date:Nov 07, 2012
uld not be necessary if it contained ingredients previously used and additives that were permitted.
The next speaker was Dr Gert Krabichler, head, global regulatory affairs, global RD / department, Merck Consumer Healthcare Holding GmbH. He spoke about the EU regulations regarding product approval. He informed about health claims and explained the regulation process as far as EU was concerned.
Continuing on same grounds, next speaker Prabodh Halde, head, technical regulatory Affairs, Marico,