Review of ingredients raw materials and formulations according to regulatory requirements

Preparation of the product information file (PIF – part A)

Safety assessment (PIF – part B)

Preparation of technical data sheets and safety data sheets (TDS / MSDS)

Labeling review and CLP 1272/2008 compliance

Notification in the European portal (CPNP)

Responsible Declaration (AEMPS)

Answers for Deficiency Letters of Regulatory Authorities

Spanish national parapharmacy code

Regulatory consultancy