Carta de autorización (LoA) — Encuentre soporte para hacer carta de autorización

Para un proceso de solicitud de medicamentos eficiente, solicite su LOA ahora

Modelo de carta de autorización

La carta de autorización farmacéutica otorga permiso a la agencia gubernamental para consultar los Drug Master Files (DMF). Es una declaración escrita realizada por un representante en soporte de la presentación de otra entidad. SCHOTT Pharma puede darle soporte para hacer carta de autorización y garantizar que su proceso de solicitud de medicamentos se complete sin problemas. Para enviar una solicitud, utilice el formulario de carta de autorización:

Formulario de carta de autorización

Submit LOA-Request

Submission Details

Country Of Submission *

Full company name incl. legal entity. Otherwise your LOA might be rejected by the authorities.

Company Name *

Company Name China (In China, only relevant to China submission. If there is no corresponding Chinese translation of your Company Name or there is no Company Name in Chinese, please use your English Company Name) *

Address 1 (Please provide Postal address in English) * Address 2 City * State/Province * Zip/Postal Code * Country * First Name * Last Name * Title Phone Country Code * Phone Area Code * Phone *

E-mail *

Is the company for whom the LOA is being issued the same as the requesting company? If not, please add additional company by clicking checkbox.

Issue LOA for the following company:

Company Name *

Company Name (in Chinese, only relevant for China Submission)

Address 1 * Address 2 City * State/Province * Zip/Postal Code * Country * First Name * Last Name * Title Phone Country Code * Phone Area Code * Phone * E-mail *

Your Drug Product Name

Drug Product Name/Active Ingredient *

SCHOTT Product Details

SCHOTT Product Manufacturing Facility *

SCHOTT Product Group *

SCHOTT Product Description (e.g. pen cartridge 20ml) * SCHOTT Article No. (7-digit starting with 1... )

Specification/model* (Please kindly enter the format or size of the container(s) used, e.g. 2 mL) *

Information of Drug to be applied at the NMPA in China (China Submission), (Should be identical to the name given in the submission dossier to NMPA)

Name of the drug (in English) * Name of the drug (in Chinese)* (If there is no corresponding Chinese translation or Chinese Name of the Drug, please enter Name of the Drug in English into this field) * Route of administration (in English) * Route of administration (in Chinese) *

Comments

Comments Please enter the numer of originals of the requested China LoA

Comments

Please enter the number of originals of the requested China LoA; if no hard copy is needed, please enter ’No original/hard copy is required’ in this field.*

First Name Last Name E-mail Phone Number