QUALITY, A PILLAR ON WHICH TO EXPERIENCE EXCELLENCE
For the entire production cycle, starting from the Active Pharmaceutic ingredients to the finished products, we ensure quality, efficacy and safety.
Our Quality System is managed by a dedicated Unit, structured in a Quality Assurance Unit and a Quality Control Unit, consisting of laboratories for physical and microbiological chemical controls.
electronic batch record
A highly computerized Quality Management System that guarantees the achievement of the quality objectives, increasing the degree of effectiveness and efficiency.
Our Certification
quality, environment and safety certifications
medical device certification
drug’s safety
We aim to continuously evaluate all the information related to the drug’s safety. We ensure for all the marketed drugs a favorable risk-benefit ratio.
For any report of an adverse event, please fill out the form below to send us your report.
drug’s safety
Pharmacovigilance is an essential phase in the development and use of a drug.
It aims to collect and evaluate, on an ongoing basis, information on drug response, including suspected adverse reactions.
Pharmacovigilance through continuous monitoring has the task of keeping under constant control the risk / benefit of drugs available on the market, making sure that the latter is always in favor of the patient’s health.
PHARMACOVIGILANCE REPORTING FOR THE PATIENT
For reports of suspected adverse reactions, kind patients are invited to contact their doctor.
Communications must be made using a special form that can be downloaded from the website of the Italian Medicines Agency (AIFA)
PHARMACOVIGILANCE REPORTING FOR DOCTORS AND HEALTHCARE OPERATORS
Si invitano i signori Medici a seguire quanto previsto dall’Agenzia Italiana del Farmaco:
PHARMACOVIGILANCE REPORTING FOR HEALTHCARE PROFESSIONALS AND PATIENTS
Alternatively, the link is indicated through which it is possible to report, directly online, a suspected adverse reaction.
If you wish to contact the pharmacovigilance service of DAMOR FARMACEUTICI directly, you can contact:
Dr. Viola Di Marco
Download the information:
INFORMATION FOR HEALTHCARE OPERATORS
INFORMATION FOR PATIENTS
the medical device vigilance
It has the objective of collecting and evaluating, on an ongoing basis, information on the safety of the devices, including suspected adverse reactions.
If you wish to contact the medical device vigilance service of DAMOR FARMACEUTICI directly, you can contact:
Dr.ssa Gabriella Cannavale
ethicalCode
Rules and guidelines
for the activity and the action of the collaborators
in view of the common goals.
Interactions with Health Care Professionals
METHODOLOGICAL NOTE
YEAR 2019
YEAR 2020
Farmaceutici Damor Spa is the assignee of the Research Projects with the contribution of:
The Research Project nr: CdS00463_CUP C61B19000160008 of Farmaceutici Damor Spa focuses mainly on
“Development and testing of medical devices for the treatment of acute and chronic topical lesions”.
“Public funding disclosure requirements: State aids and De Minimis aids received by this company are published in the National Register of State Aids, pursuant to art. 52 of Law 234/2012, and can be consulted, by entering as search key in the field “FISCAL CODE” our fiscal code”.