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BEAUFORT
Live/Registered
REGISTERED AND RENEWED

on 07 Mar 2019

Last Applicant/ Owned by

Attn.: Scott Vooss, Dir. of Mktg./Comms.

NORFOLK

VA

23510

Serial Number

77600189 filed on 24th Oct 2008

Registration Number

3690806 registered on 29th Sep 2009

in the Supplemental Register

Correspondent Address

Timothy J. Lockhart

TIMOTHY J. LOCKHART

440 Monticello Avenue, Suite 2200

ATTN.: IP ADMINISTRATOR

NORFOLK, VA 23510-2243

Filing Basis

1. intent to use

2. use application currently

Disclaimer

NO DATA

BEAUFORT

Consulting services in the field of manufacturing compliance and validation, namely, providing technical advice related to the manufacture of pharmaceuticals Regulatory submission management, namely, assisting others in preparing Investigational New Drug applications (INDs) and New Drug Applications (NDAs) for submission to the FDA; database management Legal research, namely, regulatory research Read More

Classification Information


Class [035]
Advertising, Business & Retail Services


Regulatory submission management, namely, assisting others in preparing Investigational New Drug applications (INDs) and New Drug Applications (NDAs) for submission to the FDA; database management


First Use Date in General

25th Jun 2009

First Use Date in Commerce

25th Jun 2009

Class [040]
Treatment & Processing of Materials Services


Consulting services in the field of manufacturing compliance and validation, namely, providing technical advice related to the manufacture of pharmaceuticals


First Use Date in General

25th Jun 2009

First Use Date in Commerce

25th Jun 2009

Class [042]
Computer & Software Services & Scientific Services


Contract research organization (CRO) services, namely, monitoring of clinical trials for investigational drugs of biotech and pharmaceutical companies, clinical trial project management and quality assurance, medical writing of investigational drug protocols, and medical research in the nature of biostatistical analysis; consulting services in the field of conducting clinical trials, drug development, manufacturing environmental compliance and validation, advanced technology in the pharmaceutical field, and medical research in the nature of clinical benchmarking used to improve the performance of professionals in the fields of international health, the pharmaceutical industry, the biotechnology industry and the medical device and diagnostics industries; providing quality assurance services in the field of regulatory submissions to the FDA by life sciences companies to ensure validity and accuracy; product development for others, namely, providing implementation services relating to the development and validation of drugs, devices and biologics


First Use Date in General

25th Jun 2009

First Use Date in Commerce

25th Jun 2009

Class [045]
Personal & Legal & Social Services


Legal research, namely, regulatory research in the pharmaceutical industry, biotechnology industry and the medical and diagnostics industry; consultation in the field of regulatory compliance to ensure validity and accuracy of regulatory submissions to the FDA by life sciences companies; conducting regulatory and compliance audits for others, namely, reviewing standards and practices to assure compliance with laws and regulations in the fields of pharmaceutical, veterinary, pharmacogenomic, biotechnical and medical products and devices; providing information relating to legal affairs, namely, providing regulatory information relating to the development and validation of drugs, devices and biologics; regulatory compliance consulting as it applies to clinical trials, namely, monitoring by clinical research administrators for compliance with regulations governing clinical trials; legal document preparation services, namely, preparation of Investigational New Drug applications (INDs) and New Drug Applications (NDAs) for submission to the FDA; consulting services in the field of regulatory affairs and manufacturing compliance and validation, namely, regulatory compliance consulting as it applies to prescription drug sampling; consulting services in the field of clinical benchmarking and performance improvement, namely, providing independent review of clinical trials involving human subjects in the nature of reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research


First Use Date in General

25th Jun 2009

First Use Date in Commerce

25th Jun 2009

Mark Details


Serial Number

No 77600189

Mark Type

No Service Mark

Attorney Docket Number

No 06887.000

44D Filed

No

44D Current

No

44E filed

No

44E Current

No

66A Filed

No

66A Current

No

Current Basis

No

No Basis

No

Legal History


Show more

Status DateAction Taken
07th Mar 2019REGISTERED AND RENEWED (FIRST RENEWAL - 10 YRS)
07th Mar 2019NOTICE OF ACCEPTANCE OF SEC. 8 & 9 - E-MAILED
07th Mar 2019CASE ASSIGNED TO POST REGISTRATION PARALEGAL
07th Mar 2019REGISTERED - SEC. 8 (10-YR) ACCEPTED/SEC. 9 GRANTED
03rd Feb 2019TEAS SECTION 8 & 9 RECEIVED
29th Sep 2018COURTESY REMINDER - SEC. 8 (10-YR)/SEC. 9 E-MAILED
20th Jun 2016APPLICANT/CORRESPONDENCE CHANGES (NON-RESPONSIVE) ENTERED
20th Jun 2016TEAS CHANGE OF OWNER ADDRESS RECEIVED
25th Sep 2015NOTICE OF ACCEPTANCE OF SEC. 8 - E-MAILED
25th Sep 2015REGISTERED - SEC. 8 (6-YR) ACCEPTED