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  • 3rd International Conference on Transcriptomics

    3rd International Conference on Transcriptomics

    Life Sciences Bangkok (Bangkok) March 13, 2017 Check with publisher

    Conference Series has been instrumental in conducting international Biochemistry meetings for seven years, and very excited to expand Europe, America and Asia Pacific continents. Previous meetings were held in major cities like Philadelphia, Orlando ...

  • Developing drugs for the treatment of neurodegenerative diseases

    Developing drugs for the treatment of neurodegenerative diseases

    PhD Studentships Liverpool December 3, 2016 Check with publisher

    Ageing is arguably the major biomedical challenge of the 21st century with the incidence of age-related diseases, and neurodegenerative diseases in particular, expected to increase dramatically in the coming decades. In model organisms, the process o...

  • 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 EU Clinical Trial Regulation + EU Filings & Registrations 2017

    The EU Clinical Trial Regulation + EU Filings & Registrations 2017

    Quality Control, Safety & Security Zurich, Switzerland (Hilton Zurich Airport) September 21, 2017 1695.00 Dollar US$

    Course "The EU Clinical Trial Regulation + EU Filings & Registrations" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: This course covers the requirements ...

  • 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...

  • 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 ...

  • 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...

  • Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices 2017

    Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices 2017

    Training and Teaching Chicago, IL (Chicago, IL) March 24, 2017 1295.00 Dollar US$

    The changing game for drug and device marketing, however, is governed by antiquated and inadequate rules created for traditional print and broadcast advertising by the Food and Drug Administration ("FDA"). How the FDA will deal with such advanced com...

  • FDA Scrutiny of Promotion and Advertising Practices 2017

    FDA Scrutiny of Promotion and Advertising Practices 2017

    Training and Teaching Minneapolis, MN (Embassy Suites by Hilton Minneapolis Airport) June 15, 2017 1295.00 Dollar US$

    Course "FDA Scrutiny of Promotion and Advertising Practices" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: If you go "off label" with advertising and promoti...

  • 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...

  • FDA's GMP Expectations for Phase I and First-in-Man Clinical Trials 2017 - 50% Discount

    FDA's GMP Expectations for Phase I and First-in-Man Clinical Trials 2017 - 50% Discount

    Training and Teaching Los Angeles, CA (Los Angeles, CA) March 24, 2017 1295.00 Dollar US$

    Early clinical trials are conducted to establish initial safety of a drug. The studies are generally in small number of healthy subjects and use lower doses of the drug product. Therefore, only small amounts of investigational material are required. ...

  • FDA Scrutiny of Promotion and Advertising Practices 2017

    FDA Scrutiny of Promotion and Advertising Practices 2017

    Training and Teaching Chicago, IL ( Chicago, IL) September 21, 2017 1295.00 Dollar US$

    Course "FDA Scrutiny of Promotion and Advertising Practices" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: If you go "off label" with advertising and promoti...

  • FDA Effective Regulatory & Quality Submissions 2017

    FDA Effective Regulatory & Quality Submissions 2017

    Training and Teaching Courtyard Raleigh-Durham Airport ( Raleigh, NC) June 15, 2017 1295.00 Dollar US$

    Course "FDA Legal Writing Skills that Result in Effective Regulatory & Quality Submissions" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Law school prep...

  • 2nd International Conference on Nucleic Acids, Molecular Biology and Molecular Medicine

    2nd International Conference on Nucleic Acids, Molecular Biology and Molecular Medicine

    Molecular Biology Pennsylvania (Philadelphia) March 24, 2017 599.00 Dollar US$

    We are pleased to invite the contributors across the globe on its "2nd International Conference on Nucleic Acids, Molecular Biology & Molecular Medicine" which is slated at Philadelphia, USA during August 31-September 01, 2017 around the theme “E...