Strategies To Prevent Manufacture And Distribution Of Substandard Medications
April 10, 2019 - Fremont CA USNetzealous LLC DBA - Compliance4All
compliance4all14@gmail.com
Phone:18004479407
Fax:302-288-6884
Overview: In this webinar we will provide you with best practices that have been proven effective, and equip you with the means to advocate for these ideas within your organization. Why should you Attend: If a legitimate product is not manufactured according to quality standards or becomes degraded as it travels through its supply chain, it can be ineffective at best or deadly at worst. Examples of potential dangers that can occur include temperature excursions, inappropriate use, and unsafe ingredients inadvertently added to the product. Areas Covered in the Session: Solutions Maintain a robust quality system Supplier quality Product testing Monitoring temperature Who Will Benefit: Pharmaceutical Industry Supply Chain Quality Assurance Packaging and Labeling Manufacturing Warehousing and Distribution 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: compliance4all14@gmail.com