How to register APIs in Brazil - Online Training Recording

Costs

*ECA-Member:**	EUR 590,--
*Regular Fee:**	EUR 690,--
*EU/GMP Inspectorates:**	EUR 590,--
*APIC Member Discount:**	EUR 640,--

(All prices excl. VAT). Important notes on sales tax.

Registration

* also payable by credit card

If you have any questions, please contact us:
Tel.: +49 (0)6221 / 84 44 0 E-Mail: info@concept-heidelberg.de

Speakers

Marieke van Dalen, Global Regulatory Specialist
Susan Swiggers, Aspen Oss, Customer & Regulatory Support Officer

Background

Since August 2020, the “CADIFA Manual of Administrative Procedures” of the Brazilian Health Regulatory Agency (Anvisa) is valid and needs to be followed for API dossiers. Now, the new version of the “CADIFA Manual” is published and available in Portuguese and in English language.¹

According to the agency, the DIFA (Active Pharmaceutical Ingredient dossier) must be submitted to Anvisa by the DIFA holder to receive a CADIFA (letter of suitability of the active pharmaceutical ingredient). It shows the compliance of a DIFA with the regulatory requirements. A valid CADIFA and GMP certificate are necessary for the approval of an associated marketing authorization or post-approval change application.¹

The understanding of Brazilian Registration Procedures for APIs is thus important to know. This Live Online Training provides an overview of the regulatory and GMP requirements for registering APIs in Brazil and obtaining the Brazilian GMP certificate.

¹ Source: CADIFA Manual for Administrative Procedures, CADIFA Manual nº 01, 2nd Version

Target Group

This Live Online Training has been developed for all who are dealing with API Sourcing, Manufacturing, Quality Assurance and Regulatory Affairs.

Technical Details:

To participate in an on demand training course or webinar, you do not need any software. The recordings are made available via a streaming server. In general, the recording is provided in MP4 format, which any PC (Microsoft Windows, Apple IOS) or tablet can easily display.

Timing and Duration:
When you register for the on demand Training course or webinar you can decide at what date you want to follow the training course online. For a 1-day training course you will have 2 days in which the stream is available (for 2-day training course 3 days and for a 3-day training course 4 days). Within in this timeframe you can start & stop the stream according to your needs.

In time before the scheduled date (your desired date) you will receive an e-mail from us with a link for direct participation as well as your log-in data.

Please be aware: The recording does not include the Q & A sessions.

Training Course Documentation and Certificate:
The presentations will be made available as PDF files via download shortly before the online training course. After the event, you will automatically receive your certificate of participation.

Programme

How to Handle Brazilian Registrations

Different ways of submitting API Information
Procedural aspects
Guidelines

Content of the Registration File

The CADIFA System
The DIFA (API dossier)
What is different from other regions?

Handling Changes in Brazil

Relevant guidelines
How does it work in practice

Obtaining the Brazilian GMP Certificate

Starting the GMP certificate procedure
Different sites & different classes of products

Recording from 28 February 2023

Duration of Recording 2 h 10 min

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