Atlas Pharma Inc. offers its customers the ability to perform stability studies of their products, under storage conditions compliant with GMP and ICH (International Conference on Harmonisation)
Our storage facilities are validated fort temperatures between 25 ° C to 40 ° C and, where appropriate,  humidity  control at 60% RH and 75% RH with many intermediates options available.
All stability chambers are controlled by a management system that records temperature and humidity continuously and notifies the appropriate personnel if the predetermined alarm criteria are met.
Atlas Pharma has an experienced staff who can provide a range of stability testing services, including routine analysis.
See in what follows our full range of the stability program:
  • protocol development studies
  • Storage of products
  • Analytical testing
  • Data Management
  • Statistical analysis of data
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QUALITY CONTROL

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The Atlas pharma has created an effective and rigorous quality control system for ...
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STABILITY STADIES

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Atlas Pharma offers its customers the ability to perform stability studies of their products...
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VALIDATION

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"The purpose of the validation of an analytical procedure is to demonstrate that it matches ...
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R & D

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The research and development department is to create new methods of analysi...
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