Release 4.66.0 MDLP February 1, 2025

Information about the content of the release in Russian can be found at this link

Installed on the Sandbox test environment: 29.01.2025

Installed on the production environment: 01.02.2025

XSD-schemes version: 1.38

Modifications

Added the “Export type” parameter into the general report on disposal

The “Export type” parameter was added into the “General report on disposal” report in a medicine circulation participant’s user account. The parameter can take one of the following values:

• “—” (no value);

• “Export to Uzbekistan”;

• “Export to third countries”;

• “Shipment of medicines in EAEU”.

Added the “Manufacturer indicated on the packaging of the medicine” parameter into a registry and card of the medicine

The “Manufacturer indicated on the packaging of the medicine” parameter (the column is hidden by default) was added into the “Medicines” → “Registry of medicines” in a medicine circulation participant’s user account. The new parameter was also added into a card of the medicine and is available in case of export of the registry.

To fill in or edit this field, go to the section “Medicines” → “Registry of medicines” → “Adjust”, then you will see a modal window — “Create request for medicine data correction”. The new parameter was added as well into the registry of requests for medicine data correction: “Medicines” → “Registry of requests for medicine data correction”.

Now the new field is optional. If you modify this field, it is necessary to attach a photo of the secondary package of the medicine for subsequent changes approval. Information about a manufacturer from this field will be displayed in a medicine card in Chestny ZNAK app.

New status transitions for schemes 552/23 and 391/1/16

The following status transitions were added for scheme 552 (“Registration in MDLP IS of information about medicinal drugs withdrawal from circulation for various reasons”) with a type of withdrawal from circulation 23 (“withdrawn from circulation in view of the write-off when there is no information according to BP”):

• in_realization (“Shipped”) → out_of_circulation (“Withdrawn from circulation”);

• transferred_to_agent (“Shipped under agent contract”) → out_of_circulation (“Withdrawn from circulation”);

• change_owner_state_gov (“Awaiting confirmation of receipt by new owner”) → out_of_circulation (“Withdrawn from circulation”).

A possibility to write off expired SGTINs was added for all status transitions for 552/23.

The following status transitions were added for scheme 391 (“Registration in MDLP IS of information on re-introduction of medicine into circulation”) for medicines of good quality and with a reason of withdrawal from circulation 16 (“withdrawn from circulation in view of the write-off when there is no information according to BP”):

• out_of_circulation (“Withdrawn from circulation”) → in_realization (“Shipped”);

• out_of_circulation (“Withdrawn from circulation”) → transferred_to_agent (“Shipped under agent contract”);

• out_of_circulation (“Withdrawn from circulation”) → change_owner_state_gov (“Awaiting confirmation of receipt by new owner”).

Expiration date checks were added for all status transitions for 391/1/16 after 552/23. Only unexpired medicines of good quality can be returned into circulation. Return of substandard medicines by using scheme 391 after scheme 552 is prohibited.

Updated list of the essential software needed for using a user account

Support of the deprecated browsers and operating systems has been discontinued. The following software requirements are established:

• operating system:

• Windows 10 or higher;

• macOS 10 or higher.

• browser:

• “Safari” 14 or higher;

• “Google Chrome” 90 or higher;

• “Yandex Browser” 24 or higher.

Added “Controlled substances attribute” parameter into the registry of medicines and general registry of registered medicines

The “Controlled substances attribute” parameter was added in a medicine circulation participant’s user account into the following sections:

• “Medicines” → “Registry of medicines”;

• “Medicines” → “General registry of registered medicines”.

An attribute of controlled substances is available in case of export of the registry.

API modifications

Added the new field — “Export type” into the “General report on disposal” export

A new field — “Export type” was added into the “General report on disposal” analytical export (GENERAL_REPORT_ON_DISPOSAL). This field can take the following values:

•  “—” (no value);

• “Export to Uzbekistan”;

• “Export to third countries”;

• “Shipment of medicines in EAEU”.

We remind you that you can obtain analytical exports by using the following API methods:

• “Method of creation of new export task”;

• “Method for obtaining a status of export task”;

• “Method for getting the statuses of tasks for export”;

• “Method for getting final data export identifiers”;

• “Method of export obtainment”.

New output parameter — “Manufacturer indicated on the packaging of the medicine”

The “manufacturer” output parameter (“Manufacturer indicated on the packaging of the medicine”) was added into the following methods:

• “Method for obtaining detailed information about a medicine manufactured by the company”;

• “Method for obtaining public information about the manufactured medicine”;

• “Method for obtaining information from the registry of medicines manufactured by the company”.

Filtering by an attribute of controlled substances is available

The “is_pku” (“Controlled substances” attribute) attribute contains a correct value and can be used for filtering in the following methods:

• “Method for obtaining information from the registry of medicines manufactured by the company”;

• “Method for obtaining detailed information about a medicine manufactured by the company”;

• “Method for searching public information in the registry of the manufactured medicines”;

• “Method for obtaining public information about the manufactured medicine”.