When Conducting cGMP Regulatory Inspections 2019

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Category Educational webinars, Healthcare webinars, Biopharmaceutical, Laboratory Managers, pharmaceutical trainings

Deadline: June 05, 2019 | Date: June 07, 2019

Venue/Country: Online, U.S.A

Updated: 2019-04-22 16:14:29 (GMT+9)

Call For Papers - CFP

Yet GMPs have been enshrined into law for many countries and a drug/biologic/medical device manufacturer should have a reasonable expectation of all inspections being the same.

Why should you Attend:

This webinar will cover the key areas of how ICH Q7 was established, it's goals and objectives, expectations of the healthcare authorities involved and practical differences that you will experience in a GMP inspection of a facility by FDA, an EU Competent Authority or PMDA.

Areas Covered in the Session:

Where Inconsistencies Become a Problem: WHO, ICH, Countries

Discrepancies in global expectations

Alignment issues

Key Chapter Reviews

ICH GMP organization

Category reviews

Who Will Benefit:

Quality Assurance

Senior management

Project Managers

Qualified Persons (QPs)

Regulatory Compliance

Speaker Profile:

Angela Bazigos is the CEO of Touchstone Technologies Inc. She has degrees in Microbiology and Computing and 40 years of experience in the Life Sciences, Healthcare & Public Health Services.

Event Fee: One Dial-in One Attendee Price: $290.00

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: compliance4all14gmail.com