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Posted: 04/29/2016

Genome Editing Standards Workshop

The National Institute of Standards and Technology (NIST) will host a special workshop in partnership with the American Society of Gene and Cell Therapy (ASGCT) to discuss the standardization of measurements for the genome ed ...read more


Posted: 04/29/2016

Acoustical Society of America Spring 2016 Meeting

The Acoustical Society of America's Spring 2016 Meeting ...read more


Posted: 06/10/2016

Webinar On Basic Requirements for IQ, OQ and PQ Quality Protocols

This webinar will highlight the importance of establishing specifications, proper documentation with regards to results obtained, how to address deviations encountered and how best to summarize results obtained. Any equipment, sy ...read more


Posted: 07/12/2016

Webinar on Project Management for Non-Project Managers - Webinar Series

Today more than ever before the job titles that we hold are not entirely reflective of the work that we do. Global teams and collaboration often place those in positions of team leadership that have the least foundation to manage ...read more


Posted: 07/12/2016

Webinar on Labeling - General and Special Medical Devices Requirements

The FDA holds you strictly liable for all labeling requirements in terms of what it says, represents or implies and even how you manage your labeling with the public. If you have a labeling problem, the FDA will say that your prod ...read more


Posted: 07/12/2016

Webinar on Raw Materials Risk Management in cGMP Facilities

This webinar will guide you on how to develop, use and document Raw Materials Risk Management based on a Product Hazard Analysis and the Product Risk Management File and Report per ISO 14971 and ICH Q9. This webinar will addres ...read more


Posted: 07/12/2016

Webinar on Chief Compliance Officer: What does it take to do the job?

Description : This training will provide valuable knowledge on what companies need to do to select an "effective" Compliance Officer who will lead the organization to conceiving, developing and implementing successful GRC progra ...read more


Posted: 07/12/2016

Webinar on Investigating Deviations - Best Practices

Description : This webinar will help attendees understand the fundamental steps of a deviation investigation with focus on using facts and objective evidence to arrive at root cause and CAPA. This webinar will focus on how to av ...read more


Posted: 07/12/2016

Webinar on FDA Compliance and Laboratory Computer System Validation

Description : You should attend this seminar if you are responsible for planning, executing or managing the validation of laboratory computer systems governed by FDA regulations. Effective and compliant computer system validati ...read more


Posted: 07/12/2016

Webinar on Risk Analysis - Tools, Techniques and the New ISO Requirements

Risk is made up of two parts: the probability of something going wrong, and the negative consequences if it does. Risk can be hard to spot, let alone prepare for and manage. If you're hit by a consequence that you hadn't planned f ...read more


Posted: 07/12/2016

Webinar on Implementing Best Practices for Global Regulatory Intelligence Programs

This seminar is intended to discuss the best practices for implementing Global Regulatory Intelligence (GRI) programs including dos and don?ts. This seminar is further intended to discuss how to implement a holistic global regulat ...read more


Posted: 07/12/2016

Webinar on FDA and EU Medical Device Submissions

Description : The basic requirements for medical device regulatory submissions are essentially the same between the FDA and EU while the individual country and region requirements for submission are somewhat different. It is im ...read more


Posted: 07/12/2016

Webinar on Opioid and Pain Management: FDA Perspectives and Requirements

This seminar is intended to help industry and professionals to better understand FDA roles and regulation governing controlled substances (opioids) used for pain management. This seminar is also intended to help industry get bette ...read more


Posted: 07/12/2016

Webinar on Test Methods and Standards for Design Verification & Validation

Description : Design Control is an integral part of any quality system in regulated industries. FDA Quality System regulation, Quality System Inspection Techniques (QSR and QSIT) and ISO 13485: 2016 have specific product verific ...read more


Posted: 07/12/2016

Webinar on ASQ Certified Quality Engineer (CQE) Exam Preparatory Course - Webinar Series

The bulleted items below each webinar title represent the key topics covered during each webinar but are not meant to be exhaustive of all the topics covered. Below each webinar title is indicated the section(s) of the ASQ CQE bod ...read more


Posted: 07/12/2016

Webinar on How to Detect Lack of Data Integrity

Description : Data are central to the development, manufacture and marketing of pharmaceuticals of all types. The renewed interest in data integrity raises questions regarding what is data integrity and how to assess it. Lack of ...read more


Posted: 07/12/2016

Webinar on ISO 13485:2016 - Understanding the Changes And Requirements

This webinar is intended to help you get familiar with the changes in the recent 2016 March version of ISO 13485 including differences with ISO 13485:2003. This webinar will help you better understand, increase your awareness an ...read more


Posted: 07/12/2016

Webinar on Supply Chain Issues (21 CFR Part 820.50 and 820.80) and Warning Letters

This presentation is primarily directed to medical device quality personnel and other staff who are selecting, auditing and receiving purchased components and services (design control, quality, purchasing, and internal auditors). ...read more


Posted: 07/12/2016

Webinar on Normality Tests and Normality Transformations

This webinar explains what it means to be ?normally distributed?, how to assess normality, how to test for normality, and how to transform non-normal data into normal data. Normality Tests and normality transformations are a comb ...read more


Posted: 07/12/2016

Glass Delamination Analysis of Pharmaceutical Vials

Delamination of Type 1 pharmaceutical vials has resulted in an increasing number of recalls over the past several years. The factors leading to surface attack due to the interaction between the drug product and glass surface of fi ...read more


Posted: 06/30/2016

Life Science Vendor Table Top Show

Don't miss our Winnipeg Series! These shows provide the opportunity for life science vendors and service providers to effectively address any challenges researchers may be dealing with in the lab, as well as share the latest trend ...read more


Posted: 08/08/2016

2 Day In-Person Seminar by Ex-FDA Official on Pharmaceutical cGMP, Data Integrity and FDA Inspections ? Current Challenges and Preparations

COURSE DESCRIPTION What are the Current Good Manufacturing Practice regulations (cGMP) for Finished Pharmaceuticals (cGMP)? Why is it required to follow these regulations? This seminar will provide a review of cGMP regulations ...read more


Posted: 08/08/2016

Usa 2016 webinar on Sanitation Chemical Testing - Best Practices

Overview: Companies must provide effective Food Safety training for all employees including managers, supervisors, sanitation employees and production employees in order to produce a safe quality food product. The objective ...read more


Posted: 08/08/2016

Usa 2016 webinar on Latest FDA Update and Expectations

Overview: The Food and Drug Administration Modernization Act (FDAMA) requires that manufacturers track certain devices when the agency orders them to do so. Tracking is intended to facilitate notification and recall in the e ...read more


Posted: 08/08/2016

Usa 2016 webinar on Water System Biofilm Control and Microbial Monitoring Myths

Overview: It is an unfortunate fact that most water systems today have been designed and are operated and controlled using at least some traditional concepts and methods that are downright wrong. So how could such traditions be ...read more


Posted: 08/08/2016

Usa 2016 webinar on The Achilles Heel of cGMP Compliance

Overview: The last few years have seen an increase in product recalls. For this and other reasons, the U.S. FDA come under increasing negative public scrutiny. High profile drug recalls, food chain problems and contamination ...read more


Posted: 08/08/2016

Usa 2016 webinar on Avoiding Pitfalls With Spray Foam Insulation

Overview: The use of spray polyurethane foam insulation in building construction has increased dramatically over the past decade because of its superior insulating qualities, performance and ability to provide all four barrier ...read more


Posted: 08/06/2016

INTRODUCTION TO MOLD INVESTIGATION & REMEDIATION CLASS

Learn How to Safely Investigate and Evaluate Mold and Moisture in Homes and Buildings. Investigating, evaluating and remediation of moisture and mold affected materials in buildings can be complicated. Join Us! INTRODU ...read more


Posted: 09/12/2016

GMP requirements for quality control and contract laboratories 2016

Overview: Quality control and related contract laboratories are considered at high risk because after testing and approval, drug products and Active Pharmaceutical Ingredients (APIs) are released to the market without further ch ...read more


Posted: 09/17/2016

American Association of Parmaceutical Scientists Annual Meeting & Exposition

Join us for an innovative program including: Resources?the top scientists, CROs and CMOs in the world will be at AAPS. Research partner?check the sessions and posters to see who is making advances in your field. Suppliers wit ...read more


Posted: 09/24/2016

Webinar on optimizing cell therapy manufacturing through custom, single-use solutions

Live Tuesday 11th October 2016, and available to view on demand after the live event. Join us for this engaging webinar to see how custom, single-use solutions can be used to close up process steps in the manufacturing of cell the ...read more


Posted: 09/24/2016

Case Studies: Scaling Cell Therapy Manufacturing Webinar

Live Tuesday 27th September 2016. Gain insights into T-cell expansion, viral vector production and scaling production of mesenchymal stem cells (MSCs) through the use of a functionally closed, automated, cell culture process. G ...read more


Posted: 11/07/2016

TAKING COUNTERFEITS OFFLINE: EXPLORING TECHNOLOGY OPTIONS FOR TOY COMPANIES

This 60-minute webinar will provide TIA members and other stakeholders with information regarding a newly available online brand protection tool that facilitates the monitoring and takedown of counterfeit goods in the marketplace, ...read more


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