Regulatory Services in Latvia, Regulatory Services

Regulatory services in Latvia for the pharmaceutical industry assist companies in navigating the country's regulatory framework to ensure compliance with European Union (EU) and local regulations. These services include support for the registration of medicinal products with the State Agency of Medicines (SAM) in Latvia, as well as preparing and submitting Marketing Authorization Applications (MAAs). They also help with regulatory compliance for clinical trials, labeling, and post-market surveillance in line with EU directives. Professional services guide pharmaceutical companies through the complexities of obtaining product approval and maintaining market access. Additionally, they assist with regulatory reporting, pharmacovigilance, and adherence to Latvian and EU pharmaceutical laws.