Intellectual Property Services
Auctorem specializes in intellectual property management and consulting services in areas such as:
- Providing legal advice on intellectual property rights such as the rights of creators or employers and commercial use
- Trademark, Patents Petty, Patents, and Copyright Registration. Objection to trademark registration and appeal of the registrar's order
- Provide legal opinions, checkups, and recommendations to commercial agreements and contracts relating to intellectual property
- Changing or revising trademark information and registration with the Department of Intellectual Property
- Renewal of Trademark, Patents, and Petty Patents Protection
- Civil and criminal intellectual property litigation
Registration of various types of products
Cosmetic products
- Cosmetic formulation checks according to the regulation and requirements of the Food and Drug Administration
- Initial product name verification service to comply with the notification regulation prescribed by the Food and Drug Administration
- Request permission to produce, import or sell cosmetics, register, and renew all types of cosmetic certificates in Thailand
- Label design, Draft and verify the text and product properties on the label including the style and layout of the text Trade names and brands according to the regulation and requirements of the Food and Drug Administration
- Design, create, and review advertising content, media, layout, and descriptions, and to help build a product's marketing point and according to the regulation and requirements of the Food and Drug Administration
- Request for approval of production, import and storage of cosmetics
- Request permission to amend the details of registration, Request for notification of business closure or cancellation of information receipt
Food products and food supplements
- Food and dietary supplements formulation check according to the regulation and requirements of the Food and Drug Administration
- Initial product name verification service to comply with the notification regulation prescribed by the Food and Drug Administration
- Sending for product tests and requesting test results for food products and food supplements, Submitting a safety assessment analysis at an internationally standardized laboratory
- Request permission to produce, import food products and food supplements into Thailand
- Request for food registration/declaration of food details and applying for a license for dietary supplements
- Request for permission to use food labels and request to amend the details
- Label design, draft and verify the text and product properties on the label including the style and layout of the text Trade names and brands according to the regulations and requirements of the Food and Drug Administration
- Request permission to apply for a food production facility that is considered as a factory and does not belong to the factory including requesting to amend various details
- Request for amendment, renewal, and cancellation of various types of licenses and registrations
Medical Device
- Applying for a license to manufacture, import or sell medical devices
- Request for diagnosis of medical device products
- Application for registration of an establishment for manufacturing or importing medical devices
- Request for informing the information of production and import details of medical devices
- Requesting a certificate for the import and export of medical devices
- Application for permission to manufacture medical devices for export and requesting a certificate for the export of medical devices
- Requesting permission to advertise medical devices
- Registration of establishments for manufacturing, importing and storing medical devices
- Renewal of Certificate of Registration and all types of licenses
Hazardous substance
- Registration, renewal, amendment, and cancellation of all types of hazardous substance registration
- Label design, draft and verify the text on the label including the style and layout of the text Trade names and brands according to the regulations and requirements of the Food and Drug Administration
