Life Sciences Insights

22 November 2004

Welcome to the November edition of Clayton Utz Life Sciences Insights. In this edition we look at the proposal to require manufacturers' details on medicines, and what's next in labeling regulation.

We'll also find out the latest in the development of a national regulatory framework for human cell and tissue therapies, and the regulatory problems surrounding gene patenting.

Finally, we'll look at the draft Code which helps listed biotech companies make disclosures as required by the ASX.

Future regulation of cell and tissue therapies

By Robyn Baker and Janine Jansen.

A new regulatory framework for human cell, tissues and cellular and tissue-based products is being developed. Robyn Baker and Janine Jansen see where the process is at.

Proposed changes to medicine labelling requirements following the Pan recall

By Robyn Baker and Mia Livingstone .

The Pan recall revealed some of the problems with our current labelling system. The work done by the Therapeutic Goods Committee on the possible mandatory inclusion of manufacturers' names on medicines will play a part in the review of these issues presently being conducted by an expert Committee on Medicine Labelling, say Robyn Baker and Mia Livingstone.

ASX paves the way for self-regulation of the biotech industry

By Anna Sharpe and Georgina Johnson.

When, how, and how much should listed biotech companies make disclosures as required by the ASX? Anna Sharpe and Georgina Johnson look at a new draft Code which is intended to provide guidance.

International recognition for our Life Sciences team

Global Counsel has ranked our Life Sciences 11th globally.

To view claytonutz.com correctly, you should upgrade your browser