follows:

   
 
Efficient Planning & Scheduling
E-Work Allocation & Progress Monitoring
Minimal Manual Data Entry
Plant wide availability of data
Short Processing Time of Information Flow
Online Machine Availability Status
Optimum Machine Utilization
Reduction in Production Loss
Raw Material Pilferage Time Loss vs. Quantitative Loss Analysis
In Process Material Flow Control
Methodical In Process Control
Standardized Information Flow and Checkpoint Control Mechanism
Plant wide Most Current Information
Integration between Plant, Stores, Maintenance, Quality and Finance
Continuous Performance Optimization
Constant Product Quality
Event Documentation
Streamlined Administrative Processes
Efficiency & Transparency in each activity
Objective Information - Process wise, Manpower wise
Reduction of misinformation / Lack of timely information
Key Critical Performance Graphs
Internal Messaging System
Alerts
Proactive Decision Support System
e-Compliance Reporting
Efficient Manufacturing Execution System
   
 

And more...

For more information, email us at contact@mgrmnet.com

 
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