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3rd International Conference on Transcriptomics
Life Sciences Bangkok (Bangkok) March 13, 2017 Check with publisherConference 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 ...
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Developing drugs for the treatment of neurodegenerative diseases
PhD Studentships Liverpool December 3, 2016 Check with publisherAgeing 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...
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DrugAge database of compounds that increase lifespan
Biomedical Sciences Liverpool August 24, 2015 Check with publisherWe'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
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Label Promotion of Drugs and Medical Devices 2018
Training and Teaching Fremont (California) April 19, 2018 FreeOverview: 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 session will discuss commen...
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Clinical Data Management - Benefits of Standardization in Establishing CDM Processes
Pharmacology - Drug Development Philadelphia (pennsylvania) April 2, 2018 Check with publisherCourse "Clinical Data Management" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: When new drugs or devices are tested in humans, the data generated by, and re...
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Promotion & Advertising Practices 2018 under FDA Observation
Medical - Health Philadelphia (pennsylvania) April 2, 2018 Check with publisherCourse "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...
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Phase I Investigational Drug Products | USA Seminar 2018
Pharmacology - Drug Development Salt Lake city (Utah) April 2, 2018 Check with publisherCourse "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...
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Expectations for Products Used in Early Phase
Drug Development Fremont (California) March 21, 2018 150.00 Dollar US$Overview: This presentation will review the GMP guidance document and discuss how it may be integrated with the recommendations of the guidance documents on CMC requirements. Areas Covered in the Session: Discussion of the elements found in the guida...
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Fundamentals of Risk Management in Clinical Research 2018
Quality Control, Safety & Security Fremont (California) March 21, 2018 150.00 Dollar US$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...
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GMP Regulations and How it Apply to Analytical Laboratories
Clinical Fremont (California) March 21, 2018 150.00 Dollar US$Overview: Auditing analytical laboratories can be complex because of the preparation that is often required. All of the GMP rules do not apply to the laboratory; while there may be additional requirements depending upon the type of testing that is be...
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Drug Master Files and Quality Agreement Training Seminar 2018
Drug Development Philadelphia (PA,PA) March 6, 2018 1495.00 Dollar US$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...
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Label Promotion of Drugs and Medical Devices
Training and Teaching Fremont (California) February 22, 2018 290.00 Dollar US$Overview: This session sets the context for the off-label promotion of medical products starting with early history and moving to the most recent history of FDA's decision on guidance documents. Why should you Attend: This class presents the latest F...
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Discussion on Raw Material Methods and Specifications
Medical Sciences Fremont (California) February 22, 2018 Check with publisherOverview: Based on knowledge of the active and inactive ingredient's function and role in the finished dosage form, Compendia methods and specifications are clearly accepted by third parties and regulatory agencies. Why should you Attend: The FDA has...
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GMP for Phase I Investigational Drug Products 2018
Training and Teaching Fremont (California) January 24, 2018 150.00 Dollar US$Overview: Phase I clinical trials are the first time that investigational new drugs are introduced into human subjects and, although it is very, very important for all drugs to be manufactured using GMPs, it is probably more important than at any oth...
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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...
