At DRL, we strive to ensure the highest level of quality, safety, and efficacy of our products to deliver consistent and intended results. Through robust monitoring systems and quality assurance, we produce safe healthcare products through our state of the art, automated machinery and qualified personnel.
DYSON’s Pharmacovigilance Program monitors, categorizes, assesses and evaluates any possible Adverse Drug Reactions (ADR’s) that may have been caused by its marketed products.
All Adverse Drug Reactions (ADR’s) should be reported immediately/within 24 hours to firstname.lastname@example.org
If you have purchased or received a DYSON product that is damaged, defective or not in its defined specifications, please download and complete this form, and return it to email@example.com.