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Top MES Software Company For Pharma Manufacturing Software

Atachi System is the top MES software company for Pharmaceutical manufacturers. We understand the importance of deploying an MES system for Pharmaceutical manufacturers.

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Top MES Software Company For Pharma Manufacturing Software

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  1. Top MES Software Company For Pharma Manufacturing Software

  2. About Pharmaceutical manufacturers Software Pharmaceutical manufacturers are under continuous pressure to remain competitive while meeting the stringent regulatory manufacturing requirements. These manufacturing requirements range from simple electronic record keeping to complex data assuring consistently the reliability of the manufacturing processes, equipment and people’s training, raw material quality, sampling plans, root-cause-analysis, product’s deviations, etc.

  3. About Pharmaceutical manufacturers Software Atachi Systems’ experience in deploying MES for pharmaceutical manufacturing companies for several years in a row is a testimonial on its own. Put simply, Atachi Systems understands the importance of deploying an MES system that is strategic to its core manufacturing requirements, yet cost effective to maintain and run for years to come! Our clients call it the Atachi Advantage.

  4. About Pharmaceutical manufacturers Software Atachi System is the top MES software company for Pharmaceutical manufacturers. We understand the importance of deploying an MES system for Pharmaceutical manufacturers. NGIMES is the “premiere” MES for pharmaceutical manufacturing companies that uses SAP ERP. It helps comply with 21CFR Part 11 electronic signatures, FDA audits, validation and confirms to US FDA cGMP requirements. Furthermore, pharmaceutical companies can take advantage of the cloud based MES (NGIMES) to contain costs while delivering accelerated performance with its in-memory computing platform. Below image covers all the MES functionalities detailed in ISA-95 model that Atachi NGIMES brings.

  5. API stability for Active Pharmaceutical Ingredient Manufacturers Lately few API (Active Pharmaceutical Ingredients) manufacturers have been getting the FDA warning letters for not being able to prove that their API is stable through the stability period. Lot of times the manufacturers face the critical challenges in providing the required documentation that doesn’t tie well into the data integrity of the API stability. There could be various reasons how an API stability got affected and which could have been easily prevented and saved lot of product recalls and avoided the drug shortages into the market. Our below slide gives a simplistic process that could avoid the API stability issues and reduces the FDA audit response times to as low as an hour provided the appropriate system structure is implemented.

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