VM3: Navigating the regulatory landscape of veterinary product information

By Catarina Ferreira2024-11-08T06:57:00

Key points:

The session highlighted the complexity of implementing changes in product information (PI) required by Regulation (EU) 2019/6, QRD template v9.0, and related new legal acts
Both regulators and the industry expressed concerns about meeting the 2027 deadline, emphasising the need for careful planning and harmonisation of assessment processes to ensure timely completion

To read more key points and the session summary, log in as a member or register for free using the links below.

How to read this journal article

Thank you for visiting Regulatory Rapporteur. Journal articles are restricted to TOPRA members and registered users.

If you are a TOPRA member, or have already registered for limited free access, log in now (Option 1 below).

Not yet a member? You can either join TOPRA (Option 2 below) or register to view limited content for free (Option 3 below).

1. LOGIN

Already a TOPRA member?

Log in now using your MyTOPRA credentials, for unlimited access to all Regulatory Rapporteur journal articles, the online archive and latest industry news and podcasts.

Renew your TOPRA membership for 2026 here.

Already registered for free content?

If you are not a TOPRA member but have already created an account to access limited free content, log in here using your registered user email and password.

2. JOIN TOPRA

TOPRA membership

Become a TOPRA member and join our global regulatory affairs community.

Great savings on our events and training.
Be part of our dynamic international community.
Contribute to the profession.
Grow your skills and knowledge.
Take your career to the next level.

Become a member

3. REGISTER FOR FREE

Want free access to selected content?

Register now to continue to access industry news, editorials and podcasts plus one member-only journal article each month.

Create your own library to save your favourite content.

Create a free account