Data Administration Updates: Ennov InSight 7.1.1.15

Running the migration script updates Data Administration with latest changes. The changes must be reviewed, and updated, as necessary.

EU v3.1 Updates

Country Code Country Name Health Authority Name Health Authority Abbreviation Health Authority eCTD Code Health Authority Website
AT Austria Austrian Federal Office for Safety in Health Care / Austrian Medicines and Medical Devices Agency BASG AT-BASG www.basg.gv.at
BE Belgium Federal agency for medicines and health products FAMHP BE-FAMHP http://www.fagg-afmps.be/
HR Croatia Agency for Medicinal Products and Medical Devices of Croatia HALMED HR-HALMED http://www.halmed.hr/
CY Cyprus Pharmaceutical Services - Ministry of Health PHS CY-PHS http://www.moh.gov.cy/
CZ Czech Republic State Institute for Drug Control SUKL CZ-SUKL www.sukl.eu
DK Denmark Danish Medicines Agency DKMA DK-DKMA www.lmst.dk
EE Estonia State Agency of Medicines SAM EE-SAM ravimiregister.ravimiamet.ee/en/default.aspx
FR France National Agency for the Safety of Medicines and Health Products ANSM FR-ANSM http://ansm.sante.fr/
DE Germany BfArM - Federal Institute for Drugs and Medical Devices BfArM DE-BFARM http://www.bfarm.de/
GR Greece Greek National Organization for Medicines EOF EL-EOF http://www.eof.gr/
HU Hungary National Institute of Pharmacy and Nutrition OGYI HU-OGYI www.ogyei.gov.hu
IS Iceland Icelandic Medicines Agency IMCA IS-IMCA http://www.ima.is/
IE Ireland The Health Products Regulatory Authority HPRA IE-HPRA http://www.hpra.ie
IT Italy Italian Medicines Agency AIFA IT-AIFA www.aifa.gov.it
LV Latvia State Agency of Medicines ZVA LV-ZVA http://www.zva.gov.lv
LI Liechtenstein Office of Health / Medicinal Products Control Agency LLV LI-LLV http://www.llv.li/
LT Lithuania State Medicines Control Agency SMCA LT-SMCA http://www.vvkt.lt/
LU Luxembourg Ministry of Health MINSANT LU-MINSANT www.ms.etat.lu
MT Malta Medicines Authority MRU MT-MEDAUTH http://www.medicinesauthority.gov.mt/
NL Netherlands Medicines Evaluation Board MEB NL-MEB http://www.cbg-meb.nl/
NO Norway Norwegian Medical Products Agency NOMA NO-NOMA https://www.dmp.no/
PL Poland Office for Registration of Medicinal Products, Medical Devices and Biocidal Products URPL PL-URPL http://www.urpl.gov.pl/
PT Portugal National Authority of Medicines and Health Products, IP INFARMED PT-INFARMED http://www.infarmed.pt/
SK Slovakia State Institute for Drug Control SIDC SK-SIDC http://www.sukl.sk/
SI Slovenia Agency for Medicinal Products and Medical Devices of the Republic of Slovenia JAZMP SI-JAZMP http://www.jazmp.si/
ES Spain Spanish Agency for Medicines and Health Products AEMPS ES-AEMPS http://www.aemps.gob.es/
SE Sweden Medical Products Agency MPA SE-MPA http://www.lakemedelsverket.se/

Assembly - Assembly DTD/Schema Type

If the 'EU-3-1' Assembly DTD/Schema type already exists in the Assembly - Assembly DTD/Schema Types section in Data Administration, it will be activated (if inactive) and updated to have the code value 'EU-3-1'. Otherwise, the 'EU-3-1' Assembly DTD/Schema will be added.

Sequence Maintenance - Filing Type Values

Filing Type values will be added to the Sequence Maintenance – Filing Type values section in Data Administration, if they do not already exist. The list of new values can be found in the table below:

Filing Type Display Name Countries
Article 18 Filing Article 18 Filing Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, European Union, Finland, France, Germany, Great Britain, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Liechtenstein, Lithuania, Luxembourg, Malta, Netherlands, Northern Ireland, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Undefined, United Kingdom

Submission Maintenance - Sub Filing Type Values

Sub Filing Type values will be added to the Submission Maintenance – Sub Filing Type values section in Data Administration, if they do not already exist. The list of new values can be found in the table below:

Sub Filing Type Countries
Initial Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, European Union, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Liechtenstein, Lithuania, Luxembourg, Malta, Netherlands, Northern Ireland, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, South Africa, Spain, Sweden, Undefined, United Kingdom
Closing Information Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, European Union, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Liechtenstein, Lithuania, Luxembourg, Malta, Netherlands, Northern Ireland, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, South Africa, Spain, Sweden, Undefined, United Kingdom
Validation Response Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, European Union, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Liechtenstein, Lithuania, Luxembourg, Malta, Netherlands, Northern Ireland, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Undefined, United Kingdom
Response Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, European Union, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Liechtenstein, Lithuania, Luxembourg, Malta, Netherlands, Northern Ireland, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Undefined, United Kingdom
Additional Information Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, European Union, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Liechtenstein, Lithuania, Luxembourg, Malta, Netherlands, Northern Ireland, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Undefined, United Kingdom
Consolidating Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, European Union, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Liechtenstein, Lithuania, Luxembourg, Malta, Netherlands, Northern Ireland, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Undefined, United Kingdom
Corrigendum Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, European Union, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Liechtenstein, Lithuania, Luxembourg, Malta, Netherlands, Northern Ireland, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Undefined, United Kingdom
Reformat Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, European Union, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Liechtenstein, Lithuania, Luxembourg, Malta, Netherlands, Northern Ireland, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Undefined, United Kingdom
Re-examination Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, European Union, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Liechtenstein, Lithuania, Luxembourg, Malta, Netherlands, Northern Ireland, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Undefined, United Kingdom

Submission Maintenance - Filing Type eCTD Codes

The Filing Type eCTD Codes values will be added to the Submission Maintenance > Filling Type Values section in Data Administration if they do not already exist. If they exist, the eCTD Code for eu-3-1 DTD/Schema is added to them. The list of new values includes the following:

Filing Type (Display Name) Applicable DTD/Schema eCTD Code Available for Filing Type
Marketing Authorisation Application eu-3-1 maa MAA, MAA-AH
Variation 1A Filing eu-3-1 var-type1a MAA, MAA-AH
Variation 1AIN Filing eu-3-1 var-type1ain MAA, MAA-AH
Variation 1B Filing eu-3-1 var-type1b MAA, MAA-AH
Variation 2 Filing eu-3-1 var-type2 MAA, MAA-AH
National Variation Filing eu-3-1 var-nat MAA, MAA-AH
Extension Filing eu-3-1 extension MAA, MAA-AH
Repeat Use Procedure eu-3-1 rup MAA, MAA-AH
Periodic Safety Update Report eu-3-1 psur MAA, MAA-AH
PSUR single assessment procedure eu-3-1 psusa MAA, MAA-AH
Risk Management Plan Filing eu-3-1 rmp MAA, MAA-AH
Renewal Filing eu-3-1 renewal MAA, MAA-AH
Specific Obligation Related to PAM eu-3-1 pam-sob MAA, MAA-AH
Annex II Condition Related to PAM eu-3-1 pam-anx MAA, MAA-AH
Additional PV Activity in the RMP Related to PAM eu-3-1 pam-mea MAA, MAA-AH
Legally Binding Measure Related to PAM eu-3-1 pam-leg MAA, MAA-AH
SDA Submission Related to PAM eu-3-1 pam-sda MAA, MAA-AH
Corrective/Preventive Action Related to PAM eu-3-1 pam-capa MAA, MAA-AH
Paediatric Submission Related to PAM (Article 45) eu-3-1 pam-p45 MAA, MAA-AH
Paediatric Submission Related to PAM (Article 46) eu-3-1 pam-p46 MAA, MAA-AH
PAES Submission Related to PAM eu-3-1 pam-paes MAA, MAA-AH
Recommendation Related to PAM eu-3-1 pam-rec MAA, MAA-AH
PASS Protocol Submission (Article 107n) eu-3-1 pass107n MAA, MAA-AH
PASS Report Submission (Article 107q) eu-3-1 pass107q MAA, MAA-AH
ASMF Filing eu-3-1 asmf MAA, MAA-AH
Plasma Master File eu-3-1 pmf MAA, MAA-AH
Article 20 Referral eu-3-1 referral-20 MAA, MAA-AH
Article 29(4) Referral eu-3-1 referral-294 MAA, MAA-AH
Article 29 Paediatric Referral eu-3-1 referral-29p MAA, MAA-AH
Article 30 Referral eu-3-1 referral-30 MAA, MAA-AH
Article 31 Referral eu-3-1 referral-31 MAA, MAA-AH
Article 35 Referral eu-3-1 referral-35 MAA, MAA-AH
Article 5(3) Referral eu-3-1 referral-5-3 MAA, MAA-AH
Article 107i Referral eu-3-1 referral-107i MAA, MAA-AH
Article 16c (1c)i Referral eu-3-1 referral-16c1c MAA, MAA-AH
Article 16c(4) Referral eu-3-1 referral-16c4 MAA, MAA-AH
Annual Reassessment Filing eu-3-1 annual-reassessment MAA, MAA-AH
USR Filing eu-3-1 usr MAA, MAA-AH
Clinical Data for Publication – Redacted Proposal eu-3-1 clin-data-pub-rp MAA, MAA-AH
Clinical Data for Publication – Final Version eu-3-1 clin-data-pub-fv MAA, MAA-AH
PAED Related to PIP (Article 7, 8, 30) eu-3-1 paed-7-8-30 MAA, MAA-AH
PAED Article 29 Filing eu-3-1 paed-29 MAA, MAA-AH
PAED Article 45 eu-3-1 paed-45 MAA, MAA-AH
PAED Article 46 eu-3-1 paed-46 MAA, MAA-AH
Article 58 Filing eu-3-1 article-58 MAA, MAA-AH
Notification 61-3 Filing eu-3-1 notification-61-3 MAA, MAA-AH
Transfer MA Filing eu-3-1 transfer-ma MAA, MAA-AH
Lifting Suspension Filing eu-3-1 lifting-suspension MAA, MAA-AH
Withdrawal Filing eu-3-1 withdrawal MAA, MAA-AH
CEP Submission eu-3-1 cep MAA, MAA-AH
None eu-3-1 none MAA, MAA-AH
Article 18 Filing eu-3-1 article-18 MAA, MAA-AH

Submission Maintenance - Sub Filing Type eCTD Codes Values

Sub Filing Type eCTD codes values will be added to the Submission Maintenance – Sub Filing Type values section in Data Administration, if they do not already exist. If they already exist, the eCTD Code for ZA-3-0 DTD/Schema is added to the value. The list of new values can be found in the table below:

Sub Filing Type (Display Name) Applicable DTD/Schema eCTD Code Available for Filing Type
Initial eu-3-1 initial Marketing Authorisation Application,Variation 1A Filing,Variation 1AIN Filing, Variation 1B Filing, Variation 2 Filing, National Variation Filing, Extension Filing, Repeat Use Procedure, Periodic Safety Update Report, PSUR single assessment procedure, Risk Management Plan Filing, Renewal Filing, Specific Obligation, Related to PAM, Annex II Condition Related to PAM, Additional PV Activity in the RMP Related to PAM, Legally Binding Measure Related to PAM, SDA Submission Related to PAM, Corrective/Preventive Action Related to PAM, Paediatric Submission Related to PAM (Article 45), Paediatric Submission Related to PAM (Article 46), PAES Submission Related to PAM, Recommendation Related to PAM, PASS Protocol Submission (Article 107n), PASS Report Submission (Article 107q), ASMF Filing, Plasma Master File, Article 20 Referral, Article 29(4) Referral, Article 29 Paediatric Referral, Article 30 Referral, Article 31 Referral, Article 35 Referral, Article 5(3) Referral, Article 107i Referral, Article 16c (1c)i Referral, Article 16c(4) Referral, Annual Reassessment Filing, USR Filing, Clinical Data for Publication - Redacted Proposal, Clinical Data for Publication - Final Version, PAED Related to PIP (Article 7, 8, 30), PAED Article 29 Filing, PAED Article 45, PAED Article 46, Article 58 Filing, Notification 61-3 Filing, Transfer MA Filing, Lifting Suspension Filing, Withdrawal Filing, CEP Submission, None, Article 18 Filing.
Validation Response eu-3-1 validation-response Marketing Authorisation Application,Variation 1A Filing,Variation 1AIN Filing, Variation 1B Filing, Variation 2 Filing, National Variation Filing, Extension Filing, Repeat Use Procedure, Periodic Safety Update Report, PSUR single assessment procedure, Risk Management Plan Filing, Renewal Filing, Specific Obligation, Related to PAM, Annex II Condition Related to PAM, Additional PV Activity in the RMP Related to PAM, Legally Binding Measure Related to PAM, SDA Submission Related to PAM, Corrective/Preventive Action Related to PAM, Paediatric Submission Related to PAM (Article 45), Paediatric Submission Related to PAM (Article 46), PAES Submission Related to PAM, Recommendation Related to PAM, PASS Protocol Submission (Article 107n), PASS Report Submission (Article 107q), ASMF Filing, Plasma Master File, Article 20 Referral, Article 29(4) Referral, Article 29 Paediatric Referral, Article 30 Referral, Article 31 Referral, Article 35 Referral, Article 5(3) Referral, Article 107i Referral, Article 16c (1c)i Referral, Article 16c(4) Referral, Annual Reassessment Filing, USR Filing, Clinical Data for Publication – Redacted Proposal, Clinical Data for Publication – Final Version, PAED Related to PIP (Article 7, 8, 30), PAED Article 29 Filing, PAED Article 45, PAED Article 46, Article 58 Filing, Notification 61-3 Filing, Transfer MA Filing, Lifting Suspension Filing, Withdrawal Filing, CEP Submission, None, Article 18 Filing.
Response eu-3-1 response Marketing Authorisation Application,Variation 1A Filing,Variation 1AIN Filing, Variation 1B Filing, Variation 2 Filing, National Variation Filing, Extension Filing, Repeat Use Procedure, Periodic Safety Update Report, PSUR single assessment procedure, Risk Management Plan Filing, Renewal Filing, Specific Obligation, Related to PAM, Annex II Condition Related to PAM, Additional PV Activity in the RMP Related to PAM, Legally Binding Measure Related to PAM, SDA Submission Related to PAM, Corrective/Preventive Action Related to PAM, Paediatric Submission Related to PAM (Article 45), Paediatric Submission Related to PAM (Article 46), PAES Submission Related to PAM, Recommendation Related to PAM, PASS Protocol Submission (Article 107n), PASS Report Submission (Article 107q), ASMF Filing, Plasma Master File, Article 20 Referral, Article 29(4) Referral, Article 29 Paediatric Referral, Article 30 Referral, Article 31 Referral, Article 35 Referral, Article 5(3) Referral, Article 107i Referral, Article 16c (1c)i Referral, Article 16c(4) Referral, Annual Reassessment Filing, USR Filing, Clinical Data for Publication - Redacted Proposal, Clinical Data for Publication - Final Version, PAED Related to PIP (Article 7, 8, 30), PAED Article 29 Filing, PAED Article 45, PAED Article 46, Article 58 Filing, Notification 61-3 Filing, Transfer MA Filing, Lifting Suspension Filing, Withdrawal Filing, CEP Submission, None, Article 18 Filing.
Additional Information eu-3-1 additional-info Marketing Authorisation Application,Variation 1A Filing,Variation 1AIN Filing, Variation 1B Filing, Variation 2 Filing, National Variation Filing, Extension Filing, Repeat Use Procedure, Periodic Safety Update Report, PSUR single assessment procedure, Risk Management Plan Filing, Renewal Filing, Specific Obligation, Related to PAM, Annex II Condition Related to PAM, Additional PV Activity in the RMP Related to PAM, Legally Binding Measure Related to PAM, SDA Submission Related to PAM, Corrective/Preventive Action Related to PAM, Paediatric Submission Related to PAM (Article 45), Paediatric Submission Related to PAM (Article 46), PAES Submission Related to PAM, Recommendation Related to PAM, PASS Protocol Submission (Article 107n), PASS Report Submission (Article 107q), ASMF Filing, Plasma Master File, Article 20 Referral, Article 29(4) Referral, Article 29 Paediatric Referral, Article 30 Referral, Article 31 Referral, Article 35 Referral, Article 5(3) Referral, Article 107i Referral, Article 16c (1c)i Referral, Article 16c(4) Referral, Annual Reassessment Filing, USR Filing, Clinical Data for Publication - Redacted Proposal, Clinical Data for Publication - Final Version, PAED Related to PIP (Article 7, 8, 30), PAED Article 29 Filing, PAED Article 45, PAED Article 46, Article 58 Filing, Notification 61-3 Filing, Transfer MA Filing, Lifting Suspension Filing, Withdrawal Filing, CEP Submission, None, Article 18 Filing.
Closing Information eu-3-1 closing Marketing Authorisation Application,Variation 1A Filing,Variation 1AIN Filing, Variation 1B Filing, Variation 2 Filing, National Variation Filing, Extension Filing, Repeat Use Procedure, Periodic Safety Update Report, PSUR single assessment procedure, Risk Management Plan Filing, Renewal Filing, Specific Obligation, Related to PAM, Annex II Condition Related to PAM, Additional PV Activity in the RMP Related to PAM, Legally Binding Measure Related to PAM, SDA Submission Related to PAM, Corrective/Preventive Action Related to PAM, Paediatric Submission Related to PAM (Article 45), Paediatric Submission Related to PAM (Article 46), PAES Submission Related to PAM, Recommendation Related to PAM, PASS Protocol Submission (Article 107n), PASS Report Submission (Article 107q), ASMF Filing, Plasma Master File, Article 20 Referral, Article 29(4) Referral, Article 29 Paediatric Referral, Article 30 Referral, Article 31 Referral, Article 35 Referral, Article 5(3) Referral, Article 107i Referral, Article 16c (1c)i Referral, Article 16c(4) Referral, Annual Reassessment Filing, USR Filing, Clinical Data for Publication - Redacted Proposal, Clinical Data for Publication - Final Version, PAED Related to PIP (Article 7, 8, 30), PAED Article 29 Filing, PAED Article 45, PAED Article 46, Article 58 Filing, Notification 61-3 Filing, Transfer MA Filing, Lifting Suspension Filing, Withdrawal Filing, CEP Submission, None, Article 18 Filing.
Consolidating eu-3-1 consolidating Marketing Authorisation Application,Variation 1A Filing,Variation 1AIN Filing, Variation 1B Filing, Variation 2 Filing, National Variation Filing, Extension Filing, Repeat Use Procedure, Periodic Safety Update Report, PSUR single assessment procedure, Risk Management Plan Filing, Renewal Filing, Specific Obligation, Related to PAM, Annex II Condition Related to PAM, Additional PV Activity in the RMP Related to PAM, Legally Binding Measure Related to PAM, SDA Submission Related to PAM, Corrective/Preventive Action Related to PAM, Paediatric Submission Related to PAM (Article 45), Paediatric Submission Related to PAM (Article 46), PAES Submission Related to PAM, Recommendation Related to PAM, PASS Protocol Submission (Article 107n), PASS Report Submission (Article 107q), ASMF Filing, Plasma Master File, Article 20 Referral, Article 29(4) Referral, Article 29 Paediatric Referral, Article 30 Referral, Article 31 Referral, Article 35 Referral, Article 5(3) Referral, Article 107i Referral, Article 16c (1c)i Referral, Article 16c(4) Referral, Annual Reassessment Filing, USR Filing, Clinical Data for Publication - Redacted Proposal, Clinical Data for Publication - Final Version, PAED Related to PIP (Article 7, 8, 30), PAED Article 29 Filing, PAED Article 45, PAED Article 46, Article 58 Filing, Notification 61-3 Filing, Transfer MA Filing, Lifting Suspension Filing, Withdrawal Filing, CEP Submission, None, Article 18 Filing.
Corrigendum eu-3-1 corrigendum Marketing Authorisation Application,Variation 1A Filing,Variation 1AIN Filing, Variation 1B Filing, Variation 2 Filing, National Variation Filing, Extension Filing, Repeat Use Procedure, Periodic Safety Update Report, PSUR single assessment procedure, Risk Management Plan Filing, Renewal Filing, Specific Obligation, Related to PAM, Annex II Condition Related to PAM, Additional PV Activity in the RMP Related to PAM, Legally Binding Measure Related to PAM, SDA Submission Related to PAM, Corrective/Preventive Action Related to PAM, Paediatric Submission Related to PAM (Article 45), Paediatric Submission Related to PAM (Article 46), PAES Submission Related to PAM, Recommendation Related to PAM, PASS Protocol Submission (Article 107n), PASS Report Submission (Article 107q), ASMF Filing, Plasma Master File, Article 20 Referral, Article 29(4) Referral, Article 29 Paediatric Referral, Article 30 Referral, Article 31 Referral, Article 35 Referral, Article 5(3) Referral, Article 107i Referral, Article 16c (1c)i Referral, Article 16c(4) Referral, Annual Reassessment Filing, USR Filing, Clinical Data for Publication - Redacted Proposal, Clinical Data for Publication - Final Version, PAED Related to PIP (Article 7, 8, 30), PAED Article 29 Filing, PAED Article 45, PAED Article 46, Article 58 Filing, Notification 61-3 Filing, Transfer MA Filing, Lifting Suspension Filing, Withdrawal Filing, CEP Submission, None, Article 18 Filing.
Reformat eu-3-1 reformat Marketing Authorisation Application,Variation 1A Filing,Variation 1AIN Filing, Variation 1B Filing, Variation 2 Filing, National Variation Filing, Extension Filing, Repeat Use Procedure, Periodic Safety Update Report, PSUR single assessment procedure, Risk Management Plan Filing, Renewal Filing, Specific Obligation, Related to PAM, Annex II Condition Related to PAM, Additional PV Activity in the RMP Related to PAM, Legally Binding Measure Related to PAM, SDA Submission Related to PAM, Corrective/Preventive Action Related to PAM, Paediatric Submission Related to PAM (Article 45), Paediatric Submission Related to PAM (Article 46), PAES Submission Related to PAM, Recommendation Related to PAM, PASS Protocol Submission (Article 107n), PASS Report Submission (Article 107q), ASMF Filing, Plasma Master File, Article 20 Referral, Article 29(4) Referral, Article 29 Paediatric Referral, Article 30 Referral, Article 31 Referral, Article 35 Referral, Article 5(3) Referral, Article 107i Referral, Article 16c (1c)i Referral, Article 16c(4) Referral, Annual Reassessment Filing, USR Filing, Clinical Data for Publication - Redacted Proposal, Clinical Data for Publication - Final Version, PAED Related to PIP (Article 7, 8, 30), PAED Article 29 Filing, PAED Article 45, PAED Article 46, Article 58 Filing, Notification 61-3 Filing, Transfer MA Filing, Lifting Suspension Filing, Withdrawal Filing, CEP Submission, None, Article 18 Filing.
Re-examination eu-3-1 re-examination Marketing Authorisation Application,Variation 1A Filing,Variation 1AIN Filing, Variation 1B Filing, Variation 2 Filing, National Variation Filing, Extension Filing, Repeat Use Procedure, Periodic Safety Update Report, PSUR single assessment procedure, Risk Management Plan Filing, Renewal Filing, Specific Obligation, Related to PAM, Annex II Condition Related to PAM, Additional PV Activity in the RMP Related to PAM, Legally Binding Measure Related to PAM, SDA Submission Related to PAM, Corrective/Preventive Action Related to PAM, Paediatric Submission Related to PAM (Article 45), Paediatric Submission Related to PAM (Article 46), PAES Submission Related to PAM, Recommendation Related to PAM, PASS Protocol Submission (Article 107n), PASS Report Submission (Article 107q), ASMF Filing, Plasma Master File, Article 20 Referral, Article 29(4) Referral, Article 29 Paediatric Referral, Article 30 Referral, Article 31 Referral, Article 35 Referral, Article 5(3) Referral, Article 107i Referral, Article 16c (1c)i Referral, Article 16c(4) Referral, Annual Reassessment Filing, USR Filing, Clinical Data for Publication - Redacted Proposal, Clinical Data for Publication - Final Version, PAED Related to PIP (Article 7, 8, 30), PAED Article 29 Filing, PAED Article 45, PAED Article 46, Article 58 Filing, Notification 61-3 Filing, Transfer MA Filing, Lifting Suspension Filing, Withdrawal Filing, CEP Submission, None, Article 18 Filing.

WHO v1.0 Updates

Application Maintenance – Region Values

If the WHO region already exists in the Application Maintenance – Region Values section in Data Administration, it will be updated to have the code value ‘WHO’ in the database. Otherwise, the WHO region will be added with the values:

Region Abbreviation Region Name Active Flag
WHO World Health Organization Active

Application Maintenance - Country Values

The country WHO in the Application Maintenance – Country values in Data Administration, will be changed or added, if absent, with the following values:
Country Code Country Name eCTD Code Region Active Flag
WHO World Health Organization whopqt World Health Organization Active

Application Maintenance - Health Authority Name

Health Authority name for WHO country, in the Application Maintenance – Country values in Data Administration under the Health Authority tab, will be changed or added, if absent, to those listed in the following table:
Country Name Health Authority Name Health Authority Abbreviation Health Authority eCTD Code Health Authority website
World Health Organization World Health Organization WHO whopqt https://extranet.who.int/prequal/

Assembly - Assembly DTD/Schema Type Values

If the 'WHO-1-0' Assembly DTD/Schema type already exists in the Assembly - Assembly DTD/Schema Types section in Data Administration, it will be activated (if inactive) and updated to have the code value 'WHO-1-0'. Otherwise, the 'WHO-1-0' Assembly DTD/Schema will be added.

Application Maintenance - Procedure Type Values

The ‘National’ Procedure Type in the Application Maintenance - Procedure Type values section in Data Administration will be activated (if inactive) and updated to include WHO country, in addition to countries that were already assigned.

Application Maintenance - Application Type Values

The Application Type Values list will be added to the Data Administration > Application Maintenance section if it does not already exist. The list includes the following values:
Application Type Name Display Name Entity XML Type Name Application Category Countries
FPP Finished Pharmaceutical Product Finished Pharmaceutical Product New Drug Application Finished Pharmaceutical Product World Health Organization
FVP Finished Vaccine Product Finished Vaccine Product New Drug Application Finished Vaccine Product World Health Organization
APIPQ Active Pharmaceutical Ingredient Active Pharmaceutical Ingredient New Drug Application Active Pharmaceutical Ingredient World Health Organization
APIMF Active Pharmaceutical Ingredient Master File Active Pharmaceutical Ingredient Master File New Drug Application Active Pharmaceutical Ingredient Master File World Health Organization
The Finished Pharmaceutical Product Application Type gets Default Flag set to Yes upon associating it with WHO country.

Application Maintenance - Application Category Values

Application Category Values will be added to the Application Maintenance – Application Type Values section in Data Administration if they do not already exist. The list of new values can be found in the table below:

Application Category Name Active Flag
Finished Pharmaceutical Product Active
Finished Vaccine Product Active
Active Pharmaceutical Ingredient Active
Active Pharmaceutical Ingredient Master File Active

Application Maintenance - Application Type eCTD Codes

The Application Type eCTD Codes values will be added to the Application Maintenance > Application Type Values list in Data Administration if they do not already exist there. If they exist, the eCTD Code for who-1-0 DTD/Schema will be added to them. The list of new values includes the following:

Application Type (Display Name) Application DTD/Schema eCTD Code Agency Abbreviation Limit to Cross Application Only
Finished Pharmaceutical Product who-1-0 FPP No
Finished Vaccine Product who-1-0 FVP No
Active Pharmaceutical Ingredient who-1-0 APIPQ No
Active Pharmaceutical Ingredient Master File who-1-0 APIMF No

Sequence Maintenance - Filing Type eCTD Codes

The Filing Type eCTD Codes values will be added to the Sequence Maintenance > Filing Type Values list in Data Administration if they do not already exist. If they exist, the eCTD Code for who-1-0 DTD/Schema is added to them. The list of new values includes the following:

Filing Type (Display) Applicable DTD/Schema eCTD Code Available for Application Types
Annual Report (FVP) who-1-0 AR Finished Pharmaceutical Product, Finished Vaccine Product, Active Pharmaceutical Ingredient, Active Pharmaceutical Ingredient Master File
APIMF Procedure who-1-0 APIMF Finished Pharmaceutical Product, Finished Vaccine Product, Active Pharmaceutical Ingredient, Active Pharmaceutical Ingredient Master File
New Emergency Use Listing (EUL) Application (FPP, FVP) who-1-0 EUL Finished Pharmaceutical Product, Finished Vaccine Product, Active Pharmaceutical Ingredient, Active Pharmaceutical Ingredient Master File
Post-PQ Change (API, FFP, FVP) who-1-0 PPQC Finished Pharmaceutical Product, Finished Vaccine Product, Active Pharmaceutical Ingredient, Active Pharmaceutical Ingredient Master File
New Prequalification Application (API, FFP, FVP) who-1-0 PQP Finished Pharmaceutical Product, Finished Vaccine Product, Active Pharmaceutical Ingredient, Active Pharmaceutical Ingredient Master File
Reassessment (FVP) who-1-0 REAS Finished Pharmaceutical Product, Finished Vaccine Product, Active Pharmaceutical Ingredient, Active Pharmaceutical Ingredient Master File
Requalification Application (FPP) who-1-0 RQAP Finished Pharmaceutical Product, Finished Vaccine Product, Active Pharmaceutical Ingredient, Active Pharmaceutical Ingredient Master File

Submission Maintenance - Sub Filing Type eCTD Codes

The Sub Filing Type eCTD Codes values will be added to the Submission Maintenance > Sub Filling Type Values section in Data Administration if they do not already exist. If they exist, the eCTD Code for who-1-0 DTD/Schema is added to them. The list of new values includes the following:

Sub Filing Type (Display Name) Applicable DTD/Schema eCTD Code Available for Filing Type
Annual Notification (FPP) WHO-1-0 AN Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
Abridged WHO-1-0 PQA Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
Immediate Notification (API) WHO-1-0 AIN Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
Annual Notification (API) WHO-1-0 AAN Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
Conversion WHO-1-0 CONV Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
eCTD Baseline WHO-1-0 eCTDB Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
EUL-Full (Emergency Use Listing) WHO-1-0 EULF Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
Full WHO-1-0 Full Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
Immediate Notification (FPP) WHO-1-0 IN Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
Major WHO-1-0 Major Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
Minor WHO-1-0 Minor Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
Parallel WHO-1-0 Parallel Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
Product Extension WHO-1-0 PEX Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
Standard WHO-1-0 STD Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
Type A (Approval Before Implementation)(Major)(FVP) WHO-1-0 AMAJ Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
Type N (Immediate Notification)(Minor) (FVP) WHO-1-0 NMI Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
Update WHO-1-0 UPD Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
no Application Sub Type WHO-1-0 none Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)
EUL-Abridged (Emergency Use Listing) WHO-1-0 EULA Annual Report (FVP), APIMF Procedure, New Emergency Use Listing (EUL) Application (FPP,FVP), Post-PQ Change (API, FFP, FVP), New Prequalification Application (API, FFP, FVP), Reassessment (FVP),Requalification Application (FPP)

Submission Maintenance - Regulatory Activity Lead Values

The Regulatory Activity Lead Values will be added to the Submission Maintenance > Regulatory Activity Lead Values list in Data Administration if they do not already exist. The list of new values includes the following:
Region Applicable DTD/Schema eCTD Code Regulatory Activity Lead
WHO who-1-0 initial Initial
WHO who-1-0 validation-response Validation Response
WHO who-1-0 response Response
WHO who-1-0 additional-info Additional Info
WHO who-1-0 reformat Reformat

Submission Maintenance Submission Product Type Values

Submission Product Type values will be added to the Submission Maintenance > Submission Product Type Values section in Data Administration if they do not already exist. The list of new values can be found in the table below:

Region eCTD Code Product Type Applicable DTD/Schema
WHO BTP Biotherapeutic Product WHO-1-0
WHO FPP Finished Pharmaceutical Product WHO-1-0