A
A
A
Home
Organisation
About Us
Mission and Objectives
Directorates and Units
Committees and Working Groups
Annual Reports
Heads of Medicines Agencies
Working at the Malta Medicines Authority
Career Opportunities
Bank and Payment Details
Data and Information
Freedom of Information
Data Protection
Presentations and Publications
Links
Medical Devices
Pharmacy Roster
eHealth
Government of Malta
Heads of Medicines Agency
Innovative Medicines Initiative
European Medicines Agency
Legislation
Introduction
Better Regulation
Legislation Documentation
Medicines Act
Medical Device Legislation
EU Legislation
Consultation
Collaboration
Request for Collaborative Agreements
EU & Medicines Authority Consultations
EU & Medicines Authority Consultations
News & Events
News
Press Releases
Circulars
Other News
Past News
Events
Latest Events
Past Events
Online Services
Online Services
Eudrapharm
EU Common Submission Portal
Medicines Authority Notifications
Servizz.gov.mt
Online Applications (E-Forms)
Newsletters
Contact and Connect
On Line Forms
Enquiries and Feedback
Complaints
Complaints related to Advertising of Medicinal Products
Report Product Defect
Report a Side Effect - Adverse Drug Reaction (ADR)
Connect and Share
Engage with us on Facebook
Follow us on LinkedIn
Follow us on Twitter
Connect with us on Google
Watch our videos on YouTube
Find Us
Contact Details
Previous
Next
Patient / Consumer
Know more about Medicines Regulation
Know more about access to medicines which do not have a Marketing Authorisation
Report a Side Effect
Biological and Biosimilar Medicinal Products
How we monitor the safety of medicines
Know more about the Medicines Supply Chain
Know more about Use of Medicines
Information Leaflets on Medicines
Search for your Medicines
Industry
Pharmaceutical Activities and Inspections
Product Quality Defects Reporting
Scientific Advice
Advertising
Registering a product
Pharmacovigilance
Fees
Health Care Professionals
Search Authorised Medicines in Malta
Adverse Drug Reaction Reporting
How we monitor the safety of medicinal products
Safety Information
Clinical Trials
Product Quality Defects Reporting
Medicines supply chain and regulation
Advertising
Home
/
Contact and Connect
/
On line Request for Forms
/ Enquiries
Enquiries
Useful Links
Medical Devices
Pharmacy Roster
eHealth
Government of Malta
Heads of Medicines Agency
Innovative Medicines Initiative
European Medicines Agency
Activities
Pharmaceutical Activities and Inspections
Scientific Advice
Recalls and Rapid Alerts
Registration of Medicinal Products
Advertising
Borderline Products
Changes to prescription status
Safety Recalls
BREXIT - Regulatory considerations
Advanced Scientific Initiatives
Cannabis for Medicinal and Research Purposes
Linguistic Checks
Safety
Clinical Trials
Enforcement and Market Surveillance
Malta Medicines Authority
Sir Temi Zammit Buildings,
Malta Life Sciences Park,
San Gwann SGN 3000
Malta
Email
: info.medicinesauthority@gov.mt
Telephone
: 356 2343 9000
Helpline
: 356 2343 9100
Fax
: 356 2343 9161
View Large Map
Maldives
Mauritius
Morocco
Norway
Afghanistan
Albania
Algeria
American Samoa
Andorra
Angola
Anguilla
Antarctica
Antigua and Barbuda
Argentina
Armenia
Aruba
Australia
Austria
Azerbaijan
Bahamas
Bahrain
Bangladesh
Barbados
Belarus
Belgium
Belize
Benin
Bermuda
Bhutan
Bolivia
Bosnia Herzegovina
Botswana
Bouvet Island
Brazil
British Indian Ocean Territory
British Virgin Islands
Brunei
Bulgaria
Burkina Faso
Burundi
Cambodia
Cameroon
Canada
Cape Verde
Cayman Islands
Central African Republic
Chad
Chile
China
Christmas Island
Cocos Islands
Colombia
Comoros
Congo
Cook Islands
Costa Rica
Croatia
Cuba
Cyprus
Czech Republic
Denmark
Djibouti
Dominica
Dominican Republic
East Timor
Ecuador
Federated States of Egypt
El Salvador
Equatorial Guinea
Eritrea
Estonia
Ethiopia
New Caledonia
Falkland Islands
Faroe Islands
Fiji
Finland
France
French Guiana
French Polynesia
French Southern Territories
Gabon
Gambia
Georgia
Germany
Ghana
Gibraltar
Greece
Greenland
Grenada
Guadeloupe
Guam
Guatemala
Guinea
Guinea-Bissau
Guyana
Haiti
Heard and McDonald Islands
Honduras
Hong Kong
Hungary
Iceland
India
Indonesia
Iran
Iraq
Ireland
Israel
Italy
Ivory Coast
Jamaica
Japan
Jordan
Kazakhstan
Kenya
Kiribati
Korea
Kyrgyzstan
Laos
Latvia
Lebanon
Lesotho
Liberia
Libya
Liechtenstein
Lithuania
Luxembourg
Macau
Macedonia
Madagascar
Malawi
Malaysia
Mali
Malta
Marshall Islands
Martinique
Mauritania
Mayotte
Mexico
Micronesia
Moldova
Monaco
Mongolia
Montenegro
Montserrat
Mozambique
Myanmar
Namibia
Nauru
Nepal
Netherlands
Netherlands Antilles
New Zealand
Nicaragua
Niger
Nigeria
Niue
Norfolk Island
North
Northern Mariana Islands
Oman
Other
Pakistan
Palau
Panama
Papua New Guinea
Paraguay
Peru
Philippines
Pitcairn Island
Poland
Portugal
Puerto Rico
Qatar
Reunion
Romania
Russia
Rwanda
S. Georgia and S. Sandwich Isls.
Saint Kitts & Nevis
Saint Lucia
Saint Vincent and The Grenadines
Samoa
San Marino
Sao Tome and Principe
Saudi Arabia
Senegal
Serbia
Seychelles
Sierra Leone
Singapore
Slovakia
Slovenia
Somalia
South Africa
South Kuwait
Spain
Sri Lanka
St. Helena
St. Pierre and Miquelon
Sudan
Suriname
Svalbard and Jan Mayen Islands
Swaziland
Sweden
Switzerland
Syria
Taiwan
Tajikistan
Tanzania
Thailand
Togo
Tokelau
Tonga
Trinidad and Tobago
Tunisia
Turkey
Turkmenistan
Turks and Caicos Islands
Tuvalu
U.S. Minor Outlying Islands
Uganda
Ukraine
United Arab Emirates
United Kingdom
United States of America
Uruguay
Uzbekistan
Vanuatu
Vatican City
Venezuela
Vietnam
Virgin Islands
Wallis and Futuna Islands
Western Sahara
Yemen
Zaire
Zambia
Zimbabwe
NOT APPLICABLE
Licensing (incl variations, renewals, notifications and transfers)
Pharmacovigilance
Inspectorate and Enforcement
Other
I have accepted the
Terms and Conditions