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2018 - How an Organization can remain Compliant with these Regulations

Date2018-06-11

Deadline2018-06-08

VenueFremont, USA - United States USA - United States

KeywordsManufacturing; Quality Assurance; Pharmaceutical products

Websitehttp://www.compliance4all.com/control/w_...

Topics/Call fo Papers

Overview:
Among those educational requirements are a course in
Introductory GMP upon employment at a pharmaceutical company,
and annual refresher GMP training.
Why should you Attend:
The laws that govern Good Manufacturing Practices (GMP) are a
cornerstone of pharmaceutical production. Still, many companies
fall short of the requirements that are written into US, UK,
European and other laws, which can have disastrous consequences
for patient health and a company's reputation, not to mention the
resultant losses in revenue due to fines, declining sales and
withdrawal of products from the market.
Areas Covered in the Session:
Food and drug oversight
Pivotal events that shaped laws in US and scope of FDA actions
Consequences of noncompliance
Building a culture of compliance
Who Will Benefit:
This course will be of benefit to anyone whose responsibilities fall
under the umbrella of manufacturing, packaging or distribution of
pharmaceutical products
Speaker Profile:
Michael Esposito has over 30 years experience in the
pharmaceutical industry and 17 years experience in GMP training
and document management. He has worked for Wyeth
Pharmaceuticals, Pfizer and Johnson & Johnson's McNeil Consumer
Healthcare Division in a variety of areas including Packaging,
project administration, Quality Assurance, Government Contracts,
translations, systems training, and international operations.
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support-AT-compliance4All.com

Last modified: 2018-04-20 15:54:02