Allurmed was established in 2018 to provide professional regulatory and consulting services to the pharmaceutical, medical device and healthcare sectors.

Since the beginning of our operations, our main objective has been to become a reliable and long-term partner for pharmaceutical manufacturers, medical device companies, distributors, importers and organisations involved in healthcare projects.

Over the years, Allurmed has expanded its service portfolio and developed an integrated service model covering medicinal product registration, medical device registration, biologically active food product registration, pharmacovigilance, regulatory consulting and medical facility design.

Our professional approach

Allurmed’s work is not limited to the preparation and submission of documents. Each product and project is individually assessed from scientific, technical and regulatory perspectives.

Our team identifies potential risks, detects documentation gaps and develops an appropriate regulatory strategy based on the client’s objectives and the requirements of the relevant market.

We provide professional support in the following areas:

• medicinal product registration and regulatory support;
• medical device classification and registration;
• registration and expert assessment of biologically active food products;
• establishment and management of pharmacovigilance systems;
• ICSR, PSUR/PBRER, RMP and PSMF services;
• assessment of registration dossiers and technical documentation;
• adaptation of labels, packaging materials and instructions for use;
• professional medical and pharmaceutical translations;
• functional planning of clinics, laboratories and manufacturing facilities;
• market-access and regulatory-strategy development.

Our mission

Our mission is to facilitate market access for pharmaceutical, medical and healthcare products by providing transparent, reliable and professional regulatory services.

We support our clients not only in obtaining registration documentation, but also in establishing sustainable and compliant regulatory systems.

Our values

Professionalism
Systematic and responsible management of every project by experienced specialists.

Transparency
Clear communication with clients regarding project stages, potential risks and completed activities.

Scientific approach
Decisions based on technical documentation, scientific evidence and applicable regulatory requirements.

Confidentiality
Protection of commercial, technical and regulatory information related to clients and their products.

Long-term partnership
Building continuous cooperation rather than limiting our relationship to a single project.

Allurmed today

Today, Allurmed operates as a professional consulting company managing projects of varying complexity in pharmaceutical regulation, medical devices, biologically active food products, pharmacovigilance and medical facility design.

Our goal is to continuously develop in line with the changing regulatory environment, improve the quality of our services and become a trusted international partner for our clients.

Allurmed — professionalism, scientific expertise and trusted partnership.