Sunday, March 31, 2013

Searching for similar research, reviewers and journals


When writing a paper and a proposal, it is crucial to identify relevant research; and before submitting an article, a good search for potential reviewers and related journals is required.
Some time ago I found out that web servers can help authors with such process. I am actually using EtBlast, you might also find it helpful.

If you have other suggestions, please share! 

link for EtBlast:       http://etest.vbi.vt.edu/etblast3/

Dancing your PhD?

For the Doctoral students: Have you ever thought of dancing your PhD?!

have a look at the link below, might prove inspiring!

http://news.sciencemag.org/sciencenow/2012/10/dance-your-phd-and-the-winner-is.html

Vacancies

For the ones interested in vacancies...
don't forget to check out the Job Board of the ISOQoL site!

http://jobs.isoqol.org/home/home.cfm?site_id=14874

There are some open vacancies at the moment!

Friday, March 22, 2013

One-day course on PROs in London, June 13, 2013

For those in Europe, there is a one-day course being offered by Oxford Outcomes and ICON about the development of PROs

PATIENT REPORTED OUTCOMES 2013: DEVELOPMENT AND APPLICATION
13th June, 2013
Time: 08:30 - 17:30
Location: Sofitel Hotel, Heathrow, London
Timezone: (GMT) Western Europe Time, London, Lisbon, Casablanca
A new 1-day course offered to those with an interest in the construction and use of patient reported outcomes (PROs) in the development, assessment and reimbursement of medicines. This is an intermediate course suitable for novices and experienced participants alike, and will have relevance to international participants from academia, health care providers, as well as the pharmaceutical, regulatory and device development industries.

Course objectives
  • Understand the scope and range of PRO measurement and ascertain how PROs support medicine and device development and approval in the EU and US.
  • Understand the key considerations when selecting a PRO for a particular use and be able to evaluate a PRO accordingly.
  • Develop an understanding of the steps required to develop and validate a PRO, and ensure translatability in additional language and electronic formats.
  • Gain awareness of regulatory requirements from EMA/ FDA, the needs of NICE regarding PROs and the use of PRO data by other decision makers.
You can read more here: 
http://www.iconplc.com/news-events/events/workshops/patient-reported-outcomes/index.xml