Premium listings
  • Characterization and functional analysis of a novel cancer-associated gene

    Characterization and functional analysis of a novel cancer-associated gene

    PhD Studentships Liverpool May 15, 2016 Check with publisher

    Genes involved in common biological processes and diseases tend to be co-expressed. Therefore, genes co-expressed with known disease-associated genes will help identify new candidates for further studies. Our lab has recently developed a co-expressio...

  • Expertise in genomics and transcriptomics

    Expertise in genomics and transcriptomics

    Data Analysis - Analytics August 24, 2015 Check with publisher

    I lead the Integrative Genomics of Ageing Group (http://pcwww.liv.ac.uk/~aging/), and I have extensive experience in data analysis and integration of multidimensional data. Although my lab’s research integrates different strategies, its focal point i...

  • DrugAge database of compounds that increase lifespan

    DrugAge database of compounds that increase lifespan

    Biomedical Sciences Liverpool August 24, 2015 Check with publisher

    We're starting a new database of drugs and compounds (including natural products) with anti-ageing properties that extend longevity in model organisms. The database will be called DrugAge, and although we have some data already, we are looking for da...

Listings
  • The Veterinary Drug Approval Process and FDA Regulatory Oversight

    The Veterinary Drug Approval Process and FDA Regulatory Oversight

    Drug Development san Jose (california) December 18, 2020 1899.00 Dollar US$

    The U.S. Food and Drug Administration’s Center for Veterinary Medicine (CVM) is responsible for the approval of veterinary drug products intended for family pets, food-producing animals, and other animal species. This seminar will cover the process f...

  • Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs)

    Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs)

    Drug Development san Jose (california) December 18, 2020 1899.00 Dollar US$

    The globalization of the pharmaceutical supply chain has resulted in the increased use of Contract Manufacturing Organizations (CMOs). The use of CMOs provides many benefits; however, it also presents unique compliance risks, particularly since opera...

  • Lifecycle Management of Analytical Methods and Procedures according to new USP and ICH Guidelines

    Lifecycle Management of Analytical Methods and Procedures according to new USP and ICH Guidelines

    Drug Development san Jose (california) December 19, 2020 1699.00 Dollar US$

    Results of analytical methods are used as the basis for important decisions during development and manufacturing of pharmaceutical products. All regulatory agencies expect the regulated industry to have procedures in place to ensure suitable levels o...

  • Designing and Sustaining New and Existing Product Stability Testing Program

    Designing and Sustaining New and Existing Product Stability Testing Program

    Drug Development san Jose (california) December 18, 2020 1699.00 Dollar US$

    This Virtual Seminar will provide a great resource to Pharmaceutical, Biotechnology, Diagnostics, Cell Therapy, Drugs, Biologics, OTC, Radio-pharmaceutical, Pharmacies and Medical Device Industries in understanding the effective way to establish a ne...

  • Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers

    Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers

    Data Management san Jose (california) December 18, 2020 1699.00 Dollar US$

    This course will educate you about various key elements of sterility assurance and contamination control such as Cleanroom Regulations, Classification, Sources and types of particles, Design Requirements, Validation/Qualification, Operations, Environ...

  • Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation)

    Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation)

    Drug Development san Jose (california) November 28, 2020 1699.00 Dollar US$

    The Process Validation Guidelines (January 2011) and the EU Annex 15: Qualification and Validation (October 2015) outline the general principles and approaches the two regulatory bodies consider appropriate elements of process validation for the manu...

  • Biostatistics for the Non-Statistician

    Biostatistics for the Non-Statistician

    Clinical san Jose (california) December 18, 2020 1499.00 Dollar US$

    This seminar is a thorough review of the basics for those who need a refresher on statistical theory and types of statistical analyses. It gives you the information and skills necessary to understand statistical concepts and findings as it applies to...

  • FDA and U.S. Customs Import Rules and Export Traps in 2020

    FDA and U.S. Customs Import Rules and Export Traps in 2020

    Training and Teaching Washington (District of Columbia) February 5, 2020 999.00 Dollar US$

    FDA and the Customs and Border Patrol Service (CBP) have become increasingly sophisticated and equally demanding in the submission of import information and adherence to government procedures. Firms that fail to understand and properly execute an imp...

  • Medical Claims Boot Camp

    Medical Claims Boot Camp

    Drug Development Fremont (California) August 7, 2020 545.00 Dollar US$

    This course covers the fundamentals of medical billing, coding, and reimbursement by explaining how all of these components work together. Emphasis will be placed on the practical application of the latest industry knowledge and standards, with the g...

  • Validation and 21 CFR Part 11 Compliance of Computer Systems

    Validation and 21 CFR Part 11 Compliance of Computer Systems

    Data Management Fremont (California) July 3, 2019 545.00 Dollar US$

    This course is appropriate for beginner and experienced person alike. The topics will build on each other and will give you the latest trends in our heavily regulated industry and how to make it easy for yourself while still achieving data integrity....

  • Texting and E-mail with Patients - Meeting Patient Requests within the HIPAA Rules

    Texting and E-mail with Patients - Meeting Patient Requests within the HIPAA Rules

    Training and Teaching Fremont (California) July 3, 2019 545.00 Dollar US$

    E-mail has long been a staple of people's lives, but as we move into the new digital age, it seems everyone is moving to a new smart phone and wants to use it in all the incredible ways it can be used for health care purposes, including the use of e-...

  • 6-Hour Virtual Seminar on Clinical Data Management - Part II

    6-Hour Virtual Seminar on Clinical Data Management - Part II

    Quality Control, Safety & Security Fremont (California) July 3, 2019 545.00 Dollar US$

    When new drugs or devices are tested in humans, the data generated by, and related to, these trials are known as clinical data. This data represents a huge investment by the biopharmaceutical or device company and is one of its greatest assets. It is...