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Regulatory Courses and Conferences

Regulatory Education & Training Provider SPONSOR
Science and laboratory conferences, conventions, seminars, training courses and annual meetings in microbiology, toxicology, preclinical, food science, analytical chemistry, pharmaceuticals, bioanalytical, genetics, immunology, etc.
Advance your career with regulatory affairs, quality assurance, quality control, pharmaceuticals, medical devices, biotechnology, food, cosmetics, and clinical trials training courses, webinars, seminars, conferences, and on-line courses! Need to attend specific training not listed or need to have training in-house for your company? Submit Regulatory Training Request.
2006 Regulatory Courses and Conferences
start date
sponsor
training regulatory courses and conferences description.
12/23/2006
Generics Asia 2006
Generics Asia 2006
Sponsor: IBC Asia (S) Pte Ltd
12/04/2006
7th European Electronic Document Management Conference
7th European Electronic Document Management Conference
Sponsor: Drug Information Association (DIA)
12/04/2006
1st Annual Cardiac Safety Conference
1st Annual Cardiac Safety Conference
Sponsor: Drug Information Association (DIA)
11/29/2006
Critical Process Cleaning and Cleaning Validation
Critical Process Cleaning and Cleaning Validation
Sponsor: The Center for Professional Advancement (CfPA)
11/29/2006
Cleaning Validation and Best Practices for Cleaning Processes
Cleaning Validation and Best Practices for Cleaning Processes
Sponsor: Institute of Validation Technology (IVT)
11/27/2006
Best Practices and Development of Standards for the Submission of Genomic Data to the FDA
Best Practices and Development of Standards for the Submission of Genomic Data to the FDA
Sponsor: Drug Information Association (DIA)
11/27/2006
C5 International's European Freedom to Operate Congress
C5 International's European Freedom to Operate Congress
Sponsor: C5 International
11/27/2006
Auditing and Inspecting Preclinical Research for GLP Compliance
Auditing and Inspecting Preclinical Research for GLP Compliance
Sponsor: The Center for Professional Advancement (CfPA)
11/27/2006
Auditing and Inspecting Preclinical Research for GLP Compliance
Auditing and Inspecting Preclinical Research for GLP Compliance
Sponsor: The Center for Professional Advancement (CfPA)
11/27/2006
Pharmacovigilance Training: Clinical Trials and Marketed Products
Pharmacovigilance Training: Clinical Trials and Marketed Products
Sponsor: Drug Information Association (DIA)
11/27/2006
European Regulatory Affairs
Sponsor: Drug Information Association (DIA)
11/20/2006
Process Validation for Packaging of Pharmaceuticals & Medical Devices
Process Validation for Packaging of Pharmaceuticals & Medical Devices
Sponsor: The Center for Professional Advancement (CfPA)
11/15/2006
Packaging of Pharmaceuticals
Packaging of Pharmaceuticals
Sponsor: Center for Professional Advancement (CfPA)
11/14/2006
DIA 7th Middle East Regulatory Conference (MERC)
DIA 7th Middle East Regulatory Conference (MERC)
Sponsor: Drug Information Association (DIA)
11/13/2006
Investigational Supply Process Training Course
Investigational Supply Process Training Course
Sponsor: Drug Information Association (DIA)
11/13/2006
European Regulatory Affairs
European Regulatory Affairs
Sponsor: Drug Information Association (DIA)
11/13/2006
Overview of Drug Development
Overview of Drug Development
Sponsor: Drug Information Association (DIA)
11/13/2006
Regulatory II: The CTD/NDA Phase
Regulatory II: The CTD/NDA Phase
Sponsor: Drug Information Association (DIA)
11/13/2006
Pharmaceutical cGMPs and FDA Inspections
Sponsor:
11/07/2006
Cell Based Assays in Drug Development for Biopharmaceuticals
Cell Based Assays in Drug Development for Biopharmaceuticals
Sponsor: Institute for International Research USA (IIR USA)
11/06/2006
Process Analytical Technology
Process Analytical Technology
Sponsor: Center for Professional Advancement (CfPA)
10/30/2006
Drug Development In China
Drug Development In China
Sponsor: Cambridge Health Institute
10/29/2006
DIA's 4th Canadian Annual Meeting what will the regulatory landscape look like in the next decade? Challenges for regulatory and industry
DIA's 4th Canadian Annual Meeting what will the regulatory landscape look like in the next decade? Challenges for regulatory and industry
Sponsor: Drug Information Association (DIA)
10/24/2006
Institute for Validation Technology's 12th Annual Validation Week
Institute for Validation Technology's 12th Annual Validation Week
Sponsor: Institute of Validation Technology (IVT)
10/23/2006
Special Training Course on US Regulatory Affairs
Special Training Course on US Regulatory Affairs
Sponsor: Drug Information Association (DIA)
10/17/2006
Method Validation
Method Validation
Sponsor: Institute of Validation Technology
10/17/2006
Method Validation
Method Validation
Sponsor: Institute of Validation Technology
10/16/2006
Drug Discovery and Development in India
Drug Discovery and Development in India
Sponsor: Drug Information Association (DIA)
10/16/2006
Fundamentals of Clinical Research Monitoring
Fundamentals of Clinical Research Monitoring
Sponsor: Drug Information Association (DIA)
10/16/2006
First International DIA Workshop: Developing Probiotics as Foods and Drugs - Scientific and Regulatory Challenges
First International DIA Workshop: Developing Probiotics as Foods and Drugs - Scientific and Regulatory Challenges
Sponsor: Drug Information Association (DIA)
10/16/2006
Clinical Data Management
Clinical Data Management
Sponsor: Drug Information Association (DIA)
10/12/2006
Medical Imaging Conference Critical Path Opportunities List: From Opportunities to Action
Medical Imaging Conference Critical Path Opportunities List: From Opportunities to Action
Sponsor: Drug Information Association (DIA)
10/10/2006
Special Seminar on European Regulatory Affairs
Special Seminar on European Regulatory Affairs
Sponsor: Drug Information Association (DIA)
10/05/2006
Drug Information Associations's 3rd Multitrack meeting in Japan
Drug Information Associations's 3rd Multitrack meeting in Japan
Sponsor: Drug Information Association (DIA)
10/05/2006
Overview for Regulatory Affairs Personnel on the Requirements for Submission of Clinical Data for NDAs
Overview for Regulatory Affairs Personnel on the Requirements for Submission of Clinical Data for NDAs
Sponsor: Drug Information Association (DIA)
10/04/2006
Practical GCP Compliance Auditing of Trials & Systems
Practical GCP Compliance Auditing of Trials & Systems
Sponsor: Drug Information Association (DIA)
10/04/2006
Statistical Methodology in Clinical R&D
Statistical Methodology in Clinical R&D
Sponsor: Drug Information Association (DIA)
10/03/2006
EudraVigilance: Medicinal Product Dictionary
EudraVigilance: Medicinal Product Dictionary
Sponsor: Drug Information Association (DIA)
10/03/2006
Institute for Validation Technology's Validation and Compliance Summit
Institute for Validation Technology's Validation and Compliance Summit
Sponsor: Institute of Validation Technology (IVT)
10/03/2006
Institute for Validation Technology's  Validation and Compliance Summit
Institute for Validation Technology's Validation and Compliance Summit
Sponsor: Institute of Validation Technology (IVT)
09/28/2006
Celebrating the Two-Year Milestone and Planning for the Future of Voluntary Genomic Data Submissions (VGDS) to the FDA
Celebrating the Two-Year Milestone and Planning for the Future of Voluntary Genomic Data Submissions (VGDS) to the FDA
Sponsor: Drug Information Association (DIA)
09/26/2006
Investigating Out-of-Specification Results
Investigating Out-of-Specification Results
Sponsor: Institute of Validation Technology (IVT)
09/26/2006
Investigating Out-of-Specification Results
Investigating Out-of-Specification Results
Sponsor: Institute of Validation Technology
09/26/2006
Optimizing Cell Culture Development
Optimizing Cell Culture Development
Sponsor: Cambridge Health Institute
09/26/2006
Global Electronic Labeling
Global Electronic Labeling
Sponsor: Drug Information Association (DIA)
09/25/2006
Introduction to Good Clinical Practices and Auditing
Introduction to Good Clinical Practices and Auditing
Sponsor: Drug Information Association (DIA)
09/25/2006
Bridging the Gaps between GCP, Clinical Trial Safety and Postmarketing Vigilance: Regulatory Compliance Challenges for International Pharmaceutical and Medical Device Companies
Bridging the Gaps between GCP, Clinical Trial Safety and Postmarketing Vigilance: Regulatory Compliance Challenges for International Pharmaceutical and Medical Device Companies
Sponsor: Drug Information Association (DIA)
09/25/2006
3rd Latin American Congress for Clinical Research: Advanced Topics in Clinical Research/Drug Development for Clinical Research Professionals
3rd Latin American Congress for Clinical Research: Advanced Topics in Clinical Research/Drug Development for Clinical Research Professionals
Sponsor: Drug Information Association (DIA)
09/18/2006
Clinical Research and Drug Registration in China and India
Clinical Research and Drug Registration in China and India
Sponsor: Drug Information Association (DIA)
09/18/2006
European Union (EU) Pharmaceutical Law & Regulation
European Union (EU) Pharmaceutical Law & Regulation
Sponsor: C5 International
09/18/2006
Drug Safety Surveillance and Epidemiology
Drug Safety Surveillance and Epidemiology
Sponsor: Drug Information Association (DIA)
09/18/2006
Regulatory I: The Investigational New Drug IND  Phase
Regulatory I: The Investigational New Drug IND Phase
Sponsor: Drug Information Association (DIA)
09/15/2006
Developing Standard Operating Procedures
Developing Standard Operating Procedures
Sponsor: Drug Information Association (DIA)
09/11/2006
Non-Clinical Drug Safety Evaluation and Drug Development
Non-Clinical Drug Safety Evaluation and Drug Development
Sponsor: The Center for Professional Advancement (CFPA)
09/04/2006
European Regulatory Affairs
European Regulatory Affairs
Sponsor: Drug Information Association (DIA)
08/28/2006
Regulatory II: The CTD/NDA Phase
Regulatory II: The CTD/NDA Phase
Sponsor: Drug Information Association (DIA)
08/28/2006
European Regulatory Affairs
European Regulatory Affairs
Sponsor: Drug Information Association (DIA)
08/22/2006
EudraVigilance: Medicinal Product Dictionary
EudraVigilance: Medicinal Product Dictionary
Sponsor: Drug Information Associaiton (DIA)
08/22/2006
Cancer Immunotherapeutics & Vaccines
Cancer Immunotherapeutics & Vaccines
Sponsor: Cambridge Health Institute
08/22/2006
RFID Technology within Healthcare and Pharmaceuticals
RFID Technology within Healthcare and Pharmaceuticals
Sponsor: Institute of Validation Technology (IVT)
08/21/2006
Targeted Cancer Therapies
Targeted Cancer Therapies
Sponsor: Cambridge Health Institute (CHI)
08/15/2006
IVT's Medical Device Design, Manufacturing, Validation, Compliance Conference
IVT's Medical Device Design, Manufacturing, Validation, Compliance Conference
Sponsor: IVT - Institute of Validation Technology
08/15/2006
Laboratory Regulations, Controls and Compliance
Laboratory Regulations, Controls and Compliance
Sponsor: Institute of Validation Technology (IVT)
08/07/2006
Overview of Drug Development
Overview of Drug Development
Sponsor: Drug Information Association (DIA)
08/07/2006
Fundamentals of Clinical Research Monitoring
Fundamentals of Clinical Research Monitoring
Sponsor: Drug Information Association (DIA)
08/07/2006
Regulatory Affairs: Part I: The IND Phase & Part II: The CTD/NDA Phase
Regulatory Affairs: Part I: The IND Phase & Part II: The CTD/NDA Phase
Sponsor: Drug Information Association (DIA)
07/31/2006
Senior RA Institute II: Post-Launch Challenges of Growth
Senior RA Institute II: Post-Launch Challenges of Growth
Sponsor: Regulatory Affairs Professionals Society (RAPS)
07/27/2006
2nd Annual Obesity Drug Development Summit
2nd Annual Obesity Drug Development Summit
Sponsor: The Center for Business Intelligence
07/24/2006
Pediatric Clinical Research: Where Are We and Where Do We Go From Here?
Pediatric Clinical Research: Where Are We and Where Do We Go From Here?
Sponsor: Drug Information Association (DIA)
07/10/2006
Good Laboratory Practices (GLP)
Good Laboratory Practices (GLP)
Sponsor: PERI-The Pharmaceutical Education and Research Institute, Inc.
07/10/2006
Development Strategies and Clinical Trial Methods for Oncologic Products
Development Strategies and Clinical Trial Methods for Oncologic Products
Sponsor:
06/26/2006
Aseptic Processing and Sterile Processes
Aseptic Processing and Sterile Processes
Sponsor: The Institute of Validation Technology (IVT)
06/20/2006
Risk Assessment and Management
Risk Assessment and Management
Sponsor: The Institute for Validation Technology (IVT)
06/19/2006
Cleaning Validation & Best Practices for Cleaning Processes
Cleaning Validation & Best Practices for Cleaning Processes
Sponsor: Institute of Validation Technology (IVT)
06/13/2006
Process Analytical Technology
Process Analytical Technology
Sponsor: The Institute of Validation Technology
06/12/2006
PERI's Global Regulatory Affairs: Overview of Drugs and Biologics
PERI's Global Regulatory Affairs: Overview of Drugs and Biologics
Sponsor: PERI-The Pharmaceutical Education and Research Institute, Inc.
06/01/2006
European Conference: EU Regulatory Response to Innovation and Global Competitiveness
European Conference: EU Regulatory Response to Innovation and Global Competitiveness
Sponsor: Regulatory Affairs Professionals Society (RAPS)
06/01/2006
European Regulatory Affairs
European Regulatory Affairs
Sponsor: Drug Information Association (DIA)
06//20/2006
Microbiology Event of the Year
Microbiology Event of the Year
Sponsor: Institute of Validation Technology (IVT)
05-22-2006
Institute for International Research's 7th Annual  Immunogenicity Studies for Biotherapeutics
Institute for International Research's 7th Annual Immunogenicity Studies for Biotherapeutics
Sponsor: Institute for International Research (IIR)
05-15-2006
Institute for International Research's 6th Annual Impurities Conference
Institute for International Research's 6th Annual Impurities Conference
Sponsor: Institute for International Research (IIR)
05/22/2006
Development Standard Operating Procedures (SOPs)
Development Standard Operating Procedures (SOPs)
Sponsor: Drug Information Association (DIA)
05/22/2006
Joint DIA/HESI/SAPS Conference on Environmental Assessment of Human Medicines
Joint DIA/HESI/SAPS Conference on Environmental Assessment of Human Medicines
Sponsor: Drug Information Association (DIA)
05/16/2006
DIA Workshop on: New Vaccines Development
DIA Workshop on: New Vaccines Development
Sponsor: Drug Information Association (DIA)
05/16/2006
European Regulatory Chemistry Manufacturing & Control
European Regulatory Chemistry Manufacturing & Control
Sponsor: Drug Information Association (DIA)
05/08/2006
Regulatory I: The IND Phase
Regulatory I: The IND Phase
Sponsor: Drug Information Association (DIA)
05/03/2006
Clinical Trial Delays - Assuring Predictable and Timely Completion of Patient Enrollment
Clinical Trial Delays - Assuring Predictable and Timely Completion of Patient Enrollment
Sponsor: Drug Information Association (DIA)
05/01/2006
Overview of Drug Development.
Overview of Drug Development.
Sponsor: Drug Information Association (DIA)
05/01/2006
European Regulatory Affairs
European Regulatory Affairs
Sponsor: Drug Information Association ( DIA )
04/24/2006
Transportation of Biologicals and Biotechnology Products
Transportation of Biologicals and Biotechnology Products
Sponsor: International Quality and Productivity Center
04/18/2006
2006 FDA Science Forum - A Century of FDA Science: Pioneering the Future of Public Health
2006 FDA Science Forum - A Century of FDA Science: Pioneering the Future of Public Health
Sponsor: Drug Information Association (DIA)
04/13/2006
The Second Multitrack Workshop in Japan
The Second Multitrack Workshop in Japan
Sponsor: Drug Information Association (DIA)
04/03/2006
Electronic Transmission of Individual Case Safety  Reports in the US and EU
Electronic Transmission of Individual Case Safety Reports in the US and EU
Sponsor: Drug Information Association
04/03/2006
Fundamentals of Clinical Research Monitoring Training Course
Fundamentals of Clinical Research Monitoring Training Course
Sponsor: Drug Information Association
03/30/2006
Qualification of Laboratory Instruments
Qualification of Laboratory Instruments
Sponsor: PTi international
03/28/2006
Aseptic Processing and Sterile Processes
Aseptic Processing and Sterile Processes
Sponsor: Institute of Validation Technology
03/23/2006
Developments in Medical Device Testing
Developments in Medical Device Testing
Sponsor: NAMSA
03/08/ 2006
Gene Therapy Research - From the Bench to the Clinic to Commercialization
Gene Therapy Research - From the Bench to the Clinic to Commercialization
Sponsor: The Center for Business Intelligence
03/02/2006
2nd Annual Stem Cell Research & Therapeutics
2nd Annual Stem Cell Research & Therapeutics
Sponsor: GTC Bio
02/16/2006
Complying with FDA/ICH Requirements for Stability Testing
Complying with FDA/ICH Requirements for Stability Testing
Sponsor: PTi international
01/30/2006
Achieving and Maintaining Laboratory cGMP Compliance
Achieving and Maintaining Laboratory cGMP Compliance
Sponsor: PTi international
01/26/ 2006
Menopause Pharmacotherapeutic Development
Menopause Pharmacotherapeutic Development
Sponsor: The Center for Business Intelligence
01/20/2006
Safety Testing of Drug Metabolites: The Impact on Clinical and Toxicology Programs
Safety Testing of Drug Metabolites: The Impact on Clinical and Toxicology Programs
Sponsor: Barnett Educational Services
>
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2007 Laboratory Calendar

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International Regulatory News

FDA takes steps to protect public health Agency working with animal, drug and medical communities to promote judicious antimicrobial use
2012-04-11 00:00:00
The U.S. Food and Drug Administration announced today that it is taking three steps to protect public health and promote the judicious use of medically important antibiotics in food-producing animals. Antimicrobial resistance occurs when bacteria... 

Department of Justice enters consent decree with California seafood processor Company agrees to multiple actions to correct FDA food safety violations
2012-04-11 00:00:00
A California seafood importer and processor has agreed to a consent decree with the FDA that prevents the company from manufacturing or distributing fish or fish products until it has corrected conditions in its seafood processing facility alleged to... 

FDA announces plans to pilot end-stage kidney disease technology in new program
2012-04-10 00:00:00
Innovation Pathway aims to reduce time and cost of bringing safe and effective, breakthrough technologies to patients Three products for patients with end stage renal disease (ESRD) have been chosen to participate in the FDA's Innovation Pathway, ... 

Akron Rubber Development Laboratory, Inc's Time Domain (TD) Nuclear Magnetic Resonance (NMR) Capabilities Expand to Help Meet Today's Quality Assurance Needs
2012-04-09 00:00:00
Akron, OH - Determining the state of cure of elastomeric materials is becoming more and more important to today's material development companies and parts manufacturers. Quality Assurance Managers, Production Managers and Material Development Engine... 

Akron Rubber Development Laboratory, Inc Adds to Its Accreditation Independent High Pressure / High Temperature Aging, Rapid Gas Decompression (RGD) Testing and Service Life Prediction Capabilities for Materials Used in the Oil and Gas Industry
2012-04-09 00:00:00
Akron, OH - Polymer engineering and material qualification for oil and gas applications is a daily challenge for engineers as they deal with ever higher pressures and temperatures at new depths and in new gases. Akron Rubber Development Laboratory,... 

FDA enters consent decree with cheese producer due to Listeria contamination
2012-04-09 00:00:00
Washington state cheese processor agrees to FDA food safety action A Washington state cheese processor and distributor has agreed to keep its products off the market until they are proven safe for consumption as part of a consent decree of permane... 

CLSI Publishes Revised Guideline on Nucleic Acid Amplification Assays for Molecular Hematopathology
2012-04-05 00:00:00
The Clinical and Laboratory Standards Institute (CLSI) recently published Wayne, Pennsylvania, USA-April 2012-Clinical and Laboratory Standards Institute (CLSI) recently published Nucleic Acid Amplification Assays for Molecular Hematopathology; Appro... 

FDA proposes lower risk classification for certain tuberculosis tests
2012-04-04 00:00:00
Lower classification will support CDC recommendations The Food and Drug Administration issued a proposed rule today that would encourage the development of a type of test used to detect cases of tuberculosis (TB). This rule would lower the current... 

Avomeen Analytical Services Renews Registration with Contract Laboratory .com
2012-04-03 00:00:00
Contract Laboratory Inc. is pleased to announce that Avomeen Analytical Services has become a member of its Laboratory Outsource Network - ContractLaboratory.com. Avomeen Analytical Services is a full-service chemical testing laboratory specializi... 

ARDL's Time Domain (TD) Nuclear Magnetic Resonance (NMR) Capabilities Expand to Help Meet Today's Quality Assurance Needs
2012-04-02 00:00:00
For Immediate Release: April 2, 2012 From: 2887 Gilchrist Road Akron, OH 44305 p.330.794.6600 f.330.794.6610 www.ardl.com ARDL's Time Domain (TD) Nuclear Magnetic Resonance (NMR) Capabilities Expand to Help Meet Today's Quality A... 

Ramboll Finland Registers with Contract Laboratory .com
2012-04-02 00:00:00
Contract Laboratory Inc. is pleased to announce that Ramboll Finland has become a member of its Laboratory Outsource Network - ContractLaboratory.com. Ramboll is a truly multi-disciplinary engineering, design and consultancy company working to mee... 

New FDA guidance on considerations used in device approval, de novo decisions
2012-04-01 00:00:00
Clinical data, risks, benefits and patient risk tolerance outlined in process The U.S. Food and Drug Administration today published a first-of-a-kind guidance1 for medical device manufacturers, describing how the benefits and risks of certain medi... 

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Would your company like to sponsor or advertise in the Contract Laboratory .com Laboratory Events Calendar? Advertising, sponsorship or media partnerships are available. Please contact us 403-770-1992 at email us
News
FDA takes steps to protect public health Agency working with animal, drug and medical communities to promote judicious antimicrobial use
2012-04-11 00:00:00
The U.S. Food and Drug Administration announced today that it is taking thr... 

Department of Justice enters consent decree with California seafood processor Company agrees to multiple actions to correct FDA food safety violations
2012-04-11 00:00:00
A California seafood importer and processor has agreed to a consent decree ... 

FDA announces plans to pilot end-stage kidney disease technology in new program
2012-04-10 00:00:00
Innovation Pathway aims to reduce time and cost of bringing safe and effect... 

FDA enters consent decree with cheese producer due to Listeria contamination
2012-04-09 00:00:00
Washington state cheese processor agrees to FDA food safety action A Was... 

FDA proposes lower risk classification for certain tuberculosis tests
2012-04-04 00:00:00
Lower classification will support CDC recommendations The Food and Drug ... 

New FDA guidance on considerations used in device approval, de novo decisions
2012-04-01 00:00:00
Clinical data, risks, benefits and patient risk tolerance outlined in proce... 

Obama administration takes action to address tobacco epidemic
2012-03-30 00:00:00
Today the U.S. Food and Drug Administration (FDA) released two separate dra... 

FDA approves additional blood test for viruses linked to leukemia, neurologic diseases
2012-03-27 00:00:00
Avioq HTLV-I/II Microelisa System, a test designed to detect antibodies to ... 

FDA proposes lower risk classification for certain tuberculosis tests Lower classification will support CDC recommendations
2012-03-25 00:00:00
The Food and Drug Administration issued a proposed rule today that would en... 

OSHA and the Society for Chemical Hazard Communication renew Alliance to promote best practices to reduce worker exposures to chemical hazards
2012-03-23 00:00:00
WASHINGTON - Promoting best practices to reduce worker exposure to hazardou... 

 

Global Regulatory .com values your privacy. For more information on our Privacy Policy, please visit Privacy Policy Please also visit Contract Laboratory.com,, Contract Clinical.com

This site is owned and managed by Global Regulatory, Inc.