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Scientific, Technical & Laboratory
Training Courses and Conferences

Learn from scientific, technical, and lab related expositions, annual meetings, trade shows, conferences, courses, webinars, workshops, training, EXPO's and seminars. For more information on scientific, technical or lab training courses and conferences, please contact 403-770-1992 or email us .
2011 Scientific, Technical and Laboratory Training Courses and Conferences
start date
sponsor
lab training courses and conferences
location
April 2011
Advanced courses in Regulatory Affairs
Course or Conference Sponsor : Institute of Pharmaceutical Management
Institute of Pharmaceutical Management (IPM) is a Mumbai based pioneering training institute engaged in conducting industry-oriented Diploma and Post-graduate Diploma courses Read More...
Maharashtra, India
9/19/2011
3rd Annual Business of Biosimilars and Biobetters
Course or Conference Sponsor : Institute for International Research
This year, The Business of Biosimilars event is expanding to the Business of Biosimilars and Biobetters in order to better address the needs of our audience and reflect the c Read More...
MA, USA
12/13/2011
Live Web seminar on HOW TO MANAGE COMPLAINT FILES By Compliance2go
Course or Conference Sponsor : Compliance 2 go
Description This webinar provides linkage between CAPA and the complaint file. It focuses on risk assessment and impact assessment as tools for linkage between complaint ha Read More...
Houston, United States
12/13/2011
Live Web seminar on HOW TO MANAGE COMPLAINT FILES By Compliance2go
Course or Conference Sponsor : Compliance 2 go
Description This webinar provides linkage between CAPA and the complaint file. It focuses on risk assessment and impact assessment as tools for linkage between complaint ha Read More...
Houston, United States
11/15/2011
Biomarker Application for Improved Clinical Trial Outcomes
Course or Conference Sponsor : Institute for International Research
The only personalized medicine conference allowing you to make biomarkers and diagnostics available during every stage of clinical research, to stratify patients, prove clinic Read More...
MA, USA
11/09/2011
Health Insurance Exchange Congress
Course or Conference Sponsor : Institute for International Research
Welcome to the only event bringing together health plans, state governments and the federal government to address the opportunities and challenges presented by the implementat Read More...
Maryland, United States
10/20/2011
HIPAA Compliance and Patient Care: Where the Challenges are - Webinar By mentorhealth
Course or Conference Sponsor : Mentor Health
Why you should attend: Healthcare organizations have a responsibility to protect identifiable health information of patients. However, the hospitalized patient and those that Read More...
Delaware, United States
10/12/2011
3rd Annual Partnerships in Clinical Trials Asia
Course or Conference Sponsor : Institute for International Research
The largest concentration of clinical decision makers specializing in clinical development, operations and outsourcing meet to provide you the opportunity to establish benchma Read More...
, China
10/11/2011
Audits In The Health Care Industry - Getting Ready for an Outside Audit - Webinar By mentorhealth
Course or Conference Sponsor : Mentor Health
Areas Covered in the Session: Overview of audit risks 14 Strategies to tackling auditors: i.e. Appoint Audit Manager Appoint Audit Committee Proactively seek out info fro Read More...
Delaware, United States
10/03/2011
Cell Based Assays and Bioanalytical Method Development
Course or Conference Sponsor : Institute for International Research
Over the past 6 years, this meeting is the only place to find the scientists who are discovering new approaches and solutions to the assay development challenges you face ever Read More...
California, United States
09/19/2011
4th Annual Biorepositories
Course or Conference Sponsor : Institute for International Research
IIR's 4th annual Biorepositories event convenes industry innovators who recognize that a well-maintained biorepository is a significant value generator and that improvements Read More...
Massachusetts, United States
09/19/2011
15th Annual eClinical Integration Summit
Course or Conference Sponsor : Institute for International Research
The eClinical Technology Summit encompasses the next generation of clinical data management. Obtain cutting edge strategies for collecting, integrating and reporting data th Read More...
Masachusetts, United States
09/19/2011
9th Annual Central Labs
Course or Conference Sponsor : Institute for International Research
The only place to meet face to face with your core labs to improve clinical quality from protocol design through regulatory submission to keep your trial on time and on budget Read More...
MA, USA
09/19/2011
8th Annual Project & Portfolio Management for the Drug & Device Industry
Course or Conference Sponsor : Institute for International Research
Project Management for the Drug & Device Industry is a must-attend event for any project manager looking to increase the effectiveness and efficiency of clinical development p Read More...
MA, USA
09/19/2011
Cell Therapy Commercialization Summit
Course or Conference Sponsor : Cell Therapy Summit
The Cell Therapy Commercialization Summit is the only event where business executives, along with clinical operations stakeholders, learn cutting-edge strategies towards produ Read More...
MA, USA
09/15/2011
Live Webinar on Lyophilization Process Development and Cycle Design
Course or Conference Sponsor : Compliance 2 go
By taking the time to characterize the thermal This seminar will cover the process and benefits of using an empirical approach to design an optimized lyophilization cycle. In Read More...
Texas, United States
09/14/2011
16th Annual Medicaid Drug Rebate Summit
Course or Conference Sponsor : institute for International Research
For fifteen years, this event has been at the forefront of policy changes and operational compliance, bringing a unique mix of contracting and pricing specialists together wit Read More...
IL, USA
08/25/2011
The new Variations Regulation - Strategies for Grouping and Worksharing - Pharmaceutical products change over time; the drivers of changeinclude innovation, continual improvement, the output of process performanceand product quality monitoring and CAPA among others (ICH-Q10 -PharmaceuticalQuality System).  In most territoriespost approval changes must be recorded and notified to the competent authorities.  In the EU Regulations (EC)No1084/2003 and (EC)1085/2003 formed the legal basis of variations andpost-registration changes to products licensed via the Mutual Recogn
The new Variations Regulation - Strategies for Grouping and Worksharing
Course or Conference Sponsor : Michor Consulting e.U
Pharmaceutical products change over time; the drivers of changeinclude innovation, continual improvement, the output of process performanceand product quality monitoring and C Read More...
N/A - webinar, N/A - webinar
08/11/2011
Quality by Design (QbD) and Post-approval change management protocols - Quality by Design (QbD) is a concept that affects regulatory documentation andinformation provided by manufacturers to the authorities.  Recent developments in QbD have had apositive impact on life cycle management and the management of post marketinformation.  QbD can help to avoidquality issues by proper planning in the development stage leading tosimplified process development, commercialization and change management, lifecycle management and the processing of variations.  In a similar way po
Quality by Design (QbD) and Post-approval change management protocols
Course or Conference Sponsor : Michor Consulting e.U
Quality by Design (QbD) is a concept that affects regulatory documentation andinformation provided by manufacturers to the authorities. Recent developments in QbD have had ap Read More...
N/A, N/A-webinar
08/01/2011
2nd Annual Partnerships in Clinical Trials Latin America
Course or Conference Sponsor : Institute for International Research
The successful launch of Partnerships in Clinical Trials Latin America last year in Argentina drew 100+ leading pharmaceutical executives! The world's leading clinical drug de Read More...
, Brazil
07/24/2011
American Association of Clinical Chemistry AACC 2011 Annual Meeting  - Join thousands of your peers in Atlanta, Georgia - July 24-28 - for the 2011 AACC Annual Meeting and Clinical Lab Expo.  You'll be able to design an education program that suits your individual professional needs.

    * PARTICIPATE in exciting educational sessions conducted by dynamic presenters.
    * LEARN about the latest products and services available for clinical scientists.
    * INTERACT with and learn from your colleagues in an informal environment.
American Association of Clinical Chemistry AACC 2011 Annual Meeting
Course or Conference Sponsor : American Association of Clinical Chemistry AACC
Join thousands of your peers in Atlanta, Georgia - July 24-28 - for the 2011 AACC Annual Meeting and Clinical Lab Expo. You'll be able to design an education program that sui Read More...
GA, USA
07/23/2011
XXIII ISTH International Society on Thrombosis and Haemostasis Congress - It is my great pleasure to announce that the XXIII Congress of the International Society on Thrombosis and Haemostasis and 57th SSC Meeting will be held just in Kyoto for 2011...


07/29/2011
XXIII ISTH International Society on Thrombosis and Haemostasis Congress
Course or Conference Sponsor : International Society on Thrombosis and Haemostasis ISTH
It is my great pleasure to announce that the XXIII Congress of the International Society on Thrombosis and Haemostasis and 57th SSC Meeting will be held just in Kyoto for 2011 Read More...
, Japan
07/18/2011
WORLDx Congress
Course or Conference Sponsor : Institute for International Research
WORLDx Congress will offer the most up-to-date insight into new FDA strategies and highlight strategies for success in biomarker validation, partnerships formation, regulatory Read More...
Maryland, USA
07/18/2011
WORLDx Congress
Course or Conference Sponsor : Institute for International Research
WORLDx Congress will offer the most up-to-date insight into new FDA strategies and highlight strategies for success in biomarker validation, partnerships formation, regulatory Read More...
Maryland, USA
06/22/2011
What to Expect and How to Prepare for FDA Inspections - By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panel
As recent headlines demonstrate, non-compliance with US Food & Drug Administration US FDA laws and regulations could cost your firm millions. In addition to significant rev Read More...
DE, USA
06/16/2011
Introduction to Master Validation Plans - By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panel
This webinar provides an introduction to the creation, implementation, and maintenance of Validation Master Plans. Key benefits of this seminar include: Achieve sati Read More...
DE, USA
06/16/2011
Understanding and Implementing USP 1058: Analytical Instrument Qualification - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panel
Analytical instruments should be qualified to demonstrate suitability for the intended use. Despite the fact that instrument qualification is nothing new and companies spend a Read More...
DE, USA
06/16/2011
Designing an effective cleaning validation in today's regulatory environment
Course or Conference Sponsor : Compliance Online
This presentation will address the most current expectations for cleaning validations of reusable medical devices that are performed in support of the instructions in the inst Read More...
CA, USA
06/15/2011
The 510(k) Submission: Requirements, Contents, and Options - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panel
Knowing when and how to properly submit a 510(k) for a device or change to a device is critical to a company's regulatory and financial health. Your goal is to get the 510(k) Read More...
DE, USA
06/09/2011
Understanding good Closed Loop CAPA system - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : GlobalCompliance Panel
This webinar will present how organizations can pursue continual improvements and address the concerns of non-conformances and develop corrective/preventive actions to prevent Read More...
DE, USA
06/08/2011
Effective Risk Based Approach to Auditing and Qualifying Suppliers and Vendors - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panel
Overview: This webinar will demonstrate how to implement an effective audit program. Regulatory agencies hold firms responsible for delivering high quality products that meet Read More...
DE, USA
06/07/2011
Risk-Based Validation for GxP Facilities - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panel
This presentation teaches a practical methodology for creating and applying Risk-Based Equipment Validation. It shows an example of how this process may be integrated into a f Read More...
DE, USA
05/26/2011
Sterilization Options for Challenging Products
Course or Conference Sponsor : Compliance Online
This presentation will review various sterilization processes and their general compatibility to various types of challenging medical products as well as some of the challenge Read More...
CA, USA
05/24/2011
The Use and Mis-use of FMEA in Medical Device Risk Management
Course or Conference Sponsor : Compliance Online
FMEA is a tool designed for product reliability, which has been modified for use in risk management but has some pitfalls in this use. The presentation will discuss the proper Read More...
CA, USA
05/20/2011
Last changes in Canadian ethics regulations for clinical trial - This webinar presentation will help you to understand the last changes that occurred in Canadian ethics regulations.  It will clarify for sites and sponsors how to ease the ethics process and how to get more quicker ethics approval. Participant will understand how to apply the last changes in ethics regulation in the day-to-day work.

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.
Last changes in Canadian ethics regulations for clinical trial
Course or Conference Sponsor : Compliance Online
This webinar presentation will help you to understand the last changes that occurred in Canadian ethics regulations. It will clarify for sites and sponsors how to ease the et Read More...
CA, USA
05/19/2011
Recalls & Vigilance - When to Report Complaints - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panel
Overview: This webinar will acquaint one with the lessons learned from over 30 years of adverse events and complaints. FDA has issued warning letters for failing to properl Read More...
DE, USA
05/19/2011
Recalls & Vigilance - When to Report Complaints - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panel
Overview: This webinar will acquaint one with the lessons learned from over 30 years of adverse events and complaints. FDA has issued warning letters for failing to properl Read More...
DE, USA
05/17/2011
Designing a CAPA System that Meets and Exceeds Regulatory Requirements - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : global Compliance Panel
Overview: CAPA is the most audited Quality subsystem in any Quality system. Most of the warning letters written by the FDA in 2010 were CAPA relate. Avoiding FDA CAPA findings Read More...
DE, USA
05/17/2011
Designing a CAPA System that Meets and Exceeds Regulatory Requirements - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panel
Overview: CAPA is the most audited Quality subsystem in any Quality system. Most of the warning letters written by the FDA in 2010 were CAPA relate. Avoiding FDA CAPA findings Read More...
DE, USA
05/15/2011
21st International Congress of Clinical Chemistry and Laboratory Medicine  IFCC WorldLab 2011 - On behalf of the Congress Organizing Committee, it is a great pleasure to invite you to the joint IFCC WorldLab and EuroMedLab Berlin 2011 Congress. It is a great privilege for us to host this major joint event of Laboratory Medicine in the capital of Germany in May 2011. The 21st International Congress of Clinical Chemistry and Laboratory Medicine will take place together with the 19th European Congress of Clinical Chemistry and Laboratory Medicine as well as with the 8th Annual Meeting of the
21st International Congress of Clinical Chemistry and Laboratory Medicine IFCC WorldLab 2011
Course or Conference Sponsor : 21st International Congress of Clinical Chemistry and Laboratory Medicine
On behalf of the Congress Organizing Committee, it is a great pleasure to invite you to the joint IFCC WorldLab and EuroMedLab Berlin 2011 Congress. It is a great privilege fo Read More...
, Germany
05/13/2011
XII International Congress of Pediatric Laboratory Medicine - ICPLM - Come join us while we discuss this years top topics: Accessing health in children, 
National surveys and the role of the Laboratories 
Pediatric Obesity and Transition Care.


05/15/2011
XII International Congress of Pediatric Laboratory Medicine - ICPLM
Course or Conference Sponsor : International Congress of Pediatric Laboratory Medicine
Come join us while we discuss this years top topics: Accessing health in children, National surveys and the role of the Laboratories Pediatric Obesity and Transition Care. Read More...
, Germany
05/10/2011
Using Statistics to Determine Sample Size - Webinar By GlobalCompliancePanel - Overview: This webinar covers the statistical methods used to calculate sample sizes for both attribute and variables data.

Methods for collecting the sample will be covered.  Every sampling plan has risks. This webinar covers how to calculate Type I and Type II errors. A discussion of how the FDA views sampling plans, especially for validation and acceptance activities.  Sample size to ensure a certain level of process capability will be covered.

Areas Covered in the Session:

    * How
Using Statistics to Determine Sample Size - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panela
Overview: This webinar covers the statistical methods used to calculate sample sizes for both attribute and variables data. Methods for collecting the sample will be covere Read More...
DE, USA
05/10/2011
Using Statistics to Determine Sample Size - Webinar By GlobalCompliancePanel - Overview: This webinar covers the statistical methods used to calculate sample sizes for both attribute and variables data.

Methods for collecting the sample will be covered.  Every sampling plan has risks. This webinar covers how to calculate Type I and Type II errors. A discussion of how the FDA views sampling plans, especially for validation and acceptance activities.  Sample size to ensure a certain level of process capability will be covered.

Areas Covered in the Session:

    * How
Using Statistics to Determine Sample Size - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panel
Overview: This webinar covers the statistical methods used to calculate sample sizes for both attribute and variables data. Methods for collecting the sample will be covere Read More...
DE, USA
05/05/2011
Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs) - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panel
Overview: This webinar is designed to outline the characteristic of an effective work instruction, and Standard operating procedure. The webinar is also designed to help di Read More...
DE, USA
05/05/2011
Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs) - Webinar By GlobalCompliancePanel - Overview: This webinar is designed to outline the characteristic of an effective work instruction, and Standard operating procedure.

The webinar is also designed to help differentiate Work Instructions from Standard operating procedures. Attendees will learn the steps used to write effective work instructions and Standard operating procedures.

Why Should You Attend: The current shift in FDA thinking is that manufactures do not give their employees enough direction to perform their jobs. Th
Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs) - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panel
Overview: This webinar is designed to outline the characteristic of an effective work instruction, and Standard operating procedure. The webinar is also designed to help di Read More...
DE, USA
05/03/2011
FMEA and Risk Management for Medical Devices - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : global Compliance Panel
Overview: This presentation will explain the various terms used in risk management and the importance of ISO 14971 & ISO 13485 in the managements of risks during the life cycl Read More...
DE, USA
05/03/2011
FMEA and Risk Management for Medical Devices - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panel
Overview: This presentation will explain the various terms used in risk management and the importance of ISO 14971 & ISO 13485 in the managements of risks during the life cycl Read More...
DE, USA
04/22/2011
Process Validation for Medical Device Manufacturers
Course or Conference Sponsor : Compliance Online
This Process validation training/webinar for medical device manufacturers will discuss the CDRH interpretation of the GHTF guidance and how manufacturers should develop Proces Read More...
CA, USA
04/19/2011
Design History Files, Device Master Records, Device History Records, and Technical Files
Course or Conference Sponsor : Compliance Online
This webinar will examine the existing and proposed requirements for the FDA's DHF and the MDD's TF/DD. Their differing purposes / goals. Required and desirable contents. Area Read More...
CA, USA
04/13/2011
Off-Label Promotion of Medical Devices: Maximizing Your Performance Claims within FDA's Framework of Acceptable Practices - Webinar By GCPanel - Overview: The webinar covers
Off-Label Promotion of Medical Devices: Maximizing Your Performance Claims within FDA's Framework of Acceptable Practices - Webinar By GCPanel
Course or Conference Sponsor : Global Compliance Panel
Overview: The webinar covers "Off-label statute" and the FDA's nonbinding off-label guidance as relates to re-prints, performance claims, and Promotion. Emphasis is placed Read More...
DE, USA
04/13/2011
Off-Label Promotion of Medical Devices: Maximizing Your Performance Claims within FDA's Framework of Acceptable Practices - Webinar By GCPanel - Overview: The webinar covers
Off-Label Promotion of Medical Devices: Maximizing Your Performance Claims within FDA's Framework of Acceptable Practices - Webinar By GCPanel
Course or Conference Sponsor : Global Compliance Panel
Overview: The webinar covers "Off-label statute" and the FDA's nonbinding off-label guidance as relates to re-prints, performance claims, and Promotion. Emphasis is placed Read More...
DE, USA
04/08/2011
FDA's 2011 Revised 510(k) Premarket Notification Process - This 510(K) training will help you understand and be prepared for substantial changes to the Premarket Notification 510(k) process for Class II medical devices.

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.
FDA's 2011 Revised 510(k) Premarket Notification Process
Course or Conference Sponsor : Compliance Online
This 510(K) training will help you understand and be prepared for substantial changes to the Premarket Notification 510(k) process for Class II medical devices. NOTE: Use T Read More...
CA, USA
04/07/2011
Basics of testing associated with sterilization validation and routine processing
Course or Conference Sponsor : Compliance Online
This sterilization validation process training webinar will review the FDA or ISO requirements for tests following validation and emphasis is placed on the appropriate tests f Read More...
CA, USA
04/07/2011
Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries - Webinar By GlobalCompliancePanel - Overview: ISO 13485:2003 is a quality management system standard specially written for the medical device industry and is on the U S Food & Drug Administration (FDA) list of recognized consensus standards.

Medical device firms certified to ISO 13485:2003 will find themselves very closely compliant with FDA's Quality System Requirements under 21CFR 820. This presentation will help you to understand ISO 13485 and implement a successful quality management system, comparing it to ISO 9001 and FDA
Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panel
Overview: ISO 13485:2003 is a quality management system standard specially written for the medical device industry and is on the U S Food & Drug Administration (FDA) list of r Read More...
DE, USA
04/07/2011
Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panel
Overview: ISO 13485:2003 is a quality management system standard specially written for the medical device industry and is on the U S Food & Drug Administration (FDA) list of r Read More...
DE, USA
04/07/2011
HIPAA Business Associates: How the regulations have changed, and what you need to do for compliance now - Webinar By GCPanel - Overview: HIPAA Business Associate rules have changed in fundamental ways, with new responsibilities and obligations for HIPAA BAs.

The session will provide attendees the following tools, benefits, and solutions:

    * The audience will learn how business associates are now handled under the law and the proposed regulations and what has changed from the old rules.
    * The suggested and required content for a compliant business associate agreement will be presented.
    * Issues of how
HIPAA Business Associates: How the regulations have changed, and what you need to do for compliance now - Webinar By GCPanel
Course or Conference Sponsor : Global Compliance Panel
Overview: HIPAA Business Associate rules have changed in fundamental ways, with new responsibilities and obligations for HIPAA BAs. The session will provide attendees the f Read More...
DE, USA
04/07/2011
Dietary Supplements and Nutraceuticals: Compliance with FDA's Current Manufacturing Requirements - This webinar will describe the US GMP requirements and techniques to be compliant using easier, shorter and convenient strategies. We will discuss ways to demonstrate compliance to the current regulations and regulatory trends for the near future. Common findings and possible solutions will be discussed. Case studies will be presented for audit experiences in many countries including US, China, Israel, Taiwan, and India.

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.
Dietary Supplements and Nutraceuticals: Compliance with FDA's Current Manufacturing Requirements
Course or Conference Sponsor : Compliance Online
This webinar will describe the US GMP requirements and techniques to be compliant using easier, shorter and convenient strategies. We will discuss ways to demonstrate complian Read More...
CA, USA
04/07/2011
19th Annual Anti-Aging Medicine and Biomedical Technologies - Next spring, the world's leading anti-aging experts will gather in Orlando to convene the largest and most influential conference and expo worldwide on preventative medicine and bio-medical technologies!
19th Annual Anti-Aging Medicine and Biomedical Technologies
Course or Conference Sponsor :
Next spring, the world's leading anti-aging experts will gather in Orlando to convene the largest and most influential conference and expo worldwide on preventative medicine a Read More...
FL, USA
04/05/2011
Recent Major Industry CGMP Failures - Lessons Learned
Course or Conference Sponsor : Compliance Online
This cGMP webinar for medical device companies will focus on recent manufacturing lapses that have resulted in major recalls, multi-million dollar fines and some criminal char Read More...
CA, USA
04/05/2011
Verification vs. Validation in Regulated Industries
Course or Conference Sponsor : Compliance Online
Attend this webinar to understand the differences and benefits of verification and validation. Learn about the risks and complications involved with the application of sound v Read More...
CA, USA
03/31/2011
Build solid knowledge of GCP by learning the rules exactly as they appear in the official text - Get a complete understanding of GCP through a comprehensive analysis of GCP official text - NOTE FOR GUIDANCE ON GOOD CLINICAL PRACTICE, CPMP/ICH/135/95, July 2002.

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.
Build solid knowledge of GCP by learning the rules exactly as they appear in the official text
Course or Conference Sponsor : Compliance Online
Get a complete understanding of GCP through a comprehensive analysis of GCP official text - NOTE FOR GUIDANCE ON GOOD CLINICAL PRACTICE, CPMP/ICH/135/95, July 2002. NOTE: U Read More...
CA, USA
03/31/2011
Safety Reporting in Clinical Trials: Are you Ready for the New FDA Rules? - If your company or organization is involved in clinical trials, if you are a clinical site or safety monitoring/pharmacovigilance organization, if you with an IRB overseeing clinical trials, or if you are not sure of your compliance status with the current regulations, you can get valuable tips and training in less than an hour.

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.
Safety Reporting in Clinical Trials: Are you Ready for the New FDA Rules?
Course or Conference Sponsor : Compliance Online
If your company or organization is involved in clinical trials, if you are a clinical site or safety monitoring/pharmacovigilance organization, if you with an IRB overseeing c Read More...
CA, USA
03/30/2011
BioEnergy World Africa 2011 - Bio-Energy World Africa 2011 co-located with Africa's biggest energy show Power & Electricity World Africa provides the ideal platform for innovation, best practices and solutions to be sought.



http://www.terrapinn.com/2011/bioenergyza/img/header.gif?100903
BioEnergy World Africa 2011
Course or Conference Sponsor :
Bio-Energy World Africa 2011 co-located with Africa's biggest energy show Power & Electricity World Africa provides the ideal platform for innovation, best practices and solut Read More...
, South Africa
03/29/2011
Preparing for FDA GCP Inspections - Essentials for Sponsors and Clinical Sites - In this webinar, our speaker, a former FDA investigator, shares insight on how FDA prepares for an inspection, and reviews GCP regulations and FDA guidelines used for inspections. The presentation provides attendees from sponsor companies (pharmaceutical, biotech, device/diagnostics) and clinical sites with practical information on how to utilize quality improvement methods to effectively prepare for FDA GCP inspections.

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.
Preparing for FDA GCP Inspections - Essentials for Sponsors and Clinical Sites
Course or Conference Sponsor : Compliance online
In this webinar, our speaker, a former FDA investigator, shares insight on how FDA prepares for an inspection, and reviews GCP regulations and FDA guidelines used for inspecti Read More...
CA, USA
03/27/2011
SBS 17th Annual Conference & Exhibition - During this five-day event more than 2,000 scientists, innovators, researchers and industry analysts from around the globe will gather in Orlando to learn about the latest trends and basic and applied research that are transforming the way new pharmaceuticals are developed.

Exhibitors: The SBS 2011 Annual Conference & Exhibition is your opportunity to meet face-to-face with key leaders in the drug discovery community. Plan now to add this meeting to your 2011 calendar.
SBS 17th Annual Conference & Exhibition
Course or Conference Sponsor :
During this five-day event more than 2,000 scientists, innovators, researchers and industry analysts from around the globe will gather in Orlando to learn about the latest tre Read More...
FL, USA
03/27/2011
SBS 17th Annual Conference & Exhibition - During this five-day event more than 2,000 scientists, innovators, researchers and industry analysts from around the globe will gather in Orlando to learn about the latest trends and basic and applied research that are transforming the way new pharmaceuticals are developed.

Exhibitors: The SBS 2011 Annual Conference & Exhibition is your opportunity to meet face-to-face with key leaders in the drug discovery community. Plan now to add this meeting to your 2011 calendar.
SBS 17th Annual Conference & Exhibition
Course or Conference Sponsor :
During this five-day event more than 2,000 scientists, innovators, researchers and industry analysts from around the globe will gather in Orlando to learn about the latest tre Read More...
FL, USA
03/22/2011
An Introduction to FDA's Regulation of Human Cells, Tissues, and Cellular and Tissue-Based Products - This webinar will review FDA's regulatory oversight of stem cells-based products when used in humans and analyze its potential impact on the industry in the future. Learn FDA's criteria for marketing and promotion of stem cell-based products for therapeutic application.

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.
An Introduction to FDA's Regulation of Human Cells, Tissues, and Cellular and Tissue-Based Products
Course or Conference Sponsor : Compliance Online
This webinar will review FDA's regulatory oversight of stem cells-based products when used in humans and analyze its potential impact on the industry in the future. Learn FDA' Read More...
CA, USA
03/17/2011
Medical Device Complaints, MDR's and Recalls
Course or Conference Sponsor : Compliance Online
FDA warning letters and recalls are posted on FDA's website and published in trade magazines, newspapers available to firm's competitors, and has even driven the firm's stocks Read More...
CA, USA
03/16/2011
Identifying and managing unplanned protocol excursions and adhering to GCP
Course or Conference Sponsor : Compliance Online
This presentation will help participants identify key risk elements of protocol non-compliance, understand the responsibilities of the clinical research site and use effective Read More...
CA, USA
03/15/2011 to 03/16/2011
Compliance Asian Chemical Regulation-A two days free webinar
Course or Conference Sponsor : REACH 24h Consulting Group
As China, Japan and Korea recently updated their chemical management regulations, industries which focus on the Asian chemicals market may be impacted by the new compliance re Read More...
N/A, N/A
03/15/2011
Bringing Compliance To Design Control For Older Products - Webinar By GlobalCompliancePanel - Overview: The webinar examines critical parts of design control after product release including: design change control, design validation, and the Design History File.

The webinar is designed to help regulatory Affairs, Quality Engineers, and Design Engineers maintain released products within current regulatory requirements. As an attendee you will learn what the FDAs expectations for your released products are. You will also learn about the paper trail you are required to maintain to show co
Bringing Compliance To Design Control For Older Products - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance panel
Overview: The webinar examines critical parts of design control after product release including: design change control, design validation, and the Design History File. The Read More...
DE, USA
03/13/2011
Pittcon Conference  - Be part of the MUST ATTEND event for laboratory scientists. A recent survey found that over 80% of Pittcon attendees are decision makers.
Pittcon is the leading showcase for scientific and technical innovation. Thousands of conferees from more than 85 countries visit Pittcon each year to evaluate new products and technologies, formulate purchase decisions, and form valuable business connections. There is no better place to pursue laboratory business opportunities.
Pittcon Conference
Course or Conference Sponsor :
Be part of the MUST ATTEND event for laboratory scientists. A recent survey found that over 80% of Pittcon attendees are decision makers. Pittcon is the leading showcase for Read More...
GA, USA
03/10/2011
 Introduction to CE marking - In the EU it is the responsibility of the manufacturer to CE mark devices before placing them on the market.  The CE marking process consists of various steps including: Verifying the Essential requirements, product classification, choosing a conformity assessment route, testing , compiling a technical file, implementation and maintenance of a quality system, risk assessment, Implementation of a vigilance and Post Market Surveillance(PMS) system and appointing a European Authorized Representativ
Introduction to CE marking
Course or Conference Sponsor : Michor Consulting e.U.
In the EU it is the responsibility of the manufacturer to CE mark devices before placing them on the market. The CE marking process consists of various steps including: Verif Read More...
Webinar, Webinar
03/10/2011
Webinar On Differences between ICH-GCP and FDA regulations - The biopharmaceutical industry is also targeted by globalization. Biopharmaceuticals companies are running clinical trials all over the world and in order to lower the costs data is transferred between countries. In order to reduce time, to lower costs and to avoid delays in submission and market approval clinical professionals need to know the similarities and differences between the FDA and ICH-GCP requirements. 

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.
Webinar On Differences between ICH-GCP and FDA regulations
Course or Conference Sponsor : Compliance Online
The biopharmaceutical industry is also targeted by globalization. Biopharmaceuticals companies are running clinical trials all over the world and in order to lower the costs d Read More...
CA, USA
03/10/2011
How to Write SOPs: Tips on Writing the Perfect Document to Impress the FDA - Attend this webinar to learn what exactly an SOP should contain, what should be its format and tone, who should write it, when and how should it be revised or retired, how many SOPs should be there, what activities do not need SOPs, how should SOP training be conducted and documented, and many other issues impacting the compliance with FDA requirements from SOPs.

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.
How to Write SOPs: Tips on Writing the Perfect Document to Impress the FDA
Course or Conference Sponsor : Compliance Online
Attend this webinar to learn what exactly an SOP should contain, what should be its format and tone, who should write it, when and how should it be revised or retired, how man Read More...
CA, USA
03/10/2011
FDA's Proposed Rule Regarding Device Establishment Registration and Listing
Course or Conference Sponsor : Compliance Online
This Webinar will provide latest update as well as a "refresh" overview on how to register your device company and list your device(s) correctly and meeting requirements and e Read More...
CA, USA
03/08/2011
Design Control Explained - This course will cover the essential areas of the Design Control and the methods to effectively improve / implement them within the existing or new product development process. The training will also cover the proven methods for effectively driving the entire process.

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.
Design Control Explained
Course or Conference Sponsor : Compliance Online
This course will cover the essential areas of the Design Control and the methods to effectively improve / implement them within the existing or new product development process Read More...
CA, USA
03/05/2011
21st Annual Partnerships in Clinical Trials
Course or Conference Sponsor : Institute for Internatinal Research
As THE meeting place where you can find all of your partners under one roof, Partnerships is known for strategic program content that drives business forward and for unparalle Read More...
FL, USA
03/04/2011
Clinical Trial auditing - Identifying risks and building a more compliant and successful trial - This webinar will help with preparing the site and the study team with how to successfully prepare for an audit, how to identify risk of noncompliance, what to do before, during and after an audit. The session will give you practical solutions to get the best results from an audit and the opportunity to grow the image of your team and/or your site. 

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.
Clinical Trial auditing - Identifying risks and building a more compliant and successful trial
Course or Conference Sponsor : Compliance Online
This webinar will help with preparing the site and the study team with how to successfully prepare for an audit, how to identify risk of noncompliance, what to do before, duri Read More...
CA, USA
02/08/2011
Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - Webinar By GlobalCompliancePanel - Overview: In this Clinical Trial Audits training learn the risk management and best practices of GCP audit by reviewing and analyzing recent GCP audit finding from Clinical Investigators (Sites), Sponsors, and Institutional Review Boards (IRBs).

Why you should attend: Quality assurance is defined as a
Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : global Compliance Panel
Overview: In this Clinical Trial Audits training learn the risk management and best practices of GCP audit by reviewing and analyzing recent GCP audit finding from Clinical In Read More...
DE, USA
01-27-2011
European Union Medical Device Legislation Update - In the EU rules relating to the safety and performance of medical devices were harmonized in the 1990s.  The legal framework consists of 3 main directives: Directive 90/385/EEC regarding active implantable medical devices, Directive 93/42/EEC regarding medical devices and Directive 98/79/EC regarding in vitro diagnostic medical devices.  These 3 main directives have been supplemented over time by several modifying and implementing directives, including the last technical revision brought about b
European Union Medical Device Legislation Update
Course or Conference Sponsor : Michor Consulting e.U.
In the EU rules relating to the safety and performance of medical devices were harmonized in the 1990s. The legal framework consists of 3 main directives: Directive 90/385/EE Read More...
N/A, N/A
01/26/2011
15th Annual Drug Delivery Partnerships - Drug Delivery Partnerships is the pharmaceutical industry event where deals are made. Over 400 Business Development executives from Pharma, Biotech, Specialty Pharma, Generics and Drug Delivery companies convene every year to discuss the latest innovations in drug delivery and the most important mergers, acquisitions and partnerships impacting the life science industry. As the largest global pharmaceutical conference for business development executives, attending DDP provides participants unique
15th Annual Drug Delivery Partnerships
Course or Conference Sponsor : Institute for International Research (IIR),
Drug Delivery Partnerships is the pharmaceutical industry event where deals are made. Over 400 Business Development executives from Pharma, Biotech, Specialty Pharma, Generics Read More...
FL, US
01/20/2011
RSC Antibiotics 2011 - Where Now?  - This timely, focused meeting builds upon the highly successful event in 2008 attended by over 170 delegates. It brings together international experts from big pharma, spin-out start ups, academics and national reference laboratories to provide an over-arching view of the field.

http://www.rsc.org/images/061057---Antibiotics-flyer-_tcm18-186430.jpg
RSC Antibiotics 2011 - Where Now?
Course or Conference Sponsor : Royal Society of Chemistry
This timely, focused meeting builds upon the highly successful event in 2008 attended by over 170 delegates. It brings together international experts from big pharma, spin-out Read More...
London, UK
01/18/2011
How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant? - Webinar By GlobalCompliancePanel - This Webinar deals with what happens, and under what circumstances, when the protocol is not followed (PNF) and why this is of particular significance.

Covered, will be how a protocol deviation with the least significant effect where there is no substantive effect on the risks to research participants, no substantial effect of the value or integrity of the data, and did not result from willful or knowing misconduct on the part of the investigator is handled.

It will be important to see wha
How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant? - Webinar By GlobalCompliancePanel
Course or Conference Sponsor : Global Compliance Panel
This Webinar deals with what happens, and under what circumstances, when the protocol is not followed (PNF) and why this is of particular significance. Covered, will be how Read More...
DE, USA
01/15/2011
 NAVC Conference - 1. The first veterinary conference of the calendar year. Ideal for product launches, company announcements, new promotions
2. Large and most exciting national veterinary conference with over 15,000 veterinary professionals attending
3. Support staff that is second to none in meeting your needs and making you welcome
4. Two large exhibit halls visited by 98% of attendees
5. The Florida sunshine - in January, need we say more?
NAVC Conference
Course or Conference Sponsor :
1. The first veterinary conference of the calendar year. Ideal for product launches, company announcements, new promotions 2. Large and most exciting national veterinary conf Read More...
FL, USA

 

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