Medical consulting - Import export

Geranium essential oil (Geranium macrorrhizum) is extracted from the leaves and flowers of this plant. Geranium is a popular plant in aromatherapy and naturopathy, known for its potential therapeutic properties. However, it is important to note that this information is not a substitute for medical advice. It is always advisable to consult a medical professional before using essential oils for medicinal purposes. Geranium (Geranium macrorrhizum) is a species of plant from the Geraniaceae family, popular among garden and ornamental plants. This herb is known for its diverse species and is used both for decorative purposes and for therapeutic and culinary applications. Although the plant is known as geranium, it should not be confused with geranium (Pelargonium), which is also called geranium and is popular as an ornamental plant crop. Geranium (Geranium macrorrhizum) is a low-growing herbaceous plant characterized by its beautiful flowers and fragrance.

Medical Device Services / Medical Device Laboratory Testing INVITRO-CONNECT GmbH offers you: - General regulatory advice for medical devices - All regulatory examinations and tests under GLP - Project management and study monitoring - Medical Device Regulatory Service - Product testing for contained SVHC substances INVITRO-CONNECT offers you a complete service for the approval of medical devices according (EU) 2017/745 (Medical Device Regulation - MDR) / ISO 10993. From the development of an ideal test strategy to laboratory and project coordination, study monitoring, toxicological expertise and GLP inspections in the cooperation laboratories. We deliver the finalized test reports including the registration dossier - digitally and on paper, worldwide. Benefit from our diverse know-how, our experienced cooperation partners and an international, very well-organized network. Questions? -> contact@invitro-connect.com

The new European Commission’s guidance on persons responsible for regulatory compliance (PRRC) explains that manufacturers, Authorized Representatives and micro and small manufacturers must designate at least one staff member responsible for ensuring compliance to the MDR and/or IVDR as appropriate according to Article 15 of the Regulation. PRRC qualifications are specific for each of these three operators. This does not mean that you have to hire PRRC as employee rather you can avail our PRRC service to overcome the regualtory needs of your company and medical devices – with a consultant managing the system on a few days per month basis. We would be more than happy to discuss this option with you, helping you to find a consultant with the necessary qualifications to perform this service effectively. If you would like to know more about this service, then please contact us.