250514
Application Form
PMDA-ATC GMP Inspection Seminar 2025
(Confirm program here:
https://www.pmda.go.jp/english/symposia/0325.html
)
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Required Fields
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Required Fields
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Full name
The information you provide here will be used exactly as entered, including upper and lower case letters, for official documents such as certificates and the participants list. Please ensure accuracy.
ex) Taro PMDA [first, then family name]
If your full name exceeds 30 letters including spaces, please shorten to fit
within the 30 letters limit
.
Male / Female
Male
Female
Calling name (Short name)
Name you wish to be called during the seminar, especially during discussions.
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Job title
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Country
Algeria
Argentina
Armenia
Australia
Austria
Azerbaijan
Bahamas The
Bahrain
Bangladesh
Bhutan
Botswana
Brazil
Brunei Darussalam
Cabo Verde
Cambodia
Cameroon
Canada
Chile
China
Colombia
Cuba
Denmark
DR Congo
Ecuador
Egypt
El Salvador
Ethiopia
France
Georgia
Germany
Ghana
Grenada
Guinea
Guyana
Hong Kong
Iceland
India
Indonesia
Israel
Kazakhstan
Kenya
Lao PDR
Latvia
Libya
Lithuania
Luxembourg
Malawi
Malaysia
Maldives
Malta
Mexico
Moldova
Mongolia
Mozambique
Myanmar
Namibia
Nepal
Nigeria
Oman
Pakistan
Papua New Guinea
Paraguay
Peru
Philippines
Poland
Russia
Rwanda
Saudi Arabia
Sierra Leone
Singapore
Slovenia
Somalia
South Africa
South Korea
Sri Lanka
Sudan
Switzerland
Taiwan
Tanzania
Thailand
Timor Leste
Togo
Tunisia
Turkey
Uganda
UK
Ukraine
USA
Uzbekistan
Vietnam
Zambia
Zimbabwe
**Other
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Country/Region (other)
If you chose "Other" in the above, please write your country or region name here.
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Organization
AEC (Analytical Expertise Center -Azerbaijan)
AGES-MEA (Austrian Medicines and Medical Devices Agency)
ANARME( Autoridade Nacional Reguladora de Medicamento - Mozambique)
ANMAT (National Administration of Drugs Foods and Medical Devices -Argentina)
ANSM (Agence nationale de sécurité du médicament et des produits de santé_France)
ANVISA (Agência Nacional de Vigilância Sanitária -Brazil)
ARCSA (National Agency for Regulation Control And Health Surveillance -Ecuador)
BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte -Germany)
CDSCO (Central Drugs Standard Control Organization -India)
CECMED (Cuba Regulatory Agency of Drugs and Medical Devices -Cuba)
COFEPRIS (Comisión Federal para la Protección contra Riesgos Sanitarios -Mexico)
CPPS (Center for Pharmaceutical Products Safety - Uzbekistan)
Danish medicines Agency
DAV (Drug Administration of Vietnam)
DDA (Department of Drug Administration Ministry of Health and Population -Nepal)
DDF MoH (Department of Drugs and Food Ministry of Health -Cambodia)
DGDA (Directorate General of Drug Administration -Bangladesh)
DIGEMID (Dirección General de Medicamentos -Insumos y Drogas -Peru)
DINAVISA (DIRECCION NACIONAL DE VIGILANCIA SANITARIA)
DMDC (Department of Medical Device and Construction -Vietnam)
DNM (Dirección Nacional de Medicamentos -El Salvador)
DoH (Department of Health -Hong Kong)
DPM (Directorate of Pharmacy and Medicine -DR Congo)
DRA (Drug Regulatory Authority -Bhutan)
DRAP (Drug Regulatory Authority of Pakistan)
EDA (Egyptian Drug Authority -Egypt)
EFDA (Ethiopian Food and Drug Administration)
ERIS (Entidade Reguladora Independente da Saúde_Cabo Verde)
FDA Ghana (Food and Drugs Authority -Ghana)
FDA Myanmar (Food and Drug Administration -Myanmar)
FDA Philippines (Food and Drug Administration Philippines)
FDD MoH (Food and Drug Department Ministry of Health -Lao PDR)
Health Canada
HRH (Department of Human Resources for Health -Myanmar)
HSA (Health Sciences Authority -Singapore)
IMA (Icelandic Medicines Agency -Iceland)
Indonesian FDA (BPOM)
INVIMA (Instituto Nacional de Vigilancia de Medicamentos y Alimentos -Colombia)
IPC (Indian Pharmacopoeia Commission)
ISP (Instituto de Salud Pública -Chile)
JAZMP (Agency for Medicinal Products and Medicinal Devices -Slovenia)
KIDS (Korea Institute of Drug Safety and Risk Management)
Maldives FDA (Food and Drug Authority -Maldives)
MCA (Medicines Control Authority -Zimbabwe)
MDA (Medical Device Authority -Malaysia)
Medicine and medical devices regulatory agency (Mongolia)
MFDS (Ministry of Food and Drug Safety -South Korea)
MHRA (Medicines and Healthcare products Regulatory Agency -UK)
Ministry of Health Wellness and Religious Affairs and General Administration-Grenada
MMA (Malta Medicines Authority -Malta)
MMDA (Medicines and Medical Devices Agency -Moldova)
MoH Brunei Darussalam (Ministry of Health -Brunei Darussalam)
MoH Guinea (Ministry of Health - Guinea)
MoH Guyana (Ministry of Health- Guyana)
MoH Indonesia (Ministry of Health -Indonesia)
MoH Israel (Ministry of Health -Israel)
MoH Libya (Ministry of Health -Libya)
MoH Luxembourg (Ministry of Health -Luxembourg)
MoH Oman (Ministry of Health -Oman)
MoH Togo (Ministry of Health -Togo)
MoH Tunisia (Ministry of Health -Tunisia)
MoH Uzbekistan (Ministry of Health of the republic of Uzbekistan)
MoH Zambia (Ministry of Health -Zambia)
MoHHS (Federal Ministry of Health and Human Services -Somalia)
MoPH (Ministry of Public Health -Cameroon)
MRA (Medicines Regulatory Authority -Botswana)
MSPRH (Ministry of Health Population and Hospital Reform -Algeria)
NAFDAC (National Agency for Food and Drug Administration and Control -Nigeria)
National Drug Regulatory Agecy of the Republic of Armenia
NDA (National Drug Auhority -Uganda)
NDDA (National Center for Expertise of Medicines and Medical Devices -Kazakhstan)
NDoH (National Department of Health -Papua New Guinea)
NDPM (National Directorate of Pharmacy and Medicine_Timor Leste)
NHRA (National Health Regulatory Authority -Bahrain)
NMPA (National Medical Products Administration -China)
NMPB(National Medicines and Poisons Board-Sudan)
NMRA (National Medicines Regulatory Authority -Sri Lanka)
NMRC (Namibia Medicines Regulatory Council)
NPRA (National Pharmaceutical Regulatory Agency -Malaysia)
NRA (National Regulatory Authority - The Bahamas)
Pharmacy and Medicines Regulatory Authority - Malawi
Pharmacy Board of Sierra Leone-Ministry of Health - Sierra Leone
PPB (Pharmacy and Poisons Board -Kenya)
RAMPA (Regulation Agency for Medical and Pharmaceutical Activities of Georgia)
Roszdravnadzor (Federal Service for Supervision in Healthcare -Russia)
Rwanda FDA
SAHPRA (South African Health Products Regulatory Authority)
SAM (State Agency of Medicines -Latvia)
Saudi FDA (Saudi Food and Drug Authority -Saudi Arabia)
SECMOH (State Expert Center of the Ministry of Health -Ukraine)
SMCA (The State Medicines Control Agency -Lithuania)
Swissmedic
TFDA (Taiwan Food and Drug Administration)
TGA (Therapeutic Goods Administration -Australia)
Thai FDA (Food and Drug Administration -Thailand)
TMDA (Tanzania Medicines and Medical Devices Authority)
TMMDA (Turkish Medicines and Medical Devices Agency)
URPL (Urząd Rejestracji Produktów Leczniczych -Poland)
US FDA (Food and Drug Administration -USA)
ZFDA (Zanzibar Food and Drug Agency -Tanzania)
*Other
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Organization (other)
If you selected "Other" in the preceding section, kindly provide the name of the organization with which you are affiliated.
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Location of your office
Headquarters
Local office
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Department / Division
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Attendee e-mail address
This will be used for all communications from the Secretariat. Please ensure that it remains accessible while you are traveling overseas and in urgent situations.
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Attendee e-mail address (sub)
Please enter an alternative e-mail address for back up purpose.
Any other e-mail address (If necessary)
Additional e-mail addresses to which copies of communication with the Secretariat should be sent.
(e.g. your supervisor or admin support staff)
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Phone number (Office)
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Phone number (Mobile)
Phone number (Mobile in Japan)
Phone number available during the stay in Japan
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Name and title of Head of Organization 1) Name:
All seminar invitees will receive an official letter addressed to their affiliated organization’s Head.
For this purpose, type the full addressee name with title, (e.g. Dr FUJIWARA Yasuhiro).
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Name and title of Head of Organization 2) Title:
All seminar invitees will receive an official letter addressed to their affiliated organization’s Head.
For this purpose, type the addressee title.
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Your expertise field
Marketing Approval Assessment
Clinical Trial Assessment
GMP/Quality Assurance
Post-market safety
Other
Other expertise field
If you chose "Other" in the above, please describe the details of your field.
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Level of your expertise field
Beginner
Intermediate
Advanced
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Years of experience as a Regulator in the field
Please fill in years of experience as a regulator in the field.
years
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Experience on GMP inspection
How many times have you ever conducted on-site GMP inspections?
less than 5
5 to 10
11 to 20
more than 20
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Your current regulatory appointments
Describe your current regulatory appointment in as much detail as possible, within a 300 character limit (including letters, numbers, spaces and punctuation, not 300 words).
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Your expectations
What specific issue you want to address in your work and what aspect you expect to learn from the seminar.
Briefly describe within a 300 character limit. (including letters, numbers, spaces and punctuation, not 300 words)
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Declaration of application
1. Please download the format from the following link;
Signature form
2. Please print out the form and have both your signature and the signature of the head of organization on it.
3. Please upload the PDF file
→ link to
Signature instruction
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Travel arrangement by PMDA
PMDA may provide flight tickets and accommodation as long as the participant follows an itinerary arranged by PMDA. Do you accept PMDA arrangement?
Yes.
I don’t need PMDA arrangements. I or my organization will bear them.
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Passport
Do you have a valid passport?
Yes
No
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Surname
Please enter Surname (Family name) written in your passport
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Given name
Please enter Given name (First name) written in your passport
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Visa application (1)
Please check documents required for traveling to Japan:
⋅ Confirm details at:
https://www.mofa.go.jp/j_info/visit/visa/short/novisa.html
⋅ For official/diplomatic passport holders:
https://www.mofa.go.jp/ca/fna/page22e_000692.html
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Do you need PMDA assistance to provide
Visa
application documents?
Yes
No
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Visa application (2)
If
No
, please check your answer.
my country/region is not required Visa to enter Japan.
I will be using official/diplomatic passport.
I already have a multiple-entry Japan Visa.
of other reason
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of other reason comment
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Health condition
Can you participate in the seminar without any specific medical assistance during your stay in Japan?
Yes
No
If it is No, please enter a comment.
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Announcement from PMDA
PMDA would like to send announcements regarding PMDA international activities (e.g., PMDA-ATC seminars, PMDA Updates) to your email address.
Do you wish to receive announcements from PMDA?
Yes
No, I do not wish to receive these announcements.
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