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Activity Provided By:

CfPA

Sterile Products: Formulation, Manufacture and Quality Assurance

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Overview / Abstract:

Who Should Attend?
This intensive course is intended for those having specific responsibilities in the areas of sterile drug product science and technology. It will be of particular value to those in:

• Research
• Development
• Production
• Quality Assurance and Control

Those who wish to broaden their appreciation of these technologies and review the latest developments, as well as managers who have responsibility for a broader base of activities will find the course of interest.

Course Description
This comprehensive course provides an appreciation and general understanding of the overall contemporary state of science and technology associated with the design, development and manufacturing of sterile drug dosage forms. Emphasis will be oriented toward formulation development and product manufacture of quality sterile dosage forms that meet or exceed expected good manufacturing practice requirements.

Expiration

May 17, 2018

Discipline(s)

Education (Higher Ed)

Format

Live / Seminar, Seminar

Cost

$2850

Credits / Hours

1.8 CEUs

Accreditation

IACET, ASQ

Is This Activity Certified for "Live" Credit?

YES

Presenters / Authors / Faculty

Dr. Gregory A. Sacha; Senior Research Scientist

Keywords / Search Terms

CfPA Sterile Products, Formulation, Manufacture, Quality Assurance, formulation, sterile dosage forms, good manufacturing practice, Research, Development, Production, Quality Assurance and Control Live CE CME Seminar CE CME

LIVE Activity Location Details

Date(s)
05-16-2018 - 05-18-2018

Amsterdam, The Netherlands
 
Netherlands

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