Email this pageEmail this pagePrint this pagePrint this page
Share on LinkedInShare on LinkedInShare on FacebookShare on FacebookTweet thisTweet this

Life Sciences

Categories

Minimize menuMaximize menu

Minimize menuMaximize menuHomeLife SciencesClinical Research ServicesEarly Phase I-IIaRegulatory & Pharmacovigilance

Related Services & Resources

Regulatory and Pharmacovigilance

SGS Regulatory and Pharmacovigilance Services provide vital support to organizations striving to meet international and regulatory standards as they progress from preclinical testing to clinical trials and beyond to post approval requirements.

With the combined skills and knowledge of 50 experienced, multilingual specialists with global experience in regulatory submissions and drug safety programs, our team applies its expertise internationally and locally, facilitating the submissions process for the pharmaceutical and biotechnology industries. We draw on the knowledge we have gained from our our close work with regulatory agencies worldwide, including the EMEA and local country health authorities, and we ensure that all of our experts are trained to meet the requirements of the International Conference on Harmonization (ICH), EMEA/CPMP, the FDA and other important regulatory bodies.

As a world leader in Life Science Services, we have over 35 years’ experience as a global contract organization, and we are able to shape our clinical research regulatory compliance services to meet the diverse needs of our clients, from those working on single compounds to  those leading a full drug development program.

Whatever your particular requirements, you can choose from a comprehensive range of clinical research regulatory and drug safety compliance services:

  • Regulatory intelligence – keeping you up to date with regulatory requirements and how to meet them
  • Submission support – providing country-specific submission packages and tracking
  • Medical monitoring – including access to medical review and 24/7 support
  • Drug safety case management support – wide-ranging help with specific drug development safety  monitoring and plans
  • Report writing – to demonstrate the safety of your products
  • Setting up and organizing Data Safety Monitoring Boards
  • Setting up safety databases

Whatever clinical trial submissions or marketing application you are working to complete, SGS can help make them seem less daunting. We always work to the high standard our name has come to be associated with, and every client receives the same levels of integrity and flexibility.

Email Us

Contact

SGS Headquarters

  • 1 Place des Alpes
  • P.O. Box 2152
  • Geneva, 1211
  • Switzerland
  • t   +41 22 739 91 11
  • f   +41 22 739 98 86
  • e   Email Us

E-SUBSCRIPTIONS

Sign up to SGS publications and newsletters from your region and around the world
STAY UP TO DATE.SUBSCRIBE NOW

Office Directory

Find SGS offices and labs around the world.World map
Office Locator

News

events