Top MES Software Company For Pharma Manufacturing Software

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Top MES Software Company For Pharma Manufacturing
Software
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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 peoples
  training, raw material quality, sampling plans,
  root-cause-analysis, products deviations, etc.

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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.

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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.

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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 doesnt 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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