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  • Strategies for Improving Effectiveness and Efficiency of your Quality Management System

    Strategies for Improving Effectiveness and Efficiency of your Quality Management System

    Quality Control, Safety & Security Boston (Massachusetts) July 5, 2018 1295.00 Dollar US$

    This two-day seminar will cover the essentials of an effective yet efficient Quality management system for medical device companies. An efficient and effective Quality System can be a competitive advantage for companies by leading to improved Quality...

  • Fundamentals of Statistical Design for Clinical Trials Seminar

    Fundamentals of Statistical Design for Clinical Trials Seminar

    Clinical Baltimore, MD (Maryland) July 5, 2018 1295.00 Dollar US$

    This 2-day seminar includes an overview of the need for clinical research, types of clinical trial designs, common statistical tests, considerations of sample size, and randomization techniques. The role of statistics in clinical trials incorporates ...

  • Course on GxP/GMP Regulations: Requirements Compliance 2018

    Course on GxP/GMP Regulations: Requirements Compliance 2018

    Quality Control, Safety & Security San Diego (California) March 6, 2018 1295.00 Dollar US$

    Overview: GxP/GMP regulations are required to be used in regulated industries such as food and beverages, pharmaceutical, medical devices, and cosmetics. GMP regulations describe required quality management system for production and testing of produc...

  • 16th World Medical Nanotechnology Congress 2018 (Medical Nanotechnology 2018)

    16th World Medical Nanotechnology Congress 2018 (Medical Nanotechnology 2018)

    Bioinformatics - Data Analysis Tokyo (Tokyo) April 6, 2018 699.00 Dollar US$

    Medical Nanotechnology 2018 is hosted by Conference Series llc LTD . This event brings together leading scientists, engineers, doctors, directors of companies, Researchers from Material science, pharmaceuticals, Biomedical Engineering, Medicine and P...

  • Validation and 21 CFR Part 11 Compliance of Computer Systems

    Validation and 21 CFR Part 11 Compliance of Computer Systems

    Data Management Fremont (California) July 3, 2019 545.00 Dollar US$

    This course is appropriate for beginner and experienced person alike. The topics will build on each other and will give you the latest trends in our heavily regulated industry and how to make it easy for yourself while still achieving data integrity....

  • Texting and E-mail with Patients - Meeting Patient Requests within the HIPAA Rules

    Texting and E-mail with Patients - Meeting Patient Requests within the HIPAA Rules

    Training and Teaching Fremont (California) July 3, 2019 545.00 Dollar US$

    E-mail has long been a staple of people's lives, but as we move into the new digital age, it seems everyone is moving to a new smart phone and wants to use it in all the incredible ways it can be used for health care purposes, including the use of e-...

  • 6-Hour Virtual Seminar on Clinical Data Management - Part II

    6-Hour Virtual Seminar on Clinical Data Management - Part II

    Quality Control, Safety & Security Fremont (California) July 3, 2019 545.00 Dollar US$

    When new drugs or devices are tested in humans, the data generated by, and related to, these trials are known as clinical data. This data represents a huge investment by the biopharmaceutical or device company and is one of its greatest assets. It is...

  • The EU Clinical Trial Regulation - EU Filings & Registrations

    The EU Clinical Trial Regulation - EU Filings & Registrations

    Quality Control, Safety & Security Fremont (California) July 3, 2019 545.00 Dollar US$

    This course covers the requirements for conducting Clinical Studies across the EU via the requirements of the EU Clinical Trial Regulation (for Drugs & Biologics). The course also covers recent updates on EU-GCP associated with the new regulatory...

  • 6-Hour Virtual Seminar on Tougher Import Rules for FDA Imports in 2019

    6-Hour Virtual Seminar on Tougher Import Rules for FDA Imports in 2019

    Data Management Fremont (California) July 3, 2019 545.00 Dollar US$

    Importing FDA regulated products requires careful planning before you even start. Registration, product compliance, record and data submission must be exactly correct or your product will be detained. Likewise, the U.S. Customs and Border Protection ...

  • 6-Hour Virtual Seminar on Batch Record Review and Product Release

    6-Hour Virtual Seminar on Batch Record Review and Product Release

    Drug Development Fremont (California) July 3, 2019 545.00 Dollar US$

    Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records. Additionally, there must be written procedures for a batch record review process that demonstrate c...

  • 21 CFR Part 11 Compliance for Computer Systems Regulated by FDA

    21 CFR Part 11 Compliance for Computer Systems Regulated by FDA

    Training and Teaching Fremont (California) July 3, 2019 545.00 Dollar US$

    The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11. This includes development of a company philosophy and ...

  • HIPAA 2019 - Staying Competitive and Complying with HIPAA

    HIPAA 2019 - Staying Competitive and Complying with HIPAA

    Bioinformatics - Data Analysis Fremont (California) January 21, 2019 545.00 Dollar US$

    This seminar will demonstrate how Covered Entities and Business Associates can comply calmly, confidently and completely with the HIPAA Rules. The secret is - HIPAA Rules are easy and routine to follow - when you know the steps. Paul Hales will captu...