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Evènement :3rd European Clinical Trials Inspection Readiness Summit

Dates :Lundi 22 Mai 2017 - Mardi 23 Mai 2017

Lieu :Radisson Blu Edwardian Heathrow Hotel
140 Bath Rd
UB3 5AW Harlington, Hayes, Royaume-Uni

Type :Conférence & Séminaire - Audience Internationale

Accréditation :--


 

Informations

 

An inspection from the FDA can pop up at any time throughout a clinical trial pipeline, and being prepared is key. The industry must move toward innovative methods and utilize new technologies to ensure compliance in a global environment. Change your inspection readiness strategy into one that is proactive and preventative, instead of one that is mainly concerned with putting out fires. Developing effective strategies for risk management through careful vendor selection and oversight, expert knowledge of FDA guidances, budget management, and TMF and pharmacovigilance audits will put your organization ahead of the pack.
 
The 3rd European Clinical Trials Inspection Readiness Summit is designed to explore best practices for developing and maintaining compliance at clinical trial inspection sites. Delegates will leave the event armed with strategies regarding partner oversight, metrics, data quality, TMFs and risk assessment tools. Additionally, this event will provide opportunities for sharing best practices and networking across all contributors and stakeholders, including sponsors, regulators, CROs and project teams.
 
Top 5 Reasons to Attend for 2017:
1. Review crucial information and analyze regulations from around the world, with a focus on FDA, EMA, PMDA and MHRA regulations
2.Benchmark the success of your clinical trial using metrics that measure the performance of CROs and trial sites
3. Learn strategies for ensuring there is a comprehensive clinical trial storyboard so inspectors can recreate the trial
4. Leverage process maps that can be applied to streamline TMF management and the key team members who need to be involved
5. Innovate your inspection readiness SOPs to arm them with information on risk-based modeling for inspection readiness
 
Time: 8:00 am - 5:00 pm
 
Prices:
 
Early Bird Rate: (Register By April 14, 2017): GBP 1450
Standard Pricing: (Register by May 21, 2017): GBP 1550
Onsite Pricing: GBP 1650
 
URLs:
 
Website: https://go.evvnt.com/107698-0
Booking: https://go.evvnt.com/107698-1
Brochure: https://go.evvnt.com/107698-2
 
Speakers: Michele Weitz, Pramod Wable, Nina Beck Toubro, Geoff Taylor, Birthe Emilie Neilsen, Kathleen Meely, Karen Edelmann-Stergiou, Celia Gibson, Franck Gressier, Karen Hue, Maria Nymann Jensen

 

Lieu

Plan et itinéraire
Adresse de la conférence :
Radisson Blu Edwardian Heathrow Hotel
140 Bath Rd
UB3 5AW Harlington, Hayes
Royaume-Uni
Plan et itinéraire

Renseignements

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Précisions

3rd European Clinical Trials Inspection Readiness Summit Pharmacie
quality assurance, inspection readiness, clinical trials, clinical operations, clinical research, clinical, clinical trial, data management
Tout public
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English

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