FDA documents

 
Containers:
Box 19 (MS 8696)
Component identifier:
File 1
Content Summary:
[Reports, Patient consent forms, Correspondence. Reports include: `Clinical trial protocol for patients receiving a multiple-channnel cochlear implant', `Device exemption to the Food and Drug Administration for a significant risk device', `FDA guidelines on preparing reports'; Patient consent forms: `Informed patient consent regarding a clinical investigation study of implantable hearing prosthesis required by USA Food and Drug Administration'; Inwards and outwards correspondence with: P.K. Wood (University of Melbourne), C. Bunn, R.K. Shepherd (UNDOL)] 1982

Access and use

Location of this collection:
Parkes Place
Canberra ACT 2600, Australia
Contact: