Patients should always seek the advice of a doctor or pharmacist in case of adverse events.
If you wish to report an adverse event to ELC Group s.r.o., please find the contact information below:
To contact us about any other issue please call:
Pacienti by meli vždy požádat o radu svého lékare nebo lékárníka v prípade výskytu nežádoucích príhod.
Pokud chcete nahlásit nežádoucí príhodu spolecnosti ELC Group s r.o., prosím využijte kontaktních údaju níže:
Pro záležitosti, které se netýkaji farmakovigilance, kontaktujte prosím recepci:
+420 22 491 0000 nebo naše další pobočky.
Dr. Parvinder Punia, Senior regulatory expert will present “European experience of harmonising the pharmaceutical market” at Moscow conference on February 10th 2015
Cambridge, UK, 2nd February, 2015 – ELC Group, one of the fastest-growing providers of regulatory affairs, today announces that its Senior Regulatory Affairs Manager Dr Parvinder Punia will be an invited speaker at the 3rd Annual Regulatory & Legal Affairs in Russia conference being held at the Marriott Grand Hotel in Moscow from February 10th – 12th 2015.
Dr. Punia will be speaking on the opening day of the conference, Tuesday 10th February in the afternoon, on the topic of “European experience of harmonising the pharmaceutical market”, which forms part of the special Focus Day “Circulation of drugs within the customs Union and Eurasian Economic Union”. Dr. Punia was invited to give the keynote presentation due to the Russia and CIS program of harmonisation now taking place, and to provide authoritative insight on the lessons learned from the EU, both positive and negative. Last year, ELC Group announced the opening of a regional base in Russia following a year of record growth, and the appointment of Inna Demidova as a Senior Regulatory Affairs Expert for Russia and the Commonwealth of Independent States (CIS).
Regulatory & Legal Affairs in Russia 2015 is a three-day conference attended by more than 150 industry professionals, including government representatives, international specialists, leading physicians and pharmaceutical associations. The pre-conference focus days and main two-day conference will be addressed by more than 50 expert speakers from across pharmaceutical regulatory spectrum.
With a scientific background, Dr. Punia has nine years’ regulatory experience, which includes 3 years from within two EU Health Agencies (Portugal and MHRA in the UK). She has represented the UK agency at the EMEA level. Her key expertise is in strategy, budgeting, preparation, co-ordination and review of a variety of scientific and regulatory documents for European and experience in non-European countries. Dr. Punia has an extensive knowledge of the development cycle and internal knowledge of the EU and other regulated region procedures and has worked in a business development capacity.
For more information about the conference and to register to attend, please visit: http://www.pharma-regulatory-affairs.com/
