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CERTIFICATION OF CHIEF EXECUTIVE OFFICER OR EQUIVALENT PURSUANT TO SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002 SUBSECTIONS a ; AND b ; OF SECTION 1350, CHAPTER 63 OF TITLE 18 UNITED STATES CODE ; Pursuant to section 906 of the Sarbanes-Oxley Act of 2002 subsections a ; and b ; of section 1350, chapter 63 of title 18, United States Code ; , the undersigned officer of DRAXIS Health Inc., a corporation incorporated under the laws of Canada the "Company" ; , hereby certifies, to such officer's knowledge, that: The Annual Report of Form 20-F for the year ended December 31, 2006 the "Report" ; of the Company fully complies with the requirements of section 13 a ; or the Securities Exchange Act of 1934 and information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.

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Synopsis This story from BMJ news focuses on a report on the former MCA by the House of Commons Committee of Public Accounts. In the report, entitled "Safety, Quality, Efficacy: Regulating Medicines in the UK", the MCA is criticised for it's "lack of dynamism" in improving public health and for its "non-existent" public profile, which made it hard for it to function as a source of safety information. In April 2003, the MCA merged with the Medical Devices Agency MDA ; to form the Medicines and Healthcare Products Regulatory Agency MHRA ; , which now has taken on the responsibilities of the MCA. The committee looked at the MCA's performance against its key objectives of promoting and safeguarding public health through the regulation and provision of information on medicines, and its service to stakeholders. The report was critical of the poor quality of information leaflets and labels, designed to alert patients and doctors to potential risks of medication, and the low level of reporting of adverse reactions to medicines by doctors. These were quoted as evidence of the lack of dynamism to push further improvements in the protection of public health. Additionally, the report mentions that the widespread but unmonitored practice of prescribing drugs to children that, although licensed, were not specifically approved for paediatric use was also cause for concern. The committee also highlighted the irony that an agency whose aim was to relay safety messages to the public had a non-existent public profile. Doctors were even found to have only little knowledge of its role. The report adds that in contrast to the American FDA, the MCA did not support advertising and awareness campaigns required for developing a relationship with the public. The committee hopes that the creation of the Medicines and Healthcare Products Regulatory Agency will be a good opportunity to correct some of the failings of its predecessor. It wants to see the new body develop training for doctors on monitoring the safety of medicines, as well as establishing an effective communications and awareness strategy for conveying safety messages both to the public and to health practitioners. Safety, Quality, Efficacy: Regulating Medicines in the UK 26th sixth report of session 2002-3 ; is available at parliament and glimepiride and sumycin, because drug information.

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