Endodontic sterilisers to be regulated as Class III devices
This article was originally published in Clinica
PMAs or a notice of completion of a product development protocol will be required for endodontic dry heat sterilisers under a proposed classification change by the US FDA. The agency is inviting comments by September 5th, 1995, on the proposed rule published in the Federal Register on June 7th.
You may also be interested in...
Becton Dickinson will spend $1.2bn over the next four years to improve its drug-delivery device manufacturing capabilities. See what Eric Borin, president of BD, said about it here.
Pfizer is producing vaccine doses at scale now that it has buttoned down the manufacturing process.
In second letter this year targeting email communications, OPDP says that putting the methotrexate oral solution’s risk information below the signature block does not offer ‘prominence and readability’ comparable to the information on the drug’s effectiveness for the treatment of acute lymphoblastic leukemia that was in the body of the email.