San Francisco Professional Events List

  • Tougher Import Rules for FDA Imports in 2018

    Background: FDA and the Customs and Border Patrol Service (CBP) have become increasingly sophisticated and equally demanding in the submission of import information and...

    15 Feb 9:00 AM
  • Risk Management in Medical Devices Industry

    Gaps, incorrect or incomplete implementation of software can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively...

    15 Feb 9:00 AM
  • Project Management for Non-Project Managers

    This two-day seminar will begin by laying the foundation for the subject by first defining what a project is and then discussing the unique roles that the project manager must...

    20 Feb 9:00 AM
  • Enzymes in Drug Discovery Summit (gtc)

    Description GTCbio conferences aim to facilitate transformational platforms that would have a significant impact on scientific research, drug development and healthcare....

    22 Feb 8:00 AM
  • Essentials Of USP Microbiology - USP General and Information Microbiology...

    Description Essentials Of USP Microbiology - Reading Between the Lines of the USP General and Information Microbiology Chapters *** LIMITED TIME OFFER: FREE $100 AMAZON GIFT...

    22 Feb 8:30 AM
  • REACH and RoHS Compliance: Gain a Deeper Understanding (com) A

    Description REACH and RoHS Compliance: Gain a Deeper Understanding *** LIMITED TIME OFFER: FREE $100 AMAZON GIFT CARD! *** REGISTER TODAY! This 2 day seminar will go into the...

    22 Feb 8:30 AM
  • A Risk Based Approach To Data Integrity (ntz)

    Description *** LIMITED TIME OFFER: FREE $100 AMAZON GIFT CARD! *** REGISTER TODAY! The impact of Data Integrity issues on a regulated company can be significant: it can result...

    22 Feb 9:00 AM
  • Evolution of the Quality Management System - How to go from Surviving to Thriving

    Using lecture, discussion, and exercises, this 2 day seminar will focus on taking your QMS from surviving to thriving. We'll move from understanding the regulatory requirements,...

    22 Feb 9:00 AM
  • Evolution of the Quality Management System - How to go from Surviving to Thriving

    Using lecture, discussion, and exercises, this 2 day seminar will focus on taking your QMS from surviving to thriving. We'll move from understanding the regulatory requirements,...

    22 Feb 9:00 AM
  • The Value of a Human Factors Program

    This seminar will explain the implementation of ISO 62366 and the regulatory expectations discussed in the 2016 FDA Guidance for a compliant human factors/ usability program....

    22 Feb 9:00 AM
  • Good Clinical Data Management Practices (GCDMP)

    Why should you attend: Good clinical data management (CDM) is paramount for a successful research. After all, Garbage In, Garbage Out (GIGO). CDM is involved in all aspects of...

    22 Feb 9:00 AM
  • A Risk Based Approach To Data Integrity

    The impact of Data Integrity issues on a regulated company can be significant: it can result in recalls of products, warning or untitled letters, import alerts, injunctions,...

    22 Feb 9:00 AM
  • The Value of a Human Factors Program

    This seminar will explain the implementation of ISO 62366 and the regulatory expectations discussed in the 2016 FDA Guidance for a compliant human factors/ usability program....

    22 Feb 9:00 AM
  • HIPAA Compliance 2018

    This two day seminar takes the participants through HIPAA compliance from start to compliance. The first presentation explains the history of HIPAA, why it came to being and its...

    26 Feb 9:00 AM
  • Validation and 21 CFR Part 11 Compliance of Computer Systems

    Computer Systems Validation (CSV) also known as Software Validation is all-pervasive in the Life Sciences Industry. It is a requirement of all the predicate rules, as well as 21...

    01 Mar 9:00 AM
  • Biostatistics for the Non-Statistician

    Why should you attend: Statistics is a useful decision making tool in the clinical research arena. When working in a field where a p-value can determine the next steps on...

    01 Mar 9:00 AM
  • ISO 13485:2016 Implementation Workshop

    The medical device industry is in the midst of major change, with the publication of the FDA's UDI Regulation, the first revision to the ISO Quality Management Systems standard...

    01 Mar 9:00 AM
  • The A to Z's of Microbial Control, Monitoring and Validation of Water Syste...

    Description The A to Z's of Microbial Control, Monitoring and Validation of Water Systems for Pharmaceuticals, Biologics, Medical Devices, Cosmetics, and Personal Care Products...

    08 Mar 8:30 AM
  • Regulatory Requirements and Principles for Cleaning Validation

    This 2 day course will cover practical guidance on cleaning validation regulatory compliance, in conjunction with, risk-based, reasonable and informed decision making and...

    08 Mar 9:00 AM
  • HIPAA Compliance 2018

    This two day seminar takes the participants through HIPAA compliance from start to compliance. The first presentation explains the history of HIPAA, why it came to being and its...

    08 Mar 9:00 AM
  • Cannabis Partnerships (exl) S

    Description The Cannabis Partnerships Congress The Cannabis Partnerships Congress is a multi-track approach to bringing the stakeholders involved in the cannabis-based...

    12 Mar 8:00 AM
  • Supplier Management for Medical Device Manufacturers

    Supplier selection and management is one of the critical issues for medical device manufacturers. Suppliers provide materials and services to the device manufacturer, which...

    12 Mar 9:00 AM
  • 21 CFR Part 11 compliance for software validation and SaaS/Cloud

    This interactive two-day course explores proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments....

    14 Mar 8:30 AM
  • Supplier Management for Medical Device Manufacturers

    Supplier selection and management is one of the critical issues for medical device manufacturers. Suppliers provide materials and services to the device manufacturer, which...

    15 Mar 9:00 AM
  • A Risk Based Approach To IT Infrastructure Qualification & Compliance

    GxP Regulated companies are dependent on validated GxP computerized applications to conduct their day to day operations. These applications are, in turn, depended upon a...

    15 Mar 9:00 AM
  • Verification vs. Validation - Product Process Software and QMS

    This course will review the company Master Validation Plan for major key inputs and CGMP deficiencies. It will address the FDA's newer and tougher regulatory stance. This...

    15 Mar 9:00 AM
  • International Coffee Festival

    The International Coffee Festival aims to brings coffee lovers and coffee producers together in an all inclusive event. The event includes a barista championship, late night...

    16 Mar 10:00 AM
  • Combination Products

    This seminar provides Professionals working in this area with: A thorough understanding of the complexities involved Covers all the relevant regulations and guidelines Gives...

    19 Mar 9:00 AM
  • Ocular Diseases Drug Discovery (gtc)

    Description The 10th Ocular Diseases Drug Discovery Conference is taking place on March 20-21, 2018 in San Diego, CA. We are excited to have top representatives from the...

    20 Mar 8:00 AM
  • The New EU Medical Device regulation

    Regulation proposals of the European Commission Background In 2012, the Commission adopted a package of measures on innovation in health. The package consisted of a...

    22 Mar 9:00 AM
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