Quality Counts in Healthcare Products
Recently at an pharmaceutial industry based conference, I was reminded of the upcoming regulation changes being considered in the draft GMPs ( Good Manufacturing Practices) Guidelines for 2007. For those in the pharmaceutical (drug), radiopharmaceutical, biological, and veterinary drugs industy, the GMPs are the governing requirements for maintaining an Establishment Licence in Canada and a well known if not always well understood, monitored (via regulatory audits) "guidance" for this industy. For those not in the industry, consider yourselves fortunate that you are not subjected to regularly scheduled scrutiny of your business operation and quality governing principles and practices. A regulatory audit and review of compliance to the guidelines can be a frequent occurance depending on the changes going on in your organization. Yes, compliance to a ''guideline" .....though there is no option! So what can we expect to see under scrutiny for the 2007 GMP changes?
Continue reading "Quality Counts in Healthcare Products" »
Social Bookmarking:
Digg,
delicious,
reddit,
NewsVine,
Furl,
Fark,
Google,
Spurl,
BlinkList,
Simpy,
StumbleUpon,
BlogMarks,
Facebook