• Skip to content
  • Skip to footer

+358 20 7446 800

contactus@medfiles.eu

  • Suomi

Search

Extranet

LinkedIn Twitter YouTube

MedfilesMedfiles

Securing a healthier tomorrow

  • Home
  • About us
    • CEO’s greetings
    • Company Information
    • Values, Mission and Vision
    • Board
    • Executive board
    • History
    • Our clients
  • Our Services
    • Analytical services
    • Microbiological services
    • Product development and production of IMPs
    • Clinical study services
    • Regulatory affairs of human and veterinary medicines
    • Pharmaceutical documentation
    • Medical devices and IVDs
    • Food and nutrition services
    • QP, quality and distribution practices
    • Translation services
    • Health economics and market access services
    • Pharmacovigilance Services for Human and Veterinary Medicines
  • Contact us
    • Offices
    • Contact personnel
    • Contact form
  • Careers
  • News & Events
Home  News  Medfiles is proud to be a part of new CIOMS Working Group

Medfiles is proud to be a part of new CIOMS Working Group

30.11.2017

In November 2017, CIOMS launched a Working Group (WG) composed of key stakeholders including academia, regulators, public-private partnerships for product development and industry partners to address the present challenges and opportunities for clinical research in Resource Limited Settings (RLS). This WG aims to develop a consensus on relevant scientific issues and propose pragmatic recommendations for improvement of the environment and good practices for social acceptance, planning, assessing, performing and interpreting randomized controlled clinical trials in RLS. Furthermore, collaborative efforts aimed at capitalizing on existing initiatives/ documents will also be part of the WG in order to provide output that is as comprehensive as possible, does not duplicate other efforts and has added value. We are proud to be a part of this group as the only CRO member representing service providers’ field.

More information here.

Latest posts in News

  • The Finnish Medicines Agency Fimea Requires Swedish Summaries of Product Characteristics

    14.02.2019

  • Ready to go through Brexit?

    31.01.2019

  • Medfiles offers GMP-compliant bacterial endotoxin testing

    23.11.2018

Footer

  • R&D / Laboratory services
    • Analytical services
    • Microbiological services
    • Product development and production of IMPs
    • QP, quality and distribution practices
  • Clinical Study / Safety Services
    • Clinical study services
    • Medical devices and IVDs
    • Food and nutrition services
    • QP, quality and distribution practices
    • Pharmacovigilance Services for Human and Veterinary Medicines
  • Regulatory services
    • Regulatory affairs of human and veterinary medicines
    • Pharmaceutical documentation
    • Medical devices and IVDs
    • Food and nutrition services
    • QP, quality and distribution practices
    • Translation services
    • Health economics and market access services
    • Pharmacovigilance Services for Human and Veterinary Medicines

© Copyright Oy Medfiles Ltd. All rights reserved.
Volttikatu 5, FI-70700 Kuopio, FINLAND | Tel. +358 20 7446 800

LinkedIn Twitter YouTube