Reporting of adverse events ONLY

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:

+420 224 910 672

(from 09.00-17.30 CET)

+420 226 251 459

(non-stop 24/7)

To contact us about any other issue please call:

+420 22 491 0000or our regional offices.

Hlášení nežádoucích príhod

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:

+420 224 910 672

(09.00-17.30 CET)

+420 226 251 459

(non-stop 24/7)

Pro záležitosti, které se netýkaji farmakovigilance, kontaktujte prosím recepci:

+420 22 491 0000 nebo naše další pobočky.

ELC Group partners with mdi Europa GmbH to offer end-to-end regulatory solution for medical device companies in Europe

Preferred Partnership delivers complete consultancy support and expertise – from device registration to CE marking

Cambridge, UK, June 6 2012 – ELC GROUP, the pan-European pharmaceutical regulatory affairs organisation, today announces that it has formed a preferred European partner relationship with mdi Europa GmbH, a global regulatory consultancy for medical device and IVD companies. The two companies are partnering to provide a complete, end-to-end regulatory solution for medical device manufacturers in Europe – spanning initial device registration and documentation to CE marking and post-marketing services.

ELC Group has developed a strong track record and extensive expertise in medical device regulatory services, including regulation strategy, Medical Device Directive consultancy, device registration, and full technical file preparation. Through its Preferred Partnership arrangement with mdi Europa, ELC Group is now able to offer a one-stop, full-service consultancy solution to medical device manufacturers, focused on speeding time-to-market and easing the compliance process. With this new total service solution, ELC Group’s strengths in documentation support are complemented by mdi Europa’s skills in guiding companies to achieving CE certification and approvals, plus post-marketing device vigilance.

Commenting on today’s announcement, Marco Rubinstein, CEO of ELC Group said: “By joining hands with a regulatory organisation of the calibre of mdi Europa, we are offering our customers a true best-in-class solution for end-to-end medical device compliance. The breadth of this combined solution means that customers can benefit from a smoother regulatory process and faster time-to-market, all in the confidence that they are getting the very highest quality consultancy, support and advice available.”

mdi Europa Vice President Operations, Martina Sander-Giesemann, added: “It was most important for us to find a partner that has an equal understanding of customer service. With ELC Group, we have found an experienced, well-positioned partner that focuses on customer needs in the same way as we do. Regulatory compliance is often felt to be a burden – together with ELC Group, we do our utmost to take this burden off our mutual clients.”

ELC Group helps clients expedite time-to-market through a broad range of development capabilities, integrated advanced technologies, regulatory affairs consulting, and commercialisation services. ELC Group delivers its customised solutions through four core business segments: Regulatory Affairs Services; Medical Devices; EU REACH (Registration, Evaluation and Authorisation of Chemicals) Regulation Services; and Corporate Languages Solutions (Translations, Design, DTP, Localisation).