Vendor-CRO-CMO Oversight in the (Biopharma) and Device Industry

Added by Compliance4all on 2018-10-08

Conference Dates:

Start Date Start Date: 2018-12-05

Conference Contact Info:

Contact Person Contact Person: Event Manager
Email Email: [email protected]
Address Address: 161 Mission Falls Lane, Suite 216,, Fremont, California, 94539, United States
Phone Tel: 18004479407
Phone 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]
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