Listings tagged with 'clinical trials' (30)

Phase I GMPs
Phase I GMPs

$150.00

Overview: Early clinical trials are conducted to establish initial safety of a drug. The studies are generally in small number of healthy subjects and use lo...

Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations
Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations

$150.00

Overview: This webinar will discuss FDA's current recommendations on using electronic health records in prospective clinical investigations of human drugs, bio...

LSTI_410x310
LSTI_410x310

$299.00

The Future Of Outsourcing In Clinical Research – Preparing For A Changing Global Landscape Date: December 7, 2016 Time: 1:00pm-2:30pm, EST US Duration: 90-...

LifeScienceTrainingInstitute_Stacked
LifeScienceTrainingInstitute_Stacked

$299.00

Pediatric Clinical Trials: Special Considerations and Requirements RECORDED VERSION Date: October 6, 2016 Time: 1:00pm-2:30pm, EDT US Duration: 90 M...

Medidata_Logo_Color_CMYK-01 x200
Medidata_Logo_Color_CMYK-01 x200

This presentation will discuss the paradigm shift in payment tracking from excel or home-grown systems to more commercial, turn-key technology. Sponsors have hi...

xtalks logo
xtalks logo

The faster you start and execute a clinical trial, the faster a new product is released to market and the longer that drug is commercially-available under paten...

MentorHealth logo MH
MentorHealth logo MH

$139.00

Overview: Participants will learn what constitutes a qualified clinical trial and how to conduct a billing risk assessment on a clinical trial study. A sample t...

Webinar Instructor - Social Media in Clinical Trials
Webinar Instructor - Social Media in Clinical Trials

$189.00

Social media is a great tool that enables companies to highlight specific issues, addressing concerns, educating patients and doctors alike, and engaging multip...

Compliance Global Inc.
Compliance Global Inc.

$155.00

Overview: Because malignant tumours are life-threatening, the death rate from these diseases is high, and existing therapies have limited effectiveness, it i...

Live demo of ClinCapture, Clinovo's open source electronic data capture (EDC) system The development of open source technology in the clinical arena has been...

$189.00

Description Why should you Attend: In the mutli-site cinical studies, it is quite common that one or more sites in several coutnries become high enrolle...

With the ever rising cost and complexity of clinical trials, adaptive design is a promising solution highly regarded by both pharmaceutical companies and regula...

In a recent announcement of the proposed revisions to existing federal regulations governing human research subjects, the US Department of Health and Human Serv...

With the ever rising cost and complexity of clinical trials, adaptive design is a promising solution highly regarded by both pharmaceutical companies and regula...

Open source is becoming more and more prevalent in clinical trials, introducing an innovative way to save costs while keeping high clinical data quality and sec...

Open source is becoming more and more prevalent in clinical trials, introducing an innovative way to save costs while keeping high clinical data quality and sec...

Oracle Clinical (OC) / Remote Data Capture (RDC) 4.6 provides the ability to conduct global clinical trials more efficiently and effectively. The newest release...

Siebel Clinical is well-known as a robust clinical trial management system (CTMS) that streamlines clinical trial management. The system can be operated uniquel...

Trying to build a business case for a clinical trial management system (CTMS) at your organization? Let us help you! BioPharm Systems’ Clinical Trial Manageme...

Achieving complete and efficient reporting of adverse drug reactions is a critical goal for all companies involved in developing and delivering medicinal produc...

$245.00

Overview: The purpose of FMEA is to affect the design and the most practical time to do this is when competing designs are being considered, not after choices h...

$245.00

Overview: There is a pervasive public perception that the FDA has been ineffective in protecting the public. Recent news events in foods, drugs, and devices ...

$165.00

Overview: A comprehensive review of an ideal chemical control program will be presented. The guidelines presented will enable your company to implement progr...

$245.00

Overview: This webinar will cover several recommendations to improve the hospital's Due Diligence when dispensing Schedules II through V controlled substances i...

Site visit and clinical trip reports are part of every clinical trial. In the past few decades, several tools have been developed to streamline the trip report ...

The new ISO Individual Case Safety Report (ICSR) standard is being finalized in 2011. A major revision of the ICH E2B guideline is progressing based on the new ...

Implementation of Oracle Clinical (OC) and Remote Data Capture (RDC) 4.6 provides life sciences organizations with more options for designing clinical trials. T...

Oracle’s Clinical Development Analytics (CDA) is a comprehensive analytics solution that provides life sciences sponsors and CROs operational insight into the...

You've implemented state-of-the-art enterprise systems for different work functions, but they don't talk to each other. Now what? Savvy organizations know how t...

ASCEND On-Demand is a pre-configured and enhanced version of Oracle's Siebel Clinical that uses a software-as-a-service (SaaS) platform. Its subscription-based ...

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