Drawing for BRIDGEWARE

USPTO serial 50175647

BRIDGEWARE

Reviewed by CopyMark Law Group

Filing date
Status date
Registration date
—
Examiner
—
Law office
—

What this means

Status 630 means your trademark application is in the USPTO queue and has not yet been assigned to an examining attorney. This is normal shortly after filing. Examination typically begins within three to four months, though timing varies. Wait for assignment and the first examiner action. Monitor TSDR monthly for status changes to 638 (assigned) or an office action.

Status 630: Status 630 means your trademark application is in the USPTO queue and has not yet been assigned to an examining attorney. This is normal shortly after filing. Examination typically begins within three to four months, though timing varies.

Need help with BRIDGEWARE?

If you own this trademark, we can monitor new filings and help with USPTO deadlines. If you do not, we can file a new U.S. application.

Current trademark owner
Monitor this mark, or talk with CopyMark about this registration.
Not the owner?
File a new U.S. trademark application, or speak with our attorneys.

Owner

Goods and services

ClassDescriptionStatusFirst use
035Technology-enabled business consulting and advisory services in the fields of medical device, pharmaceutical, biotechnology and life sciences research and development, product development, clinical development, clinical research operations, clinical trial planning and management, product lifecycle strategy and commercialization; business project and program management services for others in the fields of research, product development and clinical research; business management and operational consulting relating to the planning, coordination, management and oversight of clinical trials and product development programs; business intelligence services and business data analysis relating to research, product development, clinical operations and commercialization.ACTIVE—
041Educational services, namely, providing technology-enabled training, courses, seminars, and workshops in the fields of medical device, pharmaceutical, biotechnology, and life sciences research and development, product development, product lifecycle management, regulatory affairs, quality management, clinical development, clinical research, clinical trial planning and operations, evidence generation, data analytics, artificial intelligence, and clinical research technology.ACTIVE—
042Technology-enabled scientific research and development in the medical device, pharmaceutical, biotechnology and life sciences fields; conducting clinical trials for others; professional scientific and clinical research consulting relating to R&D, product development, clinical development and evidence generation; providing non-downloadable software and AI technology for planning, executing, monitoring and analyzing R&D, product development, clinical research and lifecycle activities, including workflow automation, data analysis, risk identification, predictive analytics, decision support, insights, and management of clinical, regulatory, quality, safety and evidence data and workflows.ACTIVE—
045Technology-enabled regulatory compliance consulting services in the medical device, pharmaceutical, biotechnology, and life sciences industries; regulatory compliance consulting relating to research and development, product development, clinical research, clinical trials, quality systems, evidence generation, commercialization, and product lifecycle activities; reviewing standards and practices to assure compliance with laws and regulations in the fields of healthcare products, life sciences, and clinical research.ACTIVE—

Related trademarks

CopyMark links this record to cited §2(d) serials, the owner's other marks, Nice classes, similar mark names, and recently changed USPTO applications.

Prosecution history

DateCodeEventWhat it means
Oct 22, 2026MAFRAPPLICATION FILING RECEIPT MAILED—
Oct 22, 2026NWAPNEW APPLICATION ENTERED—

Frequently asked questions

Related guidance