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Imagem principal de REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

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Imagem principal de Global Regulatory Requirements for Drug Safety & Pharmacovigilance

Global Regulatory Requirements for Drug Safety & Pharmacovigilance

Tue, May 14, 12:30 PM GMT+5:30

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Imagem principal de Project Management Essentials For Non-Project Managers Training Course

Project Management Essentials For Non-Project Managers Training Course

Wed, May 15, 12:00 PM GMT+5:30

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Imagem principal de Risk Management for Medical Devices per ISO 14971

Risk Management for Medical Devices per ISO 14971

Thu, May 16, 1:00 PM GMT+5:30

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Imagem principal de Drug Development: Key to Success from Concept to Commercialization

Drug Development: Key to Success from Concept to Commercialization

Wed, May 22, 12:30 PM GMT+5:30

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Imagem principal de Supplier and Contract Manufacturer Management

Supplier and Contract Manufacturer Management

Sat, May 25, 9:00 AM EDT

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Imagem principal de Biostatistics for the Non-Statistician Training Course

Biostatistics for the Non-Statistician Training Course

Wed, May 29, 12:00 PM GMT+5:30

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Imagem principal de Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based App

Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based App

Wed, May 29, 12:30 PM GMT+5:30

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Imagem principal de CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectation

CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectation

Wed, May 29, 1:00 PM GMT+5:30

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Imagem principal de GMP Compliance for Quality Control and Laboratory Operations

GMP Compliance for Quality Control and Laboratory Operations

Tue, Jun 4, 12:00 PM GMT+5:30

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Imagem principal de Developing the Master V&V Plan to Meet U.S. FDA, ISO 13485 and 14971

Developing the Master V&V Plan to Meet U.S. FDA, ISO 13485 and 14971

Wed, Jun 12, 10:00 AM GMT+5:30

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Imagem principal de REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

segunda-feira às 10:00 GMT+5:30

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Imagem principal de Global Regulatory Requirements for Drug Safety & Pharmacovigilance

Global Regulatory Requirements for Drug Safety & Pharmacovigilance

Tue, May 14, 12:30 PM GMT+5:30

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Imagem principal de Project Management Essentials For Non-Project Managers Training Course

Project Management Essentials For Non-Project Managers Training Course

Wed, May 15, 12:00 PM GMT+5:30

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Imagem principal de Risk Management for Medical Devices per ISO 14971

Risk Management for Medical Devices per ISO 14971

Thu, May 16, 1:00 PM GMT+5:30

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Imagem principal de Drug Development: Key to Success from Concept to Commercialization

Drug Development: Key to Success from Concept to Commercialization

Wed, May 22, 12:30 PM GMT+5:30

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Imagem principal de Supplier and Contract Manufacturer Management

Supplier and Contract Manufacturer Management

Sat, May 25, 9:00 AM EDT

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Imagem principal de Biostatistics for the Non-Statistician Training Course

Biostatistics for the Non-Statistician Training Course

Wed, May 29, 12:00 PM GMT+5:30

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Imagem principal de Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based App

Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based App

Wed, May 29, 12:30 PM GMT+5:30

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Imagem principal de CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectation

CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectation

Wed, May 29, 1:00 PM GMT+5:30

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Imagem principal de GMP Compliance for Quality Control and Laboratory Operations

GMP Compliance for Quality Control and Laboratory Operations

Tue, Jun 4, 12:00 PM GMT+5:30

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Imagem principal de Developing the Master V&V Plan to Meet U.S. FDA, ISO 13485 and 14971

Developing the Master V&V Plan to Meet U.S. FDA, ISO 13485 and 14971

Wed, Jun 12, 10:00 AM GMT+5:30

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Passados (1.5K)

Imagem principal de DHF, DMR, DHR, Technical Documentation for US FDA, ISO and EU MDR

DHF, DMR, DHR, Technical Documentation for US FDA, ISO and EU MDR

Tue, Apr 30, 1:00 PM EDT

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Imagem principal de FDA Recalls - Before You Start, and After You Finish

FDA Recalls - Before You Start, and After You Finish

Mon, Apr 29, 10:00 AM EDT

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Imagem principal de Validation of FDA-Regulated Systems that Incorporate Artificial Intelligenc

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligenc

Thu, Apr 25, 1:00 PM EDT

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Imagem principal de cGMP Training on FDA Inspections – A webinar to understand FDA, EMA

cGMP Training on FDA Inspections – A webinar to understand FDA, EMA

Thu, Apr 25, 1:00 PM GMT+5:30

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Imagem principal de Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud

Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud

Tue, Apr 23, 11:00 AM EDT

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Imagem principal de Writing and Implementing SOP in Laboratory for FDA, EPA, and OSHA Complianc

Writing and Implementing SOP in Laboratory for FDA, EPA, and OSHA Complianc

Mon, Apr 22, 12:30 PM EDT

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Imagem principal de Useful Statistical Methods for Defining Product and Process Specifications

Useful Statistical Methods for Defining Product and Process Specifications

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Imagem principal de Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FD

Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FD

Tue, Apr 16, 1:00 PM EDT

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Imagem principal de Achieving Compliance for FDA-Regulated Systems by Following Principles of C

Achieving Compliance for FDA-Regulated Systems by Following Principles of C

Thu, Apr 4, 1:00 PM GMT+5:30

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Imagem principal de Device Changes, FDA Changes, and the 510(k)

Device Changes, FDA Changes, and the 510(k)

Tue, Apr 2, 1:00 PM GMT+5:30

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Imagem principal de FDA's Latest Guidance for Cybersecurity for Medical Devices: Quality Manage

FDA's Latest Guidance for Cybersecurity for Medical Devices: Quality Manage

Wed, Mar 27, 1:00 PM EDT

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Imagem principal de GMP Compliance for Quality Control and Laboratory Operations

GMP Compliance for Quality Control and Laboratory Operations

Mon, Mar 25, 12:00 PM EDT

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Imagem principal de DHF, DMR, DHR, Technical Documentation for US FDA, ISO and EU MDR

DHF, DMR, DHR, Technical Documentation for US FDA, ISO and EU MDR

Tue, Apr 30, 1:00 PM EDT

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Imagem principal de FDA Recalls - Before You Start, and After You Finish

FDA Recalls - Before You Start, and After You Finish

Mon, Apr 29, 10:00 AM EDT

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Imagem principal de Validation of FDA-Regulated Systems that Incorporate Artificial Intelligenc

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligenc

Thu, Apr 25, 1:00 PM EDT

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Imagem principal de cGMP Training on FDA Inspections – A webinar to understand FDA, EMA

cGMP Training on FDA Inspections – A webinar to understand FDA, EMA

Thu, Apr 25, 1:00 PM GMT+5:30

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Imagem principal de Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud

Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud

Tue, Apr 23, 11:00 AM EDT

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Imagem principal de Writing and Implementing SOP in Laboratory for FDA, EPA, and OSHA Complianc

Writing and Implementing SOP in Laboratory for FDA, EPA, and OSHA Complianc

Mon, Apr 22, 12:30 PM EDT

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Imagem principal de Useful Statistical Methods for Defining Product and Process Specifications

Useful Statistical Methods for Defining Product and Process Specifications

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Imagem principal de Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FD

Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FD

Tue, Apr 16, 1:00 PM EDT

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Imagem principal de Achieving Compliance for FDA-Regulated Systems by Following Principles of C

Achieving Compliance for FDA-Regulated Systems by Following Principles of C

Thu, Apr 4, 1:00 PM GMT+5:30

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Imagem principal de Device Changes, FDA Changes, and the 510(k)

Device Changes, FDA Changes, and the 510(k)

Tue, Apr 2, 1:00 PM GMT+5:30

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Imagem principal de FDA's Latest Guidance for Cybersecurity for Medical Devices: Quality Manage

FDA's Latest Guidance for Cybersecurity for Medical Devices: Quality Manage

Wed, Mar 27, 1:00 PM EDT

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Imagem principal de GMP Compliance for Quality Control and Laboratory Operations

GMP Compliance for Quality Control and Laboratory Operations

Mon, Mar 25, 12:00 PM EDT

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Eventos

Imagem principal de REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

segunda-feira às 10:00 GMT+5:30

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Imagem principal de Global Regulatory Requirements for Drug Safety & Pharmacovigilance

Global Regulatory Requirements for Drug Safety & Pharmacovigilance

Tue, May 14, 12:30 PM GMT+5:30

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Imagem principal de Project Management Essentials For Non-Project Managers Training Course

Project Management Essentials For Non-Project Managers Training Course

Wed, May 15, 12:00 PM GMT+5:30

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Imagem principal de Risk Management for Medical Devices per ISO 14971

Risk Management for Medical Devices per ISO 14971

Thu, May 16, 1:00 PM GMT+5:30

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Imagem principal de Drug Development: Key to Success from Concept to Commercialization

Drug Development: Key to Success from Concept to Commercialization

Wed, May 22, 12:30 PM GMT+5:30

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Imagem principal de Supplier and Contract Manufacturer Management

Supplier and Contract Manufacturer Management

Sat, May 25, 9:00 AM EDT

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Imagem principal de Biostatistics for the Non-Statistician Training Course

Biostatistics for the Non-Statistician Training Course

Wed, May 29, 12:00 PM GMT+5:30

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Imagem principal de Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based App

Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based App

Wed, May 29, 12:30 PM GMT+5:30

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Imagem principal de CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectation

CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectation

Wed, May 29, 1:00 PM GMT+5:30

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Imagem principal de GMP Compliance for Quality Control and Laboratory Operations

GMP Compliance for Quality Control and Laboratory Operations

Tue, Jun 4, 12:00 PM GMT+5:30

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Imagem principal de Developing the Master V&V Plan to Meet U.S. FDA, ISO 13485 and 14971

Developing the Master V&V Plan to Meet U.S. FDA, ISO 13485 and 14971

Wed, Jun 12, 10:00 AM GMT+5:30

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Imagem principal de REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

segunda-feira às 10:00 GMT+5:30

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Imagem principal de Global Regulatory Requirements for Drug Safety & Pharmacovigilance

Global Regulatory Requirements for Drug Safety & Pharmacovigilance

Tue, May 14, 12:30 PM GMT+5:30

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Imagem principal de Project Management Essentials For Non-Project Managers Training Course

Project Management Essentials For Non-Project Managers Training Course

Wed, May 15, 12:00 PM GMT+5:30

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Imagem principal de Risk Management for Medical Devices per ISO 14971

Risk Management for Medical Devices per ISO 14971

Thu, May 16, 1:00 PM GMT+5:30

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Imagem principal de Drug Development: Key to Success from Concept to Commercialization

Drug Development: Key to Success from Concept to Commercialization

Wed, May 22, 12:30 PM GMT+5:30

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Imagem principal de Supplier and Contract Manufacturer Management

Supplier and Contract Manufacturer Management

Sat, May 25, 9:00 AM EDT

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Imagem principal de Biostatistics for the Non-Statistician Training Course

Biostatistics for the Non-Statistician Training Course

Wed, May 29, 12:00 PM GMT+5:30

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Imagem principal de Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based App

Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based App

Wed, May 29, 12:30 PM GMT+5:30

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Imagem principal de CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectation

CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectation

Wed, May 29, 1:00 PM GMT+5:30

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Imagem principal de GMP Compliance for Quality Control and Laboratory Operations

GMP Compliance for Quality Control and Laboratory Operations

Tue, Jun 4, 12:00 PM GMT+5:30

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Imagem principal de Developing the Master V&V Plan to Meet U.S. FDA, ISO 13485 and 14971

Developing the Master V&V Plan to Meet U.S. FDA, ISO 13485 and 14971

Wed, Jun 12, 10:00 AM GMT+5:30

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Imagem principal de DHF, DMR, DHR, Technical Documentation for US FDA, ISO and EU MDR

DHF, DMR, DHR, Technical Documentation for US FDA, ISO and EU MDR

Tue, Apr 30, 1:00 PM EDT

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Imagem principal de FDA Recalls - Before You Start, and After You Finish

FDA Recalls - Before You Start, and After You Finish

Mon, Apr 29, 10:00 AM EDT

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Imagem principal de Validation of FDA-Regulated Systems that Incorporate Artificial Intelligenc

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligenc

Thu, Apr 25, 1:00 PM EDT

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Imagem principal de cGMP Training on FDA Inspections – A webinar to understand FDA, EMA

cGMP Training on FDA Inspections – A webinar to understand FDA, EMA

Thu, Apr 25, 1:00 PM GMT+5:30

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Imagem principal de Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud

Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud

Tue, Apr 23, 11:00 AM EDT

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Imagem principal de Writing and Implementing SOP in Laboratory for FDA, EPA, and OSHA Complianc

Writing and Implementing SOP in Laboratory for FDA, EPA, and OSHA Complianc

Mon, Apr 22, 12:30 PM EDT

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Imagem principal de Useful Statistical Methods for Defining Product and Process Specifications

Useful Statistical Methods for Defining Product and Process Specifications

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Imagem principal de Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FD

Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FD

Tue, Apr 16, 1:00 PM EDT

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Imagem principal de Achieving Compliance for FDA-Regulated Systems by Following Principles of C

Achieving Compliance for FDA-Regulated Systems by Following Principles of C

Thu, Apr 4, 1:00 PM GMT+5:30

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Imagem principal de Device Changes, FDA Changes, and the 510(k)

Device Changes, FDA Changes, and the 510(k)

Tue, Apr 2, 1:00 PM GMT+5:30

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Imagem principal de FDA's Latest Guidance for Cybersecurity for Medical Devices: Quality Manage

FDA's Latest Guidance for Cybersecurity for Medical Devices: Quality Manage

Wed, Mar 27, 1:00 PM EDT

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Imagem principal de GMP Compliance for Quality Control and Laboratory Operations

GMP Compliance for Quality Control and Laboratory Operations

Mon, Mar 25, 12:00 PM EDT

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Imagem principal de DHF, DMR, DHR, Technical Documentation for US FDA, ISO and EU MDR

DHF, DMR, DHR, Technical Documentation for US FDA, ISO and EU MDR

Tue, Apr 30, 1:00 PM EDT

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Imagem principal de FDA Recalls - Before You Start, and After You Finish

FDA Recalls - Before You Start, and After You Finish

Mon, Apr 29, 10:00 AM EDT

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Imagem principal de Validation of FDA-Regulated Systems that Incorporate Artificial Intelligenc

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligenc

Thu, Apr 25, 1:00 PM EDT

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Imagem principal de cGMP Training on FDA Inspections – A webinar to understand FDA, EMA

cGMP Training on FDA Inspections – A webinar to understand FDA, EMA

Thu, Apr 25, 1:00 PM GMT+5:30

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Imagem principal de Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud

Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud

Tue, Apr 23, 11:00 AM EDT

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Imagem principal de Writing and Implementing SOP in Laboratory for FDA, EPA, and OSHA Complianc

Writing and Implementing SOP in Laboratory for FDA, EPA, and OSHA Complianc

Mon, Apr 22, 12:30 PM EDT

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Imagem principal de Useful Statistical Methods for Defining Product and Process Specifications

Useful Statistical Methods for Defining Product and Process Specifications

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Imagem principal de Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FD

Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FD

Tue, Apr 16, 1:00 PM EDT

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Imagem principal de Achieving Compliance for FDA-Regulated Systems by Following Principles of C

Achieving Compliance for FDA-Regulated Systems by Following Principles of C

Thu, Apr 4, 1:00 PM GMT+5:30

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Imagem principal de Device Changes, FDA Changes, and the 510(k)

Device Changes, FDA Changes, and the 510(k)

Tue, Apr 2, 1:00 PM GMT+5:30

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Imagem principal de FDA's Latest Guidance for Cybersecurity for Medical Devices: Quality Manage

FDA's Latest Guidance for Cybersecurity for Medical Devices: Quality Manage

Wed, Mar 27, 1:00 PM EDT

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Imagem principal de GMP Compliance for Quality Control and Laboratory Operations

GMP Compliance for Quality Control and Laboratory Operations

Mon, Mar 25, 12:00 PM EDT

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