The trademark application Biopharma Excellence by PharmaLex was filed by PharmaLex GmbH, a corporation established under the laws of the Federal Republic of Germany (the "Applicant"). The application was published for oppositions on May 24, 2021, and it was registered by office on August 30, 2021 without any oppositions.
The application was filed in English (German was selected as the second language).
Change of name and professional address of the trademark registration was recorded on October 17, 2022.
Goods And Services
The mark was filed in class 9 with following description of goods:
Software
Automation software
Artificial intelligence apparatus
Information technology apparatus
Computers
Computer programs for data processing
Computer software applications, downloadable
Unified communications software
Assistive software.
The mark was filed in class 35 with following description of goods:
Advertising, management for others, business administration
Business efficiency expert services
Systemization of information into computer databases
Compilation of information into computer databases
Support and advice in the context of drug distribution in retail and wholesale
Providing outsourced office functions services for drug approval, manufacturing, distribution, security and monitoring
Assistance and consultancy in the context of the retailing and wholesaling of medicines
Consultancy services in the fields of controlling and managing information and implementing and managing databases.
The mark was filed in class 42 with following description of goods:
Scientific and technological services and research and design relating thereto
Scientific, technological, medical and pharmaceutical research and development services
Industrial analysis and research services
Research and development of new products for others
Pharmaceutical drug development services
Research and development of pharmaceutical preparations
Research and analysis services
Biological research
Clinical research
Providing medical and scientific research information
Provision of surveys [scientific]
Scientific laboratory services
Medical research laboratory services
Laboratory research services relating to pharmaceuticals
Research and development in the field of biotherapeutics
Consulting services in the fields of biotechnology, pharmaceutical research and development and genetic science
Scientific research in the fields of pharmaceuticals, vaccines, medicine, biologics, biotherapeutics, biosimilars, therapeutics
Development of a web application for entering and evaluating informative texts for pharmaceuticals and medical products, in particular instructions for use, package inserts, specialist information and for the provision of various documents
Database services, namely storage of data in computer databases
Conversion of data or documents from physical to electronic media
Testing, inspection or research of pharmaceuticals and medicines
Design, engineering, research, development and testing services
Research in the field of gene therapy
Quality assurance, quality control and quality management consultancy
Research services relating to scientific work
Preparation of scientific analyzes and evaluations
Pharmaceutical product evaluation
Consultancy pertaining to pharmacology
Consultancy relating to research and development in the field of therapeutics
Consultancy relating to laboratory testing
Pharmaceutical products development
Development of pharmaceutical preparations and medicines
Testing of pharmaceuticals
Provision of information and data relating to medical and veterinary research and development
Inspection of pharmaceuticals
Scientific investigations for medical purposes
Conducting early evaluations in the field of new pharmaceuticals
Medical laboratory services
Information technology services for the pharmaceutical and healthcare industries
Scientific evaluation of drug efficacy
Services for assessing the efficiency of pharmaceuticals
Analysis and evaluation of product design
Analysis and evaluation of product development
Quality control testing
Materials testing and evaluation
Product safety testing
Certification [quality control]
Quality testing of products for certification purposes
Support and advice on drug safety and monitoring
Consultancy services for the development and approval process of biological samples or chemical samples for therapeutic and diagnostic purpose
Consultancy services in the field of design, planning, implementation and project management of clinical trials, pharmacovigilance, pharmaceutical and biotechnology product development
Consultancy services in the fields of biotechnology, pharmaceutical research and development, laboratory testing and pharmacogenetics
Laboratory analysis service relating to the diagnosis and treatment of persons.
The mark was filed in class 44 with following description of goods:
Medical and veterinary services
Pharmacy advice
Providing information relating to the preparation and dispensing of medications
Provision of pharmaceutical information
Provision of information relating to medicine
Consultancy and information services provided via the Internet relating to pharmaceutical products
Consultancy and information services relating to pharmaceutical products
Consultancy and information services relating to biopharmaceutical products
Advisory services relating to pharmaceuticals
Medical, diagnostic and pharmaceutical services and advice
Medical and pharmaceutical consultancy
Medical services relating to the diagnosis and treatment of persons
Medical analysis and examinations
Medical treatment services
Medical services
Medical screening
Medical monitoring, testing, inspection and analysis services relating to the diagnosis and treatment of illnesses
Medical, diagnostic and pharmaceutical services and advice in the field of drug safety
Providing information in the field of pharmacovigilance and adverse event reporting.
The mark was filed in class 45 with following description of goods:
Regulatory compliance auditing
Regulatory compliance consulting services
Regulatory support and advice in the context of drug approval
Submission of documents, reports and records required for drug approval by regulatory authorities (Regulatory compliance auditing)
Consultancy services in the fields of regulatory compliance and oversight
Advisory services relating to regulatory affairs
Regulatory maintenance of marketing authorizations following approval.