European Medicines Agency (EMA) just admitted today (8 Jan 2025) in a "concept" paper in a "Problem Statement", that ;;;;;;;;;;

- Development/manufacturing of mRNA vaccines for veterinary have "no guideline which reflects quality requirements for regulators and industry on mRNA containing vaccines"

Worse, 4 years after authorizing mRNA vaccines &;;;;;;;;;; promoting these vaccines to millions of Europeans they state:

- "mRNA vaccines and their manufacturing process are a novel technology, and the resulting products differ from other types of vaccines"

You've read that right, they just admitted that these mRNA interventions are...novel, in other words: experimental!

Then provides key factors that need regulation/control in the manufacturing of mRNA vaccines for vet use, including:

"Purity control strategy: process-related and product-related impurities as well as other potential contaminants and methods to control them"