Consulting

Licensing

Wholesalers - Pharmacies - Sale of non-prescription medicines - Clinics

Preparation and follow-up of applications to Regulatory Authorities

Human Medicines

Development

Preparation and management of Marketing Authorisations (MAs)

Support

Update of MA dossier

Evaluation

Translation and review of Summary of Product Characteristics (SmPC), Package Information Leaflet (PIL) and Label

Preparation

Expert reports

Medical Devices

Preparation

Technical dossier and related documentation

Evaluation

Labelling, Package information leaflet, Certificate of Conformity and CE Certificate

Notification to Regulatory Authorities

Request to assignment of MD national code

Support

Launch of MD to the market

Cosmetics and Personal Care Products

Preparation

Technical documentation

Evaluation

Labelling (method of presentation of ingredients and mandatory mentions)

Registration

Notification of Cosmetic products on CPNP Portal

Food Supplements

Preparation

Technical documentation

Evaluation

Labelling (method of presentation of ingredients and mandatory mentions)

Notification to Regulatory Authorities

Regulatory support and market introduction