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Event Type: Web Based Seminar |
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Title: Understanding CFR part 210-211 Requirements for Drug Products |
 Register Online |
Description: This is a basic overview of CGMP’s with a cursory review of CFR parts 210-211. |
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Date: 10:00 a.m. – 11:00 a.m. PST. June 24, 2008. |
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Location: Online |
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Event Type: Web Based Seminar |
View Brochure |
Title: Roles and Responsibilities of Quality Assurance for Pharmaceutical Products |
Register Online |
Description: Detailed review of QA roles and responsibilities as defined by CFR 210-211, ICH Q7A and EU Guidelines to Good Manufacturing Practices. |
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Date: 10:00 a.m. – 11:00 a.m. PST. July 23, 2008. |
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Location: Online |
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Event Type: Web Based Seminar |
View Brochure |
Title: Validation Requirements Based on ICH Q9 “Quality Risk Management" |
Register Online |
Description: Review principles and examples of tools for quality risk management for the purpose of pharmaceutical manufacturing and process validation. |
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Date: 10:00 a.m. – 11:00 a.m. PST. July 24, 2008. |
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Location: Online |
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Event Type: Web Based Seminar |
View Brochure |
Title: Vendor/Supplier Qualification |
Register Online |
Description: An overview of the requirements for vendor and supplier qualification and how to develop a comprehensive qualification program. |
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Date: 10:00 a.m. – 11:00 a.m. PST. August 13, 2008. |
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Location: Online |
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Event Type: Web Based Seminar |
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Title: Understanding Current FDA Requirements for Control of Raw Materials and Components Suppliers |
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Description: Review FDA Form 483 observations and Warning Letters to pharmaceutical and biotechnology manufacturing companies for lack of adequate controls in the evaluation of raw materials and component suppliers to ensure that these materials are acceptable for use. |
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Date: October 22, 2008, 11:00 am - 12:30 pm PST |
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Location: Online |
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Event Type: Web Based Seminar |
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Title: FDA Regulations Pertaining to Implementation of Clinical Trials |
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Description: A detailed review of FDA regulations for Clinical Trials Process. After attending this session, participants will have an understanding of FDA regulations pertaining to the implementation of clinical trials and concepts of Good Clinical Practice (GCP) and Bioethics. |
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Date: October 23, 2008, 11:00 am -12:30 pm PST |
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Location: Online |
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Event Type: Web Based Seminar |
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Title: Understanding Single Sampling Attributes Acceptance Sampling for Defectives; Going beyond ANSI Z1.4 and ISO 2859 |
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Description: This training will answer all your questions about acceptance sampling for defectives. You will learn how to select the appropriate sample sizes using scientific methods and gain confidence in justifying your sampling plan. |
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Date: October 30, 2008, 11:00 am - 12:30 pm PST |
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Location: Online |
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Event Type: Training Course |
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Title: Understanding Good Clinical Practices |
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Description: One-day comprehensive training course FDA regulations pertaining to implementation of clinical trials, GCP concepts and Bioethics. |
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Date: November 5, 2008 8:00 a.m. - 5:30 p.m. |
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Location: La Costa Resort & Spa, Carlsbad, N. San Diego County |
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Event Type: Training Course |
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Title: Designing Cost-Effective Stability Programs |
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Description: This is a one day intensive training course for anyone working in the pharmaceutical or biopharmaceutical field who wants to learn how to design and implement both cost and time effective stability programs |
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Date: February 4, 2009 8:00 a.m. - 5:00 p.m. |
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Location: La Costa Resort & Spa, Carlsbad, N. San Diego County, California |
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EVENT PLANNING BY:
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