Scrip is part of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC’s registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction
UsernamePublicRestriction

Pharma Industry Finland elects board

This article was originally published in Scrip

Executive Summary

Pharma Industry Finland (PIF) has elected a new board. Ilpo Tolonen, managing director of MSD Finland became its new chairman, and Novartis Finland's MD Antti Viitanen and Orion Pharma's director Sari Kailanko were elected Mr Tolonen's first and second deputies respectively. Other board members are Leif Jokinen of H. Lundbeck, Jyrki Liljeroos of Santen, Jaakko Linna of Leiras Finland, Jyrki Lonnfors of AstraZeneca, Liisa Nuuros of Bayer, Harry Rastedt of GlaxoSmithKline, Ari Ronka of Ferring Laakkeet, Markku Santonen of Amgen and Ove Uljas of Pfizer. PIF's managing director, Suvi-Anne Siimes, was appointed the board secretary.

You may also be interested in...



Poland's new law fixes prices and trade mark-ups of reimbursed drugs

Poland's president, Bronislaw Komorowski, has signed a reimbursement bill into the law which will come into force on 1 January.

Global pharma boosts business in Russia - Why Russia (introduction)

In the past two years, most multinational pharmaceutical companies announced plans to create production facilities in Russia. They had been ignoring such an opportunity for years, and there were reasons for that. They included risks to investments, administrative barriers, unclear regulations assuming various interpretations and corruption.

Russia's president Medvedev wants talks on trials mutual recognition with US and EU

Russia's president Dmitriy Medvedev has requested that his government start talks with the US and the EU on the mutual recognition of clinical trial results (including paediatric trials) and prepare proposals for corresponding amendments of existing regulations.

Topics

Related Companies

UsernamePublicRestriction

Register

SC012001

Ask The Analyst

Please Note: Click here for more information on the Ask the Analyst service.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel