Listings for Pharma Webinars (61)
$249.00
Design Inputs – Design Outputs Traceability Matrix – Principles...
Live Webinar on Thursday, February 14, 2013 Duration: 90 minutes If your design and manufacturing resources are spending too much time on documentation and ...
$299-399
Market Access, Pricing and Reimbursement Strategies (Focus: BRAZIL, RUSSIA,...
Aligning Your Company Assets with the BRC Countries’ Medical Needs With strong economic growth, a combined population of nearly 2 billion people, and signi...
Cleanroom regulation – Find out what changes can we expect in ISO 146...
In this webinar you will learn: * How to stop using paper printouts for particle counting results while maintaining 21 CFR part 11 Compliance * How to mee...
$1,799.00
Latin America: Regulatory Compliance Requirements for Life Science Products...
Course Description This two-day comprehensive Course on Latin America Regulatory compliance requirements will cover topics ranging from pre-clinical and cli...
$1,799.00
Understanding and Implementing the Medical Device Directive
Most medical devices marketed in the European Union must follow the Medical Device Directive (MDD); IVD device and active implantable devices have other directi...
Pharmaceutical Hazard Categorization and Control
Xcelience is delighted to present a free webinar from their "Scentific Seminar Series." These webinars engage the pharmaceutical community about the challenges...
$479.00
Clear as Mud: Obtaining & Marketing your 510(K) with Today’s FDA
An interactive workshop to ensure you understand how to obtain a 510(k) in today's environment at FDA. Knowing how to get your application through FDA quickl...
The Ins and Outs of CTMS Data Migration
You are considering implementing a new clinical trial management system (CTMS), or maybe you have already made the decision. But you are wondering: What should ...
Oracle Clinical / Remote Data Capture Implementation Standards and Best Pra...
As your organization implements or upgrades to a newer version of Oracle Clinical (OC) and Remote Data Capture (RDC), there are many considerations to take into...
How to Migrate Drug Safety and Pharmacovigilance Data Cost-Effectively and ...
With the advancement of technology and the high cost of maintaining legacy safety and pharmacovigilance systems, organizations are forced to migrate to the late...
Open Source Technologies for Clinical Trials
Eric Morrie, Manager for Clinical Programming at Abbott Vascular, shares his expertise in open source systems for clinical trials Open source is becoming mor...
Implementing Adaptive Clinical Trials
With the ever rising cost and complexity of clinical trials, adaptive design is a promising solution highly regarded by both pharmaceutical companies and regula...
Navigating Pediatric Regulations in the United States and European Union
The FDA and EMA's requirement of pediatric plans for new active ingredients, dosage forms, dosing regimens or routes of administration has made a thorough under...
Success Strategies in Life Sciences Industry
The life sciences industry faces many challenges, such as patent protection, increasing cost of conducting research and development (R&D), drying of product...
Reducing the Barriers to the Conduct and Oversight of Clinical Trials: A Ca...
In a recent announcement of the proposed revisions to existing federal regulations governing human research subjects, the US Department of Health and Human Serv...
CDISC® SDTM Conversion
The mission of CDISC is to develop and support global, platform-independent data standards to improve medical research. As a CDISC Gold Member, Clinovo has been...
Medidata Rave® Custom Functions
Configuring a clinical EDC study in Medidata Rave is simple with good training. Study builders can easily configure eCRFs and review complex edit checks and der...
Implementing Adaptive Clinical Trials
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 Technologies for Clinical Trials
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...
CRO Governance Model for Emerging & Virtual Biopharma
Regulatory requirements have significantly lengthened and complicated clinical trials, resulting in an 11% annual rise in clinical testing expenses and delays i...
Searching the Scientific Literature More Effectively
With thousands of articles being published weekly, there is no shortage of available information relevant to ones research. But how do you sift through so much ...
Open Source Technologies for Clinical Trials
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...
CDISC® SDTM Conversion
The mission of CDISC is to develop and support global, platform-independent data standards to improve medical research. As a CDISC Gold Member, Clinovo has been...
Accelerate Your Research and Discovery
The information space in which life scientists work is growing in complexity and volume, especially with the technological advances of next generation sequencin...
$189.00
Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ...
Summary This Medical Device training will be discussing the newly-updated requirements of the Medical Device Directives, their linkage to the EU Clinical Trial...
$189.00
Drug Master Files (DMFs) – Understanding and Meeting Your Global Regu...
Description : This DMFs (Drug Master Files) training will discuss the current review and enforcement climate within FDA and the manner in which drug master file...
$.
Welcome to M and C Packaging India
We are attempting here to make you aware of the benefits that other organizations like yours have realized from working with M&C Packaging. It would be our ...
Implementing the Rave Custom Functions Best Suited to your Clinical Study R...
Configuring a clinical EDC study in Medidata Rave is simple with good training. Study builders can easily configure eCRFs and review complex edit checks and der...
CDISC Express Demo
Discover CDISC® Express, our free innovative SDTM mapping tool. CDISC Express is a free SAS application that automatically converts clinical data into CDISC S...
Open Source Technologies for Clinical Trials
Eric Morrie, Manager for Clinical Programming at Abbott Vascular, shares his expertise in open source systems for clinical trials Open source is becoming mor...
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