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  • 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
  • Drug Master Files and Quality Agreement Training Seminar 2018

    Drug Master Files and Quality Agreement Training Seminar 2018

    Drug Development Philadelphia (PA,PA) March 6, 2018 1495.00 Dollar US$

    Overview: This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together. Over time, there have been several misunderstandings be...

  • FDA Guidelines for Pharmaceutical Industry | FDA Regulatory 2018

    FDA Guidelines for Pharmaceutical Industry | FDA Regulatory 2018

    Training and Teaching Chicago, IL ( Chicago, IL) January 19, 2018 1295.00 Dollar US$

    Course "FDA Penalties for Regulatory Non-Compliance in the Pharmaceuticals Industry - 2017 in Review" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: The FDA i...

  • What is Project Management in Pharmaceutical Industry Seminar

    What is Project Management in Pharmaceutical Industry Seminar

    Training and Teaching San Diego, CA (San Diego, CA) November 9, 2017 1295.00 Dollar US$

    Course "Risk Based Project Management for the Life Sciences Industry" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Project management is a discipline that c...

  • Drug Products for Clinical Trials | FDA Approved Drugs List 2018

    Drug Products for Clinical Trials | FDA Approved Drugs List 2018

    Training and Teaching Boston, MA (Boston) January 19, 2018 1295.00 Dollar US$

    Course "Different requirements for Phase I Investigational Drug Products: which GMPs apply since most Phase I drugs are exempt from full GMP requirements and what IND data requirements are necessary as a result?" has been pre-approved by RAPS as elig...

  • Clinical Data Management Seminar 2018

    Clinical Data Management Seminar 2018

    Clinical New Orleans (lousiana) July 5, 2018 1295.00 Dollar US$

    When new drugs or devices are tested in humans, the data generated by, and related to, these trials is 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 ...

  • The EU Clinical Trial Regulation - EU Filings & Registrations

    The EU Clinical Trial Regulation - EU Filings & Registrations

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

    This course covers the requirements for conducting Clinical Studies across the EU via the requirements of the EU Clinical Trial Regulation (for Drugs & Biologics). The course also covers recent updates on EU-GCP associated with the new regulatory...

  • 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...

  • Label Promotion of Drugs and Medical Devices

    Label Promotion of Drugs and Medical Devices

    Training and Teaching Fremont (California) February 22, 2018 290.00 Dollar US$

    Overview: This session sets the context for the off-label promotion of medical products starting with early history and moving to the most recent history of FDA's decision on guidance documents. Why should you Attend: This class presents the latest F...

  • Things To Do Immediately About Master Validation Plan 2019

    Things To Do Immediately About Master Validation Plan 2019

    Quality Control, Safety & Security Fremont (California) November 13, 2018 290.00 Dollar US$

    Overview: How to develop or improve upon a Master Verification and Validation Plan and System that meets U.S. FDA CGMP, ICH Q-series, and ISO 13485 expectations and requirements. Why should you Attend: The billions of dollars spent by industry annual...

  • Verification vs Validation-Product, Equipment and QMS Software

    Verification vs Validation-Product, Equipment and QMS Software

    Drug Development Fremont (California) June 15, 2018 290.00 Dollar US$

    Overview: You will learn What do the U.S. FDA and EU Expect for Verification and Validation, Actions and documentation to meet U.S. FDA CGMP, ICH Q-series, and ISO 13485 expectations and requirements, ISO 14971 and IEC 62366 considerations, as approp...

  • To Facilitate a Closed-Loop Problem Resolution System

    To Facilitate a Closed-Loop Problem Resolution System

    Training and Teaching Fremont (California) November 27, 2017 150.00 Dollar US$

    Overview: Defined Failure Investigation and Root Cause Analysis is a major tool in product complaint, non-conformance, and OOS failure investigations. Why should you Attend: Expectations for meaningful CAPA, supported by results-driven Failure Invest...

  • Fundamentals of Risk Management in Clinical Research 2018

    Fundamentals of Risk Management in Clinical Research 2018

    Quality Control, Safety & Security Fremont (California) March 21, 2018 150.00 Dollar US$

    Overview: The premise behind RBQM is that monitoring quality can be improved by leveraging existing data intelligence. This, in turn, calls for more robust quality assurance (QA) systems focused and efficient resource utilization and allocation at th...