Steps for Registration of a Patent

 Step 1:   Idea or concept (Invention) must be written down with as many details as possible

Step 2:  Drawings, diagrams or sketches explaining the working of the invention must be included while filing the application

Step 3: To check whether the invention is a patentable subject matter or not

Step 4: search for Patentability

Step 5: A patent application needs to be draft by applicant

Step 6: Publication of the application need to be done by the investor

Step 7: Examination request

Step 8: Respond to the objections raised

Step 9: objections must be cleared

Step 10: The final step is the grant of a patent to the inventor 

Documents for Patent Registration

➲ Application in Form -1 which includes all the information related to name and address of inventor, name and address of applicant.

➲ Form-2 which describes the provisional or complete specification, as applicable along with the Drawings or sketches (if any)

➲ The Application form should also indicate clearly the source of the geographical origin of any biological material used in the specification.

➲ Power of attorney or authority letter in favour of the patent attorney enabling him to file the respective patent application on behalf of the inventor.

➲ All patent applications must bear the signature of the applicant or authorized person or Patent Attorney along with date and name.

➲ A copy of a valid Photo ID Proof of the inventor/Owner

➲ A copy of a valid Address Proof of the Inventor

➲ Declaration as to inventorship for applications with complete specification or a convention application.

➲ In case of a Company following additional documents shall be needed

  • Certificate of Incorporation
  • MOA (Memorandum of Association)

➲ In case of a partnership firm following additional documents shall be needed

  • Partnership Deed
  • GST Certificate

Comments

Post a Comment

Popular posts from this blog

Indian Certification for Medical Devices (ICMED 9000 / ICMED 13485)

  Regulation of medical devices and their quality systems in India was limited compared with other developed nations that typically have very robust approval systems for medical devices in place. Together with the Quality Council of India (QCI) and the National Accreditation Board for Certification Bodies (NABCB), the Association of Indian Medical Device Industry (AIMED) has developed a voluntary quality certification scheme for medical devices in India, Indian Certification for Medical Devices (ICMED) It is the country's first indigenously developed quality assurance system mandatory for all medical devices marketed in the nation. This was proposed in a recent meeting called for the drafting of (separate) rules for medical devices with government officials with a special focus on drafting regulatory framework for the granting of medical device manufacturing licenses. The meeting discussed how to proceed with the registration of manufacturers and importers of medical devices on an...
Read more

EPR Authorisation (Plastic Waste)

Image
  Plastic has many uses, and due to its physical and chemical properties leads to huge commercial use and success. The indiscriminate disposal of plastic has, however, become a major environmental threat. In particular, plastic carrying bags are the main contributors to littered waste and, every year, millions of plastic bags end up in the atmosphere vis-à-vis the soil, water bodies, rivers, etc it takes an average of one thousand years to decompose completely. Therefore, the Plastic Waste (Management and Handling) Regulations, 2011 were notified in 2011, which included plastic waste management, to tackle the problem of scientific plastic waste management. In violation of the earlier Plastic Waste (Management and Handling) Regulations, 2011 the government notified the  Plastic Waste Management Regulations, 2016 Objective of Extended Producer Responsibility   ➲  Increase the minimum thickness of plastic carry bags from 40 to 50 microns and specify a minimum thick...
Read more