Intalyse Trademark (Class 9) — Send To Vienna Codification Status & Details

The current status of Intalyse is "Send To Vienna Codification". It was filed on 30/09/2026 at DELHI in Class 9. Status may change over time as the application moves through examination, publication, opposition and registration stages.

Intalyse is filed in Class 9, covering: Downloadable and recorded computer software platforms, including customer-hosted and on-premises deployable software, for artificial intelligence based pharmacovigilance, drug safety, medical device safety, product safety and life sciences data analytics; downloadable and recorded computer software for adverse event intake, product complaint intake, individual case safety report (ICSR) processing support, ICSR validity assessment, duplicate case screening, case triage, E2B R3 data mapping, medical coding support, literature monitoring, PubMed and biomedical literature ingestion, article review, safety signal support, social and digital media safety monitoring, social media post and comment classification, signal detection support, signal management, regulatory intelligence, workflow management, audit trail management, electronic records management, electronic signature support, role-based access control, tenant configuration, compliance evidence management, validation evidence management and regulatory data analysis; downloadable and recorded artificial intelligence software for extracting, classifying, mapping, summarizing, translating, coding and reviewing safety-related data, adverse event information, product complaint information, medical literature, social media content, digital media content, emails, documents, attachments, source evidence and regulatory information; downloadable computer software for managing controlled prompts, AI agent workflows, human-in-the-loop review, reviewer decisions, audit logs, quality records, safety evidence packages and regulated life sciences workflows; downloadable databases and electronic data files in the fields of pharmacovigilance, drug safety, medical device safety, product safety, medical coding, literature monitoring, social media monitoring, signal management, regulatory compliance and audit readiness; downloadable electronic publications, namely user manuals, technical documentation, standard operating procedure templates, validation protocols, compliance templates, product documentation and training materials in the fields of pharmacovigilance, drug safety, medical device safety, artificial intelligence governance and regulated life sciences software.; Downloadable and recorded computer software platforms, including on-premises and customer-hosted software, for artificial intelligence based pharmacovigilance, drug safety, medical device safety, life sciences data analytics, adverse event intake, product complaint management, ICSR processing support, literature monitoring, social and digital media safety monitoring, signal management, regulatory intelligence, audit trail management, workflow management, compliance evidence management and regulated life sciences data analysis; downloadable artificial intelligence software for extraction, classification, mapping, summarization and review of safety-related data, medical literature, social media content, product complaints and regulatory information.

Intalyse covers: Downloadable and recorded computer software platforms, including customer-hosted and on-premises deployable software, for artificial intelligence based pharmacovigilance, drug safety, medical device safety, product safety and life sciences data analytics; downloadable and recorded computer software for adverse event intake, product complaint intake, individual case safety report (ICSR) processing support, ICSR validity assessment, duplicate case screening, case triage, E2B R3 data mapping, medical coding support, literature monitoring, PubMed and biomedical literature ingestion, article review, safety signal support, social and digital media safety monitoring, social media post and comment classification, signal detection support, signal management, regulatory intelligence, workflow management, audit trail management, electronic records management, electronic signature support, role-based access control, tenant configuration, compliance evidence management, validation evidence management and regulatory data analysis; downloadable and recorded artificial intelligence software for extracting, classifying, mapping, summarizing, translating, coding and reviewing safety-related data, adverse event information, product complaint information, medical literature, social media content, digital media content, emails, documents, attachments, source evidence and regulatory information; downloadable computer software for managing controlled prompts, AI agent workflows, human-in-the-loop review, reviewer decisions, audit logs, quality records, safety evidence packages and regulated life sciences workflows; downloadable databases and electronic data files in the fields of pharmacovigilance, drug safety, medical device safety, product safety, medical coding, literature monitoring, social media monitoring, signal management, regulatory compliance and audit readiness; downloadable electronic publications, namely user manuals, technical documentation, standard operating procedure templates, validation protocols, compliance templates, product documentation and training materials in the fields of pharmacovigilance, drug safety, medical device safety, artificial intelligence governance and regulated life sciences software.; Downloadable and recorded computer software platforms, including on-premises and customer-hosted software, for artificial intelligence based pharmacovigilance, drug safety, medical device safety, life sciences data analytics, adverse event intake, product complaint management, ICSR processing support, literature monitoring, social and digital media safety monitoring, signal management, regulatory intelligence, audit trail management, workflow management, compliance evidence management and regulated life sciences data analysis; downloadable artificial intelligence software for extraction, classification, mapping, summarization and review of safety-related data, medical literature, social media content, product complaints and regulatory information.

The exact word "Intalyse" is already on record at the Indian Trademark Registry under Application No. 8032450. If you intend to use a similar mark for similar goods or services, you should conduct a comprehensive availability search and consult a trademark attorney before filing. Registerkaro offers a free availability check followed by professional filing.

Indian registered trademarks are valid for 10 years from the date of registration and can be renewed indefinitely in 10-year blocks. Intalyse (App #8032450) is currently in status "Send To Vienna Codification" — renewal dates apply only after registration is granted.

If Intalyse is in the "Advertised before Acceptance" or "Accepted & Advertised" stage, you have a 4-month window from publication in the Trade Marks Journal to file an opposition (Form TM-O) at the same Trade Marks Registry office. Grounds typically include prior rights, descriptiveness or bad faith. Registerkaro can prepare and file a Notice of Opposition for you.