Vendor-CRO-CMO Oversight in the (Biopharma) and Device Industry
Added by Compliance4all on 2018-10-08
Conference Dates:
Start Date: 2018-12-05Conference Contact Info:
Contact Person: Event ManagerEmail: [email protected]
Address: 161 Mission Falls Lane, Suite 216,, Fremont, California, 94539, United States
Tel: 18004479407
Fax: 302-288-6884
Conference Description:
Overview:This webinar is specifically designed for sponsoring biopharma and device
companies who are outsourcing.It will help you get to grips with effective
Vendors (including CRO,CMO, and other vendors) management used in
the biopharma and device industries and your responsibilities as the
sponsor.
Areas Covered in the Session:
Setting up vendor oversight
Inspector expectations
Selection of CROs to meet oversight requirements
Ensuring clarity of roles and responsibilities
RFI and RFP
Contractual consideration for oversight
The oversight/quality plan
Who Will Benefit:
Regulatory
Manufacturing
Pharmacovigilance
Compliance
Audit
Quality
Speaker Profile:
Dr. Laura Brown , PhD, MBA, Diploma Clinical Sciences, is an independent
QA and training consultant in the pharmaceutical industry. She is a
managing director with LB Training and Development Ltd., course director
for the M.Sc. in Clinical Research, School of Pharmacy at the University of
Cardiff, and course director for M.Sc. Regulatory Affairs, TOPRA.
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]