Our broad range of safety
services covers every
stage of a product’s
Med-ERRS is dedicated to serving the
pharmaceutical industry around the world to ensure
medication safety during the naming, packaging,
label design and evaluation process. Throughout the
United States, Europe, Canada, Asia and South
America, we provide services that span a product’s
lifecycle, from pre-marketing assessments at an
early phase of development through post-marketing
evaluations and line extensions.
PRODUCT DEVELOPMENT TIMELINE:
Failure Mode and Effects Analysis (FMEA)
, Med-ERRS helps companies determine the
likelihood that a proposed product, trademark, package label, package design, or technology
system would be vulnerable to user error.
In order to provide the widest breadth of safety services, we often collaborate with other companies including name creation companies, market research companies, human factors engineering companies and law firms. These companies help complement the services we offer by providing another area of expertise beyond safety to the project. We are happy to recommend our colleagues for you to work with directly, or we can coordinate with them as your primary client contact, depending on your needs.
If you are a company who provides services to the pharmaceutical and healthcare industry who would like to collaborate with Med-ERRS, please contact us.