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
  • 2-day In-person Seminar FDA and U.S. Customs Import Rules and Export Traps in 2020

    2-day In-person Seminar FDA and U.S. Customs Import Rules and Export Traps in 2020

    Quality Control, Safety & Security Washington (Washington, DC) August 8, 2019 2000.00 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...

  • 2-day In-person Seminar Applied Statistics for FDA Process Validation

    2-day In-person Seminar Applied Statistics for FDA Process Validation

    Other Services Philadelphia (Philadelphia, PA) August 8, 2019 2000.00 Dollar US$

    In Guidance for Industry Process Validation: General Principle and Practices, process validation is defined as, ""...the collection and evaluation of data, from the process design stage through commercial production.." The guidance further delineates...

  • 2-day In-person Seminar Death by CAPA - Does your CAPA Program need a CAPA?

    2-day In-person Seminar Death by CAPA - Does your CAPA Program need a CAPA?

    Training and Teaching Philadelphia (Philadelphia, PA) August 8, 2019 2000.00 Dollar US$

    This 2-day seminar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compl...

  • A guide to practical Risk Management - Applying ISO14971 and IEC62304

    A guide to practical Risk Management - Applying ISO14971 and IEC62304

    Training and Teaching Philadelphia (Pennsylvania) May 14, 2019 2000.00 Dollar US$

    Description: Gaps, incorrect or incomplete implementation of safety functionality can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively performed since they are closely linked into the de...

  • PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation

    PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation

    Drug Development san Jose (california) April 20, 2021 1899.00 Dollar US$

    The European Medicines Agency's (EMA) Guideline on good pharmacovigilance practices (GVP), Module IV requires that risk-based audits of the quality system be performed at regular intervals to assure that it complies with the established quality requi...

  • 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...

  • FDA Audit, Quality Assurance Practices, Responsibilities and Expectations

    FDA Audit, Quality Assurance Practices, Responsibilities and Expectations

    Drug Development san Jose (california) April 20, 2021 1699.00 Dollar US$

    This training will examine the differences between Quality Assurance and Quality Control and the responsibilities of each. In addition, attendees will discuss what characteristics quality personnel should possess. The current expectations for an effe...

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

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

    Drug Development san Jose (california) April 20, 2021 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...

  • Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

    Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

    Drug Development san Jose (california) April 17, 2021 1699.00 Dollar US$

    Raw material requirements in a cGMP environment are often overlooked as a Company develops new products. Depending upon the product being developed, e.g., tablets and capsules vs. biotechnology products to include recombinant microorganisms and gene ...

  • 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...