Seminar - Online
Recently the FDA has released a new comprehensive guidance for validation of analytical methods.
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Science Researcher Update: Spotlight on Meetings, Conferences, and Events
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Seminar - Online
Manufacturers and importers must report adverse events associated with a risk to health or death. Until now, the reports were submitted in hardcopy using MedWatch form 3500A.
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Tags: Medical Device Technology, July, Webinar, 2015, Seminar
Seminar - Princeton, NJ, United States
The goal of this seminar is to familiarize senior executives and high level managers from every department in a regulated firm, with their personal responsibility in assuring your firm of the highest level of FDA Compliance.
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Tags: July, Webinar, Development, Princeton, NJ, 2015, Seminar
Seminar - Online
This webinar provides an overview of the Quality Management System requirements. We will discuss ISO Quality Management standards and the FDA Quality System requirements.
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Tags: Medical Device Technology, July, Webinar, Quality Control, 2015, Seminar
Seminar - Online
This webinar will be addressing OSHA and the medical practice. It will address risk factors in terms of an OSHA audit, blood borne pathogens, and HAZCOM, universal precautions, etc.
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Tags: July, Healthcare, Webinar, 2015, Seminar
Seminar - Online
Many laboratories are unsure about which QC practices are needed to assess media performance to meet not only their requirements, but also the requirements of ISO/IEC 17025: 2005.
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Tags: July, Webinar, Quality Control, pharmaceutical, 2015, Life Sciences
Seminar - Online
Within the Pharmaceutical Industry, the changeover from one product to another on a filling/packaging line, although relatively a simple concept, has significant implications from a regulatory standpoint if cross-contamination is permitted to occur.
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Tags: July, Webinar, pharmaceutical, 2015, Seminar, 1 day only, Biologics
Spotlight on Science Meetings, Conferences and Events brings you information on the following event: Webinar: Best Practices for Communicating and Interacting with FDA Reviewers
This seminar (webinar) is intended to help those in pharmaceutical and medical device industry involved in interacting and communicating with the health authorities. In particular, this seminar will discuss best practices for communicating, interacting and negotiating with FDA reviewers before and during the review process.
The speaker will guide you through the details of what is best in exercising your judgment and discretion while communicating and interacting with the FDA reviewers. In this 60-min presentation, the speaker will guide you through the details of how to implement the systematic and holistic risk management for drugs, biosimilars, biologics and medical devices.
This is an online seminar.
Mississauga, Ontario
https://compliancetrainings.com
Monday, August 3, 2015
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Tags: August, Webinar, pharmaceutical, 2015, August 2015
Seminar - Online
This webinar will provide valuable assistance to all U. S. FDA-regulated companies. It will assist in their reviewing and modifying their regulatory compliance stance in view of the areas the FDA indicates are of growing / future interest / emphasis.
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Tags: June, Medical Device Technology, Webinar, pharmaceutical, 2015, Seminar, Biologics
Seminar - Online
This webinar should be "required reading" for those who want to be a member of a drug project team and any of the sub-teams.
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Tags: June, Webinar, Clinical Research, 2015, Seminar, Biologics
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