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

Event Details

Time: December 5, 2018 at 10am to December 12, 2018 at 11am
Location: Online
Street: 161 Mission Falls Lane, Suite 216,
City/Town: https://www.compliance4all.com/control/w_product/~product_id=502215LIVE?channel=medtechiq_Dec_2018_SEO
Website or Map: https://www.compliance4all.co…
Phone: Event Manager
Event Type: webinar
Organized By: Adam Fleming
Latest Activity: Oct 10, 2018

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Event 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: support@compliance4All.com