Science Researcher Update: Spotlight on Meetings, Conferences, and Events

Webinar On Process Capability vs Process Performance - Understanding the Practical Difference

 
Seminar - Online
 
The most common method for a customer to communicate quality requirements to a supplier is through the use of a capability index.
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Tags: July, Webinar, 2015, Seminar, Biologics

Webinar on Pharmaceutical Quality Management System - Applying the Principles of Lean Documents & Lean Configuration

 
Seminar - Online
 
The Theory of Lean Documents is the product of applying lean principles to the Quality Management System (QMS) documents typically found in regulated industries.
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Tags: July, Webinar, pharmaceutical, 2015, Seminar, Biologics

Webinar on FDA Audit Practices and the 10 Most Common Cited GMP Deficiencies

 
Seminar - Online
 
The success of an audit by federal regulators does not always depend on the level of training provided to staff and department employees, but also in understanding the focus of recent inspections within the industry.
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Tags: July, Webinar, Quality Control, 2015, Seminar

Webinar on Best Practices for Communicating & Interacting with FDA Reviewers

 
Seminar - Online
 
This seminar (webinar) is intended to help those in pharmaceutical and medical device industry involved in interacting and communicating with the health authorities.
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Tags: July, Webinar, 2015, Seminar, Biologics

Webinar on Validation of Analytical Methods according to the New FDA Guidance

 
Seminar - Online
 
Recently the FDA has released a new comprehensive guidance for validation of analytical methods.
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Tags: July, Webinar, 2015, Seminar, Biologics

Webinar on FDA’s New eMDR Requirements

 
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

Pharmacovigilance Inspections & Audit Readiness Masterclass

 
Seminar - Frankfurt, Germany
 
“Helping you prepare on your journey to compliance and inspection readiness"
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Tags: Pharmacology, September, germany, 2015, Frankfurt, Seminar, Life Sciences

9th International Seminar - The Importance of All Senior Management Roles in FDA Compliance

 
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

Webinar on Developing a Quality Management System

 
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

Webinar on OSHA and the Medical Practice

 
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

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