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IRW is a Nordic full service CRO. We are currently established in local offices in Sweden, Denmark, Finland and Norway. The IRW team is dedicated and professional, with a wide range of academic competence and solid experience of clinical research, pharmacovigilance, data management and biostatistics, as well as of working with both global and small pharmaceutical and biotech companies. Being a local Nordic CRO, we can provide you with our knowledge on local requirements and networks.
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Keywords: pharmacovigilance, clinical trials, data management, biostatistics, CRO, SOP, phase, device, safety, stockholm
Company website: www.irwcro.com
Description:
IRW is a full-service Clinical Research Organization (CRO), founded in 1999. We are currently established in local offices in Sweden, Denmark, Finland and Norway.
The IRW team is dedicated and professional, with a wide range of academic competence and solid experience of pharmacovigilance, clinical research, data management and biostatistics, as well as of working with global pharmaceutical and biotech companies, and of interacting with the various regulatory authorities.
Being a local Nordic CRO, we can provide you with our wide ranging knowledge on local requirements and networks.
Assurance of quality:
Our work is carried out according to current regulations and guidelines, i.e. ICH-guidelines, local ethical and regulatory requirements and IRW or Customers SOPs. All our procedures are also subject to our in-house Quality Assurance.
Services:
We offer professional Clinical Trial Management, Data Management, Biostatistics and Pharmacovigilance services (pre and post authorisation) for Pharmaceutical, Biotechnology and Medical Device companies.
Clinical Trial Management
IRW offers phase I-IV pharmaceutical trial management, as well as all classes of medical device investigations, from single-centre to multi-national projects.
Data Management and biostatistics
Efficient data management speeds the clinical trial process and ensures excellent data collection accuracy and consistency. We can meet all of your clinical data management needs.
Our experienced team of biostatisticians provide trial design consultation, statistical methodology recommendations, programming expertise as well as the reporting accuracy necessary to deliver your trial efficiently and on time.
Pharmacovigilance
We offer a full-service pharmacovigilance solution. Our professional team can act as your safety department or as reinforcement to your extant pharmacovigilance team.
We can manage your project from start to finish or function as a fully-integrated part of your team.
Our staff is either outsourced or works with in-house projects.
Practical information:
For more information please contact us or visit our company website www.irwcro.com
Last updated: 2009-10-08
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A-Ö
Clinical trials
3H Biomedical
A+ Science
AAC Global
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