What Sponsors Expect and How to Meet their Expectations

6 years ago Posted By : User Ref No: WURUR19932 0
  • Image
  • TypeWebinar
  • Image
  • Location Fremont, California, United States
  • Price
  • Date 08-06-2018
Webinar Title
What Sponsors Expect and How to Meet their Expectations
Event Type
Webinar
Webinar Date
08-06-2018
Last Date for Applying
05-06-2018
Location
Fremont, California, United States
Organization Name / Organize By
Netzealous LLC DBA - Compliance4All
Organizing/Related Departments
Compliance Trainings & Seminars for all Industries
Organization Type
Organization/Company
WebinarCategory
Both (Technical & Non Technical)
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Accounting/Financial/Banking/Insurance

Manufacturing

Medical/Healthcare/Hospital

Food Processing

Location
Fremont, California, United States

Overview:

It is essential for industry to employ efficient and accurate

strategies for monitoring outsourced projects to minimize the

chances of receiving warning letters from competent authorities.

Companies should have robust structures in place for successful

vendor selection, contract design, and quality monitoring and risk

minimization when outsourcing activities in GXP areas to remain

compliant.

Areas Covered in the Session:
Discover Tools and Processes to Manage CROs/other Vendors
Gain an insight for CROs/other Vendors of what Sponsors Expect
and how to Meet their Expectations
Measuring CRO Performance including Metrics and Key Performance
Indicators
Managing and avoiding common pitfalls with CROs/Vendors

Who Will Benefit:
Vendor Management
Global QA/Compliance
Contracts and Outsourcing
Outsourcing Department Staff

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. Dr. Brown has 20 years
experience running clinical trials and clinical quality assurance in
the pharmaceutical industry, and auditing clinical trials
internationally.

Event Fee: One Dial-in One Attendee Price: US$150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]

Registration Fees
Available
Registration Fees Details
One Dial-in One Attendee Price: $150.00
Registration Ways
Email
Phone
Website
Address/Venue
  Online  Pin/Zip Code : 94539
Official Email ID
Contact
Event Manager

Online

[email protected]

     +1-800-447-9407
   Fax No: 302-288-6884