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Colloquium Biotechnology : Tougher Import Rules for FDA Imports in 2018
Description: FDA and the Customs and Border Patrol Service (CBP) have become increasingly sophisticated and equally demanding in the submission of import information and adherence to government proce...
Concerned sectors: Biomedical -Biotechnology -
Colloquium Biotechnology : Compliant with 21 CFR Part 11, data integrity, SaaS/Cloud, and EU GDPR
Description: • This highly interactive two-day course uses real life examples and explores proven techniques for reducing costs, usually by two-thirds, associated with implementing, and maintain...
Concerned sectors: Biotechnology -Public Health -
Colloquium Biotechnology : Moving From An Operational Manager to A Strategic Leader
Description: Gain the insights and skills to know where your business stands today and where it's heading tomorrow. In today's unpredictable business environment, strategic leadership is not...
Concerned sectors: Biotechnology -Public Health -
Colloquium Biotechnology : Excel Spreadsheet Validation 2018 Tools and Techniques
Description: Spreadsheets such as Excel, are available for creating a wide range of end user applications, including widespread use in the laboratory, creating customized statistical analyses, the cr...
Concerned sectors: Biotechnology -Medical Informatics -
Conference / Seminar Biotechnology : Introduction to Adaptive Design for Clinical Trials
Description: This 2-day seminar includes an overview of Adaptive Design, and an emphasis in group sequential design, sample size re-estimation, and Phase II/III Adaptive Seamless Designs. The role o...
Concerned sectors: Biotechnology -
Conference / Seminar Biotechnology : HIPAA Compliance - Clear, Complete, Step-by-Step
Description: Organizations of all types and sizes continue to struggle needlessly with HIPAA Compliance. For example, HIPAA Risk Analysis – Risk Management is the basis of the HIPAA Compliance ...
Concerned sectors: Biomedical -Biotechnology -
Conference / Seminar Biotechnology : Quality by Design - Essential Techniques for Medical Devices
Description: Design Controls are essential for producing safe and effective medical devices. And Design Controls are considered a critical process by the FDA. Yet, Design Controls are still one of th...
Concerned sectors: Biotechnology -Medical Equipment -
Online Conference Nursing : OSHA Recordkeeping and Surviving an OSHA Audit
Description: The Occupational Safety and Health Administration (OSHA) has jurisdiction to protect the workers of America and its territories from harmful working conditions. They are a department und...
Concerned sectors: Biotechnology -Nursing -
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BIOTECHNOLOGY ARCHIVES : PAST MEDICAL EVENTS, CONGRESSES,...
Congress Acupuncture : journee apte journes des techniciens en neurophysiologie et sommeil
journnes sur les techniques eletrophysiologiques et le sommeil...
Online Conference Biotechnology : Advanced PowerPoint Tips and Tricks 2018
Overview: This webinar will show you the basics of getting started with PowerPoint, and how to start to build impactful presentations. You will learn how to build a presentation from scratch, h...
Online Conference Biotechnology : Controlling Human Error in the Manufacturing Floor (New 2018)
Overview: This course offers practical approaches and models to address human performance issues in GMP related environments by using a specific methodology to correct, prevent and avoid re-occurrenc...
Online Conference Biotechnology : Assessing and Planning for Risk (Latest 2018)
Overview: Project risk is greater the longer your project lasts, the longer the time between preparing your project plan and starting the work, the less experience you, your team members, or your org...
Online Conference Biotechnology : FDA continues to enforce through its new 21 CFR Part 11 inspection
Overview: The webinar will have the answers. In addition, using industry proven case studies on how to avoid 483 inspectional observations and warning letters attendees will learn how to prepare thei...
Online Conference Biotechnology : Quality Agreements Made Easy (Advanced 2018)
Overview: The requirements for the assurance of quality within networks and circles of entities whose responsibilities are increasing specialized present an especially vexing challenge to the managem...
Online Conference Biotechnology : cGMPs in the Quality Control Laboratory (Medical 2018)
Overview: In this webinar we will apply one aspect of this proactive approach, the review regulatory requirements and analysis of 483 and Warning Letter observations to determine if similar observati...
Online Conference Biotechnology : Risk Control According to (GxP-GMP) Requirements
Overview:  GxP/GMP regulations are required to be used in regulated industries such as food and beverages, pharmaceutical, medical devices, and cosmetics. Documentation is a critical tool for...
Online Conference Biotechnology : Highlights of FDA GLP Regulations and the (Roles) and Responsibilities
Overview:  This 3 hour GLP virtual seminar will discuss various GLP regulations (FDA/OECD GLP's) along with highlighting roles and responsibilities of management and key personnel involved i...
Online Conference Biotechnology : Best Practices for Foundational (Employee) Success 2018
Overview: FDA expectations provide some of the framework regarding types and frequency of training, there are decisions that the company will need to make in light of its evaluation of how to best ac...
Online Conference Biotechnology : Compliance for Electronic Records and Signatures (21 CFR Part 11)
Overview: Learn exactly what is needed to be compliant for all three primary areas: SOPs for the IT infrastructure, industry standards for software product features, and the 10-step risk-based valida...
Online Conference Biotechnology : FDA During New (Drug) Development 2018
Overview:  Why is it important to engage with the FDA? To discuss your development plan to support NDA or BLA regulatory submission To identify and mitigate potential issues early To identi...
Colloquium Medical Informatics : 21 CFR Part 11 compliance for software validation and SaaS/Cloud Seminar 2018
Course "21 CFR Part 11 compliance for software validation and SaaS/Cloud" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon ...
Online Conference Biotechnology : What is the Regulatory Structure in Japan 2018
Overview: This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Japan. ...

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