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Updates to the Single Window IID ECCRD, Version 4.0

The purpose of this notice is to advise Trade Chain Partners (TCPs) of changes to the IID. On April 13, 2021, the following changes will be made in the production environment:

  1. Fisheries and Oceans Canada – Country of Source data requirements:

It has been brought to the Canada Border Services Agency’s (CBSA’s) attention that the Canadian Food Inspection Agency (CFIA) and the Department of Fisheries and Oceans (DFO) are both utilizing SG118 to capture country of source data on Single Window (SW) IID entries. CFIA has very specific policy surrounding what constitutes the “country of origin” and “country of source”. When the DFO on-boarded to SW, SG118 was included in their data map to capture the “country of origin” and the “country of source” as it relates to their regulations. However, the usage of the country of source data element does not always align with CFIA’s regulations. This has resulted in CFIA issuing rejects when an IID is co-regulated between CFIA and DFO.

Upon review of DFO's data requirements, it was determined that each SW DFO program is already collecting the country in which the goods have been grown, harvested, manufactured, processed, produced and/or slaughtered in the various parties collected in SG119.NAD or SG143.NAD. As a result, the country of source data requirements will be removed from each of the following DFO Appendices:

a) B4.1 Aquatic Biotechnology Program

IID Segment & Tags

Data Element Name

PGA Element Name

Data Element Status

Data Element Rules and Conditions

Qualifier

Codes

SG118
LOC
(Q) 3227
(E) 3225

Country of Source

Country of Source

C

The country in which the goods have been grown, harvested, manufactured, processed, produced or slaughtered must be provided, if different than the Country of Origin and/or Country of Source provided in SG104.

30

 

b) B4.2 Aquatic Invasive Species Program

IID Segment & Tags

Data Element Name

PGA Element Name

Data Element Status

Data Element Rules and Conditions

Qualifier

Codes

SG118
LOC
(Q) 3227
(E) 3225

Country of Source

Country of Source

C

The country in which the goods have been grown, harvested, manufactured, processed, produced or slaughtered must be provided, if different than the Country of Origin and/or Country of Source provided in SG104.

30

 

SG118
LOC
(E) 3223

State of Source

DFO
State of Source

C

The state in which the goods on this commodity line have been grown, harvested, manufactured, processed, produced or slaughtered.
This must be provided if the Country of Source qualifier is used on this commodity line and the country of source is the United States.

   

c) B4.3 Trade Tracking Program (Fisheries Resource Management)

IID Segment & Tags

Data Element Name

PGA Element Name

Data Element Status

Data Element Rules and Conditions

Qualifier

Codes

SG118
LOC
(Q) 3227
(E) 3225

Country of Source

Country of Source

C

The country in which the goods have been grown, harvested, manufactured, processed, produced or slaughtered must be provided, if different than the Country of Origin and/or Country of Source provided in SG104.

30

 

SG118
LOC
(E) 3223

State of Source

US

State of Source

C

The state in which the goods for this commodity have been grown, harvested, manufactured, processed, produced or slaughtered.
This must be provided if the Country of Source qualifier is used on this commodity line and the country of source is the United States.

   
  1. Global Affairs Canada – Shipment Specific and GIP LPCO exemptions:

There are some commodities that are regulated by Global Affairs Canada that are exempt from having to obtain/submit a shipment specific or General Import Permit (GIP). This exemption is dependent on the country of origin and relates to negotiated Free Trade Agreements and applies to certain HS codes that are regulated under GAC’s Beef and Veal and Agriculture Products programs. As a result, system changes have been made to SW validation rules to accommodate these exemptions.

For more information, refer to GAC’s Handbook of Export and Import Commodity Codes.

  1. Health Canada Donor Semen and OVA Program

The CBSA has been advised by Health Canada (HC) that amendments were made to their Safety of Sperm and Ova Regulations earlier in 2020. Currently, the Donor Semen Program in SW does not include any requirements for the importation of ova. As a result, the following changes have been made to appendix B6.5 of the SWI ECCRD:

a) Amend the title of appendix B6.5 to: Donor Semen and Ova Program
b) Amend the introductory paragraph for the program (section B6.5.1), last sentence to: These activities apply to all drugs and devices as defined by the Food and Drugs Act, including donor semen and ova for assisted conception.
c) Add Safety of Sperm and Ova Regulations and Assisted Human Reproduction Act to list of legislative references (section B6.5.1).
d) LPCO document type 5009 (formerly Semen Processor Declaration) will be renamed: Semen or Ova Establishment Attestation
e) New LPCO document type 5048 will be created for Establishment Notification Form (FRM-0446)
f) New LPCO document type 5049 will be created for Establishment Registration Number
g) LPCO document type 5008 (formerly Donor Semen Letter of Authorization (LOA)) will be renamed: Donor Semen or Ova Letter of Authorization (LOA)
h) Canadian Product Category code HC04 will be renamed: Donor Semen or Ova

The following changes have been applied to section B6.5.2:

IID Segment & Tags

Data Element Name

PGA Element Name

Data Element Status

Data Element Rules and Conditions

Qualifier

Codes

SG9
DOC
1131

Canadian Document Type (Licence, Permit, Certificate, Other)

LCPO Type / Authorization Type

C

The coded identifier of applicable document types being provided at the declaration level must be provided in this field. Document types provide here must be applicable to all commodities on this declaration. If not applicable to all commodities, please provide the document types at the commodity line level (SG121). Acceptable document types depend on the intended use. Use (SG117 APP) and Canadian Product Category (SG117 PG) provided:

Intended Use

Canadian Product
Category (SG117 PGI)

Document Type(s)
(SG9 or SG121)

Human Therapeutic Use

Donor Semen or Ova

Semen or Ova Establishment Attestation or

 

Establishment Notification Form (FRM-0446) or

 

Establishment Registration Number

Special Access

Donor Semen or Ova

Donor Semen or Ova Letter of Authorization (LOA)

 

5009

5048

5049

5008

SG9
DOC
1004

LPCO Reference Number

LPCO Number

C

For each document provided at the declaration level, the associated reference number related to that document must be provided.

Document Type(s)

Reference Number

Semen or Ova Establishment attestation

Provide generic LPCO
Number ‘XXX

Establishment Notification Form (FRM-0446)

Provide generic LPCO
Number ‘XXX

Establishment Registration Certificate Number

Provide Registration Certificate Number (######)

Donor Semen or Ova Letter of Authorization (LOA)

Provide generic LPCO
Number ‘XXX’

   

SG9
DOC
1336

Image URN

File

C

If provided at the declaration level, the unique identifier of a related image for the following documents must be provided:

 

  • HC – Semen or Ova Establishment attestation
  • Establishment Notification Form (FRM-0446)
  • Establishment Registration Number
  • HC - Donor Semen or Ova Letter of Authorization (LOA)
 

(URN)

SG117
PGI
Q) 5389
(E) 5388

Canadian

Product Category

Commodity

Type

M

Canadian Product Category must be provided depending on the Intended

End-Use Code entered in SG117 APP as follows:

Intended Use
(SG117 APP)

Canadian Product Category

Human Therapeutic Use

Donor Semen or Ova

Special Access

The qualifier for field 5389 should be the code for HC – Donor Semen or Ova

HC04

HC04

SG117
APP
(Q) 9049
(E) 1131

Intended End-Use

Intended Use

M

The intended end-use of the commodity must be provided. Depending on the intended end-use code, additional details are required as follows:

Intended Use

Canadian Product Category (SG117 PGI)

Document Type(s)
(SG9 or SG121)

Human Therapeutic Use

Donor Semen or Ova

Semen or Ova Establishment Attestation or

 

Establishment Notification Form (FRM-0446) or

 

Establishment Registration Number

Special Access

Donor Semen or Ova

Donor Semen or Ova Letter of Authorization (LOA)

ZZZ

HC01

HC02

SG121
DOC
1131

Canadian Document Type (Licence, Permit, Certificate, Other)

LPCO Type/ Authorization Type

C

The coded identifier of any applicable document must be provided in this field if applicable to a specific commodity line entry. If applicable to all commodities, please provide the documents at the declaration level (SG9). Acceptable documents types depend on the Intended Use (SG117 APP) and Canadian Product Category (SG117 PGI) provided:

Intended Use

Canadian Product Category (SG117 PGI)

Document Type(s)
(SG9 or SG121)

Human Therapeutic Use

Donor Semen or Ova

Semen or Ova Establishment Attestation or

 

Establishment Notification Form
(FRM-0446) or

 

Establishment Registration Number

Special Access

Donor Semen or Ova

Donor Semen or Ova Letter of Authorization (LOA)

 

5009

5048

5049

5008

SG121
DOC
1004

LPCO Reference Number

LPCO Number

C

For each document provided at the declaration level, the associated reference number related to that document must be provided.

Document Type(s)

Reference Number

Semen or Ova Processor Establishment attestation

Provide generic LPCO
Number ‘XXX

Establishment Notification Form (FRM-0446)

Provide generic LPCO
Number ‘XXX

Establishment Registration Certificate Number

Provide Registration Certificate Number (######)

Donor Semen or Ova Letter of Authorization (LOA)

Provide generic LPCO
Number ‘XXX’

 

   

SG121
DOC
1336

Image URN

File

C

If provided at the commodity level, the unique identifier of a related image for the following documents must be provided:

 

  • HC – Semen or Ova Establishment attestation
  • Establishment Notification Form (FRM-0446)
  • Establishment Registration Number
  • HC - Donor Semen or Ova Letter of Authorization (LOA)
 

(URN)

SG125
RCS
(Q) 3055
(E) 7295

PGA Compliance Statement Code

Processor Declaration

C

For importations intended for human therapeutic use (SG117 APP), the code indicating the semen or Ova notification of the product (as indicated below) as per s.4 and s.18 of the Safety of Sperm and Ova Regulations must be provided.

"The shipping container in which the semen or Ova is transported should be accompanied with an Establishment attestation , signed by the establishment senior executive officer, certifying that: the Establishment proposes to import or distribute sperm or ova and the projected start date, the Establishment meets the requirements of the Safety of Sperm and Ova regulations, that all information needed is complete and the Senior Executive officer has the authority to bind the Establishment.

12

HC01

Please note, while system changes have been made to accommodate the new ova regulations, the renaming of LPCO document types 5008/5009 and renaming of product category code HC04 will allow IID clients to continue processing Donor Semen regulated IIDs as they do today.

  1. Transport Canada – Vehicle Classification Code ‘TC1512’

Transport Canada (TC) advised CBSA that they require an edit to the name of vehicle classification code TC1512. “Restricted Use Motorcycle” has been changed to “Restricted Use Vehicle,” across all TC vehicle programs.

If there are any questions related to these changes, clients should contact the OGD Programs Unit: [email protected]

Topic(s)

Other Government Departments (OGDs) Requirements
Release

Information source

Canada Border Services Agency (CBSA)
Disclaimer

The foregoing information is provided for informational purposes only and is not intended as, nor should it be considered, professional advice or a substitute for conducting your own thorough research and review. Before making any decisions or taking any action based on the information provided, you should conduct your own independent investigation and/or seek professional advice from a qualified expert in the relevant field. The CSCB disclaims all liability for actions taken or not taken based on the information provided.