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Investigación Legal y Escritura

Documentation

  • Review of ingredients raw materials and formulations according to regulatory requirements

  • Responsible statement

  • Notification on the European portal (CPNP)

  • Preparation of the product information file (PIF - part A)

  • Safety assessment (PIF - part B)

  • Technical data sheets amd material safety data sheets (TDS / MSDS)

  • Labeling review and adaptation to CLP Regulation 1272/2008

  • Answers for Deficiency Letters of Regulatory Authorities

  • Spanish national parapharmacy code

  • Regulatory consultancy

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