How an Organization can remain Compliant with these Regulations

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Category Good Manufacturing Practices, Manufacturing, gmp manufacturing, gmp good manufacturing practice, gmp in pharmaceutical industry, good manufacturing process

Deadline: June 09, 2018 | Date: June 10, 2018

Venue/Country: Online, U.S.A

Updated: 2018-04-18 15:34:18 (GMT+9)

Call For Papers - CFP

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: supportcompliance4All.com