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Aptys Pharmaceuticals becomes a registered GMP laboratory.

May 19th, 2017: Aptys has been granted the GMP status by the French Agency (ANSM) for quality control of human medicinal products and human investigational medicinal products

This new status acknowledges the high quality level of Aptys. It allows to extend its historical offer, e.g. design of formulations and analytical methods, to quality control of commercial as well as clinical products.

Letter of authorization from the French Agency

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Since 2002, as a contract research and development organization, we offer to our customers:

  • Custom-made formulation and complex generic development
  • Quality control and ICH stability, analytical development and validations
  • Production assistance

The labs are equipped for the design, control and stability studies of solid dosage forms as well as liquid and semi-solid dosage forms.

Formulation

NCE, generics, life cycle managment, scale-up

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Analytics

Quality control, stability, development, validation

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Production assistance

Transfer, scale-up, qualification

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