Organiser

Global Compliance Panel

globalcompliancepanel.com

Events organised

Last: 2014
The DHF, Technical File and Design Dossier - Similarities, Differences and The Future
Las Vegas, Nevada
Last: 2014
Statistical Considerations for ICH Guidelines Seminar
Sydney, Australia
Last: 2014
How to Get Your Combination Product Approved and onto the US Marketplace Seminar
Last: 2014
Advertising and Promotional Requirements for Drugs and Medical Devices
San Diego, California
Last: 2014
Live Seminar: Advertising and Promotional Requirements for Drugs and Medical Devices
San Diego, California
Last: 2014
2day Inperson seminar on Combination Products How to Get Your Combination Product Approved
Last: 2014
2-day In-person Seminar Statistical Considerations for ICH Guidelines
Sydney, Australia
Last: 2014
2-day In-person Seminar FDA Based Guidelines on Statistical Sampling Plans
Singapore
Last: 2014
2day Inperson Seminar on FDAs and the US Customs Border Patrols Import
Culver City, California
Last: 2014
2-day In-person Seminar on "Applying ISO14971:2012 and IEC62304 - A Guide to Practical Risk Manageme
Last: 2014
How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare
Palm Beach, Florida
Last: 2014
The Most Common Problems with Software Validation Processes
Palm Beach, Florida
Last: 2014
Measurement Uncertainty in Microbiology
Palm Beach, Florida
Last: 2014
Key Concepts in Successful Water System Sanitization
Palm Beach, Florida
Last: 2014
ICH GCPs and the Clinical Research Process (Including Phase 0,1,2,3 and Phase 4 trials)
Palm Beach, Florida
Last: 2014
Excel Spreadsheet Validation for FDA 21 CFR Part 11
Palm Beach, Florida
Last: 2014
2-day In-person Seminar Global Medical Device Regulations - US, EU and Canada
Chicago, Illinois
Last: 2014
2-day In-person Seminar GMP Compliance for Pharmaceutical Quality Control Laboratories
Berlin, Germany
Last: 2014
Live In-Person Seminar on “GMP Compliance for Pharmaceutical Quality Control Laboratories”
Last: 2014
2-day In-person Seminar on Advanced Course: Validation & 21 CFR 11 Compliance
Washington, District of Columbia
Last: 2014
2-day In-person Seminar on Global Medical Device Regulation
Chicago, Illinois
Last: 2014
GMP Compliance for Pharmaceutical Quality Control Laboratories: 2-day In-person Seminar
Hong Kong
Last: 2014
2-day In-person Seminar on “Validate Your Own Excel Spreadsheet Application Workshop”
Last: 2014
2day In-person Seminar on “The A to Z's of HIPAA Privacy, Security, and Breach Notification Rules”
Raleigh, North Carolina
Last: 2014
2-day In-person Seminar on “Combination Products
San Francisco, California
Last: 2014
2-day In-person Seminar on “Applying ISO14971:2012 and IEC62304
Berlin, Germany
Last: 2014
2-day In-person Seminar on “Quality System Regulations for Drugs, Devices, and Tablets
Philadelphia, Pennsylvania
Last: 2014
Seminar on The DHF, Technical File and Design Dossier - Similarities, Differences and the Future
Las Vegas, Nevada
Last: 2014
2-day In-person Seminar on “Quality Audits for the Medical Device Industry”
Raleigh, North Carolina
Last: 2014
2-day In-person Seminar on “The A to Z's of HIPAA Privacy, Security, and Breach Notification Rules”
Raleigh, North Carolina
Last: 2014
2-day In-person Seminar on Validation and Part 11/Annex11
Singapore
Last: 2015
GMP Expectations for Products Used in Early Phase IND Studies
Palm Beach, Florida
Last: 2015
ATC Radar Approach Control (TRACON)
Palm Beach, Florida
Last: 2015
In-person Seminar on The A to Z's of Microbial Control, Monitoring, Validation &Troubleshooting
Dhaka, Bangladesh
Last: 2015
The A to Z's of Microbial Control, Monitoring, Validation and Troubleshooting
Dhaka, Bangladesh
Last: 2016
Lymphoma and Myeloma - International Congress on Hematologic Malignancies
Mumbai, India
Last: 2015
HIPAA Privacy Security - Time to Get Serious Conference - Chicago, IL
Chicago, Illinois
Last: 2015
Enterprise Risk Management In The New World Seminar
Chicago, Illinois
Last: 2015
Marketing Products without Getting Hammered by FDA at Zurich, Switzerland
NO CITY, Switzerland
Last: 2015
Singapore Conference on Good Manufacturing Practice Compliance for Pharmaceutical Quality
Singapore
Last: 2015
2-day In-person Seminar on Validation and Part 11 Compliance of Computer Systems and Data
Mumbai, India
Last: 2016
2-day In-person Seminar Air Traffic Control: How it REALLY works!
Last: 2016
A Matter of Ethics: Facing the Fear of Doing the Right Thing
Last: 2016
2-day In-person Seminar Conducting Internal Investigations
Last: 2016
2-day In-person Seminar Tax and Accounting Strategies for Residential Real Estate Investors
Last: 2016
2-day In-person Seminar FDA Device Software Regulation
San Diego, California
Last: 2016
2-day In-person Seminar The A to Z's of HIPAA Compliance
Last: 2016
Applying U.S. FDA Laws and Regulations to Each Phase of Total Product Life Cycle (TPLC) Seminar
San Diego, California
Last: 2016
2-day In-person Seminar Effective Audit Report Writing
Last: 2016
Food Safety & Defense: Key Factors to Safely Manufacture, Package & Handle Food Products
Kenner, Louisiana
Last: 2016
Internal Auditing for the Medical Device Industry Seminar
Last: 2016
2-day In-person Seminar Advanced Payroll
Last: 2016
Cash Management: A User's Perspective - The How's, Why's and Wherefores
Last: 2016
Seminar on Why is FDA at my Facility, and what do I do During an Inspection
Last: 2016
Seminar on Mastering Biofilm Control, Monitoring, Validation and Excursion Investigations
Last: 2016
Cape Town Seminar on How to Prepare For and Survive During an FDA Inspection
Last: 2016
Cape Town Seminar on Complaint Handling and Management
Last: 2017
GMP compliance in Mumbai
Mumbai, India

Editions on record

23 Jan 2017
GMP compliance in Mumbai 2017
Organiser
13 Oct 2016
Lymphoma and Myeloma - International Congress on Hematologic Malignancies 2016
Organiser
25 Jul 2016
Cape Town Seminar on Complaint Handling and Management 2016
Organiser
21 Jul 2016
Cape Town Seminar on How to Prepare For and Survive During an FDA Inspection 2016
Organiser
18 Jul 2016
Seminar on Why is FDA at my Facility, and what do I do During an Inspection 2016
Organiser
18 Jul 2016
Seminar on Mastering Biofilm Control, Monitoring, Validation and Excursion Investigations 2016
Organiser
30 Jun 2016
Food Safety & Defense: Key Factors to Safely Manufacture, Package & Handle Food Products 2016
Organiser
30 Jun 2016
Internal Auditing for the Medical Device Industry Seminar 2016
Organiser
23 Jun 2016
2-day In-person Seminar Effective Audit Report Writing 2016
Organiser
23 Jun 2016
2-day In-person Seminar Advanced Payroll 2016
Organiser
23 Jun 2016
Cash Management: A User's Perspective - The How's, Why's and Wherefores 2016
Organiser
16 Jun 2016
2-day In-person Seminar FDA Device Software Regulation 2016
Organiser
16 Jun 2016
2-day In-person Seminar The A to Z's of HIPAA Compliance 2016
Organiser
16 Jun 2016
Applying U.S. FDA Laws and Regulations to Each Phase of Total Product Life Cycle (TPLC) Seminar 2016
Organiser
2 Jun 2016
2-day In-person Seminar Air Traffic Control: How it REALLY works! 2016
Organiser
2 Jun 2016
A Matter of Ethics: Facing the Fear of Doing the Right Thing 2016
Organiser
2 Jun 2016
2-day In-person Seminar Conducting Internal Investigations 2016
Organiser
2 Jun 2016
2-day In-person Seminar Tax and Accounting Strategies for Residential Real Estate Investors 2016
Organiser
3 Dec 2015
2-day In-person Seminar on Validation and Part 11 Compliance of Computer Systems and Data 2015
Organiser
12 Nov 2015
Singapore Conference on Good Manufacturing Practice Compliance for Pharmaceutical Quality 2015
Organiser
5 Nov 2015
HIPAA Privacy Security - Time to Get Serious Conference - Chicago, IL 2015
Organiser
5 Nov 2015
Enterprise Risk Management In The New World Seminar 2015
Organiser
2 Nov 2015
Marketing Products without Getting Hammered by FDA at Zurich, Switzerland 2015
Organiser
19 Oct 2015
The A to Z's of Microbial Control, Monitoring, Validation and Troubleshooting of Pharmaceutical Water Systems 2015
Organiser
19 Oct 2015
The A to Z's of Microbial Control, Monitoring, Validation and Troubleshooting 2015
Organiser
7 Jan 2015
ATC Radar Approach Control (TRACON) 2015
Organiser
6 Jan 2015
GMP Expectations for Products Used in Early Phase IND Studies 2015
Organiser
13 Nov 2014
2-day In-person Seminar on Validation and Part 11/Annex11 2014
Organiser
30 Oct 2014
2day In-person Seminar on “The A to Z's of HIPAA Privacy, Security, and Breach Notification Rules” 2014
Organiser
30 Oct 2014
2-day In-person Seminar on “Combination Products 2014
Organiser
30 Oct 2014
2-day In-person Seminar on “Quality Audits for the Medical Device Industry” 2014
Organiser
30 Oct 2014
2-day In-person Seminar on “The A to Z's of HIPAA Privacy, Security, and Breach Notification Rules” 2014
Organiser
27 Oct 2014
2-day In-person Seminar on "Applying ISO14971:2012 and IEC62304 - A Guide to Practical Risk Management
Organiser
23 Oct 2014
2-day In-person Seminar on “Applying ISO14971:2012 and IEC62304
Organiser
23 Oct 2014
2-day In-person Seminar on “Quality System Regulations for Drugs, Devices, and Tablets 2014
Organiser
16 Oct 2014
Statistical Considerations for ICH Guidelines Seminar 2014
Organiser
9 Oct 2014
The DHF, Technical File and Design Dossier - Similarities, Differences and The Future 2014
Organiser
9 Oct 2014
Seminar on The DHF, Technical File and Design Dossier - Similarities, Differences and the Future 2014
Organiser
2 Oct 2014
2-day In-person Seminar on “Validate Your Own Excel Spreadsheet Application Workshop” 2014
Organiser
18 Sep 2014
2-day In-person Seminar GMP Compliance for Pharmaceutical Quality Control Laboratories 2014
Organiser
15 Sep 2014
GMP Compliance for Pharmaceutical Quality Control Laboratories: 2-day In-person Seminar 2014
Organiser
11 Sep 2014
Live In-Person Seminar on “GMP Compliance for Pharmaceutical Quality Control Laboratories” 2014
Organiser
11 Sep 2014
2-day In-person Seminar on Advanced Course: Validation & 21 CFR 11 Compliance 2014
Organiser
4 Sep 2014
2-day In-person Seminar Global Medical Device Regulations - US, EU and Canada 2014
Organiser
4 Sep 2014
2-day In-person Seminar on Global Medical Device Regulation 2014
Organiser
28 Aug 2014
The DHF, Technical File and Design Dossier - Similarities, Differences and The Future 2014
Organiser
27 Aug 2014
How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare 2014
Organiser
21 Aug 2014
2day Inperson Seminar on FDAs and the US Customs Border Patrols Import 2014
Organiser
21 Aug 2014
The Most Common Problems with Software Validation Processes 2014
Organiser
18 Aug 2014
Measurement Uncertainty in Microbiology 2014
Organiser
14 Aug 2014
How to Get Your Combination Product Approved and onto the US Marketplace Seminar 2014
Organiser
14 Aug 2014
2day Inperson seminar on Combination Products How to Get Your Combination Product Approved 2014
Organiser
12 Aug 2014
ICH GCPs and the Clinical Research Process (Including Phase 0,1,2,3 and Phase 4 trials) 2014
Organiser
12 Aug 2014
Excel Spreadsheet Validation for FDA 21 CFR Part 11 2014
Organiser
8 Aug 2014
Live Seminar: Advertising and Promotional Requirements for Drugs and Medical Devices 2014
Organiser
7 Aug 2014
Advertising and Promotional Requirements for Drugs and Medical Devices 2014
Organiser
7 Aug 2014
2-day In-person Seminar FDA Based Guidelines on Statistical Sampling Plans 2014
Organiser
5 Aug 2014
Key Concepts in Successful Water System Sanitization 2014
Organiser
4 Aug 2014
2-day In-person Seminar Statistical Considerations for ICH Guidelines 2014
Organiser

Is this your company? Send us corrections or list your next event.