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Good Documentation Guideline (Chapter 1029 USP)

June 10 @ 10:00 am - 11:00 am CDT

$150.00

Overview:
This 60-min webinar will familiarize participants with USP Chapter
<1029> on good documentation guidelines. This session will wrap
up the general concept and will provide information as to what
needs to be documented in certain records.

Why should you Attend:
If you are involved in any product manufacturing, knowing GDP
regulations is a must for you. Manufacturing is prone to any kind
of errors, deviations, unforeseen events. It is of utmost importance
to know what you need to do in case of any unforeseen situations.

Areas Covered in the Session:
Laboratory records
Equipment-related documentation
Deviations and investigations
Batch records

Who Will Benefit:
Laboratory Personnel / Managers
Validation Specialists
Clinical Trial Personnel
Project Managers

Speaker Profile:
Dr. Afsaneh Motamed Khorasani ,PhD is a Medical and scientific
Affairs expert and a Senior Scientist with a strong background in
biomedical science and clinical trial/research. She has a tenured
and diverse range of experience in medical affairs, basic and
industrial clinical research and development, clinical trials, Medical
and regulatory writing and intellectual property.

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

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

Details

Date:
June 10
Time:
10:00 am - 11:00 am
Cost:
$150.00
Event Tags:
Website:
https://www.compliance4all.com/control/w_product/~product_id=502560LIVE?channel=complianceinsights_Jun_2019_SEO

Organizer

compliance4All
Phone:
18004479407
Email:
compliance4all14@gmail.com
Website:
http://www.compliance4all.com

Venue

Online Event
539 W. Commerce #1821
Dallas, TX 75208 United States
+ Google Map
Phone:
1-(214)-628-2958
Website:
https://www.trainzsmith.com/