worldcomplianceseminars

Upcoming (15)

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

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

Monday • 12:30 PM EDT

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

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

Tuesday • 11:00 AM EDT

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

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

Thursday • 1:00 PM GMT+5:30

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Validation of FDA-Regulated Systems that Incorporate Artificial Intelligenc primary image

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligenc

Thursday • 1:00 PM EDT

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FDA Recalls - Before You Start, and After You Finish primary image

FDA Recalls - Before You Start, and After You Finish

Mon, Apr 29 • 10:00 AM EDT

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

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

Tue, Apr 30 • 1:00 PM EDT

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REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance primary image

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

Mon, May 6 • 10:00 AM GMT+5:30

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Global Regulatory Requirements for Drug Safety & Pharmacovigilance primary image

Global Regulatory Requirements for Drug Safety & Pharmacovigilance

Tue, May 14 • 12:30 PM GMT+5:30

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Project Management Essentials For Non-Project Managers Training Course primary image

Project Management Essentials For Non-Project Managers Training Course

Wed, May 15 • 12:00 PM GMT+5:30

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Risk Management for Medical Devices per ISO 14971 primary image

Risk Management for Medical Devices per ISO 14971

Thu, May 16 • 1:00 PM GMT+5:30

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Drug Development: Key to Success from Concept to Commercialization primary image

Drug Development: Key to Success from Concept to Commercialization

Wed, May 22 • 12:30 PM GMT+5:30

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Supplier and Contract Manufacturer Management primary image

Supplier and Contract Manufacturer Management

Sat, May 25 • 9:00 AM EDT

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

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

Monday • 12:30 PM EDT

Check ticket price on event

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

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

Tuesday • 11:00 AM EDT

Check ticket price on event

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

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

Thursday • 1:00 PM GMT+5:30

Check ticket price on event

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligenc primary image

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligenc

Thursday • 1:00 PM EDT

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FDA Recalls - Before You Start, and After You Finish primary image

FDA Recalls - Before You Start, and After You Finish

Mon, Apr 29 • 10:00 AM EDT

Check ticket price on event

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

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

Tue, Apr 30 • 1:00 PM EDT

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REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance primary image

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

Mon, May 6 • 10:00 AM GMT+5:30

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Global Regulatory Requirements for Drug Safety & Pharmacovigilance primary image

Global Regulatory Requirements for Drug Safety & Pharmacovigilance

Tue, May 14 • 12:30 PM GMT+5:30

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Project Management Essentials For Non-Project Managers Training Course primary image

Project Management Essentials For Non-Project Managers Training Course

Wed, May 15 • 12:00 PM GMT+5:30

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Risk Management for Medical Devices per ISO 14971 primary image

Risk Management for Medical Devices per ISO 14971

Thu, May 16 • 1:00 PM GMT+5:30

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Drug Development: Key to Success from Concept to Commercialization primary image

Drug Development: Key to Success from Concept to Commercialization

Wed, May 22 • 12:30 PM GMT+5:30

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Supplier and Contract Manufacturer Management primary image

Supplier and Contract Manufacturer Management

Sat, May 25 • 9:00 AM EDT

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Past (1.5K)

Useful Statistical Methods for Defining Product and Process Specifications primary image

Useful Statistical Methods for Defining Product and Process Specifications

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

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

Tue, Apr 16 • 1:00 PM EDT

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

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

Thu, Apr 4 • 1:00 PM GMT+5:30

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

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

Tue, Apr 2 • 1:00 PM GMT+5:30

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

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

Wed, Mar 27 • 1:00 PM EDT

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GMP Compliance for Quality Control and Laboratory Operations primary image

GMP Compliance for Quality Control and Laboratory Operations

Mon, Mar 25 • 12:00 PM EDT

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FDA & OSHA Warehouse Requirements Training Course primary image

FDA & OSHA Warehouse Requirements Training Course

Tue, Mar 19 • 1:00 PM EDT

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Pharmaceutical Document Management Training Course - A Global Regulatory primary image

Pharmaceutical Document Management Training Course - A Global Regulatory

Tue, Mar 19 • 12:00 PM EDT

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Writing and Enforcing SOPs: Best Practices for Regulated Industries primary image

Writing and Enforcing SOPs: Best Practices for Regulated Industries

Mon, Mar 18 • 12:30 PM EDT

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Aseptic Processing Of Pharmaceutical and Biotech Products primary image

Aseptic Processing Of Pharmaceutical and Biotech Products

Mon, Mar 18 • 12:30 PM EDT

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Design History File (DHF), Device Master Record (DMR), and Device History R primary image

Design History File (DHF), Device Master Record (DMR), and Device History R

Mon, Mar 18 • 12:00 PM EDT

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The 6 Most Common Problems in FDA Software Validation and Verification - Ne primary image

The 6 Most Common Problems in FDA Software Validation and Verification - Ne

Thu, Mar 14 • 1:00 AM EDT

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Useful Statistical Methods for Defining Product and Process Specifications primary image

Useful Statistical Methods for Defining Product and Process Specifications

Check ticket price on event

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

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

Tue, Apr 16 • 1:00 PM EDT

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

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

Thu, Apr 4 • 1:00 PM GMT+5:30

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

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

Tue, Apr 2 • 1:00 PM GMT+5:30

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

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

Wed, Mar 27 • 1:00 PM EDT

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GMP Compliance for Quality Control and Laboratory Operations primary image

GMP Compliance for Quality Control and Laboratory Operations

Mon, Mar 25 • 12:00 PM EDT

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FDA & OSHA Warehouse Requirements Training Course primary image

FDA & OSHA Warehouse Requirements Training Course

Tue, Mar 19 • 1:00 PM EDT

Check ticket price on event

Pharmaceutical Document Management Training Course - A Global Regulatory primary image

Pharmaceutical Document Management Training Course - A Global Regulatory

Tue, Mar 19 • 12:00 PM EDT

Check ticket price on event

Writing and Enforcing SOPs: Best Practices for Regulated Industries primary image

Writing and Enforcing SOPs: Best Practices for Regulated Industries

Mon, Mar 18 • 12:30 PM EDT

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Aseptic Processing Of Pharmaceutical and Biotech Products primary image

Aseptic Processing Of Pharmaceutical and Biotech Products

Mon, Mar 18 • 12:30 PM EDT

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Design History File (DHF), Device Master Record (DMR), and Device History R primary image

Design History File (DHF), Device Master Record (DMR), and Device History R

Mon, Mar 18 • 12:00 PM EDT

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The 6 Most Common Problems in FDA Software Validation and Verification - Ne primary image

The 6 Most Common Problems in FDA Software Validation and Verification - Ne

Thu, Mar 14 • 1:00 AM EDT

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Events

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

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

Monday • 12:30 PM EDT

Check ticket price on event

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

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

Tuesday • 11:00 AM EDT

Check ticket price on event

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

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

Thursday • 1:00 PM GMT+5:30

Check ticket price on event

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligenc primary image

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligenc

Thursday • 1:00 PM EDT

Check ticket price on event

FDA Recalls - Before You Start, and After You Finish primary image

FDA Recalls - Before You Start, and After You Finish

Mon, Apr 29 • 10:00 AM EDT

Check ticket price on event

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

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

Tue, Apr 30 • 1:00 PM EDT

Check ticket price on event

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance primary image

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

Mon, May 6 • 10:00 AM GMT+5:30

Check ticket price on event

Global Regulatory Requirements for Drug Safety & Pharmacovigilance primary image

Global Regulatory Requirements for Drug Safety & Pharmacovigilance

Tue, May 14 • 12:30 PM GMT+5:30

Check ticket price on event

Project Management Essentials For Non-Project Managers Training Course primary image

Project Management Essentials For Non-Project Managers Training Course

Wed, May 15 • 12:00 PM GMT+5:30

Check ticket price on event

Risk Management for Medical Devices per ISO 14971 primary image

Risk Management for Medical Devices per ISO 14971

Thu, May 16 • 1:00 PM GMT+5:30

Check ticket price on event

Drug Development: Key to Success from Concept to Commercialization primary image

Drug Development: Key to Success from Concept to Commercialization

Wed, May 22 • 12:30 PM GMT+5:30

Check ticket price on event

Supplier and Contract Manufacturer Management primary image

Supplier and Contract Manufacturer Management

Sat, May 25 • 9:00 AM EDT

Check ticket price on event

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

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

Monday • 12:30 PM EDT

Check ticket price on event

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

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

Tuesday • 11:00 AM EDT

Check ticket price on event

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

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

Thursday • 1:00 PM GMT+5:30

Check ticket price on event

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligenc primary image

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligenc

Thursday • 1:00 PM EDT

Check ticket price on event

FDA Recalls - Before You Start, and After You Finish primary image

FDA Recalls - Before You Start, and After You Finish

Mon, Apr 29 • 10:00 AM EDT

Check ticket price on event

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

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

Tue, Apr 30 • 1:00 PM EDT

Check ticket price on event

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance primary image

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

Mon, May 6 • 10:00 AM GMT+5:30

Check ticket price on event

Global Regulatory Requirements for Drug Safety & Pharmacovigilance primary image

Global Regulatory Requirements for Drug Safety & Pharmacovigilance

Tue, May 14 • 12:30 PM GMT+5:30

Check ticket price on event

Project Management Essentials For Non-Project Managers Training Course primary image

Project Management Essentials For Non-Project Managers Training Course

Wed, May 15 • 12:00 PM GMT+5:30

Check ticket price on event

Risk Management for Medical Devices per ISO 14971 primary image

Risk Management for Medical Devices per ISO 14971

Thu, May 16 • 1:00 PM GMT+5:30

Check ticket price on event

Drug Development: Key to Success from Concept to Commercialization primary image

Drug Development: Key to Success from Concept to Commercialization

Wed, May 22 • 12:30 PM GMT+5:30

Check ticket price on event

Supplier and Contract Manufacturer Management primary image

Supplier and Contract Manufacturer Management

Sat, May 25 • 9:00 AM EDT

Check ticket price on event

Useful Statistical Methods for Defining Product and Process Specifications primary image

Useful Statistical Methods for Defining Product and Process Specifications

Check ticket price on event

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

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

Tue, Apr 16 • 1:00 PM EDT

Check ticket price on event

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

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

Thu, Apr 4 • 1:00 PM GMT+5:30

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

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

Tue, Apr 2 • 1:00 PM GMT+5:30

Check ticket price on event

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

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

Wed, Mar 27 • 1:00 PM EDT

Check ticket price on event

GMP Compliance for Quality Control and Laboratory Operations primary image

GMP Compliance for Quality Control and Laboratory Operations

Mon, Mar 25 • 12:00 PM EDT

Check ticket price on event

FDA & OSHA Warehouse Requirements Training Course primary image

FDA & OSHA Warehouse Requirements Training Course

Tue, Mar 19 • 1:00 PM EDT

Check ticket price on event

Pharmaceutical Document Management Training Course - A Global Regulatory primary image

Pharmaceutical Document Management Training Course - A Global Regulatory

Tue, Mar 19 • 12:00 PM EDT

Check ticket price on event

Writing and Enforcing SOPs: Best Practices for Regulated Industries primary image

Writing and Enforcing SOPs: Best Practices for Regulated Industries

Mon, Mar 18 • 12:30 PM EDT

Check ticket price on event

Aseptic Processing Of Pharmaceutical and Biotech Products primary image

Aseptic Processing Of Pharmaceutical and Biotech Products

Mon, Mar 18 • 12:30 PM EDT

Check ticket price on event

Design History File (DHF), Device Master Record (DMR), and Device History R primary image

Design History File (DHF), Device Master Record (DMR), and Device History R

Mon, Mar 18 • 12:00 PM EDT

Check ticket price on event

The 6 Most Common Problems in FDA Software Validation and Verification - Ne primary image

The 6 Most Common Problems in FDA Software Validation and Verification - Ne

Thu, Mar 14 • 1:00 AM EDT

Check ticket price on event

Useful Statistical Methods for Defining Product and Process Specifications primary image

Useful Statistical Methods for Defining Product and Process Specifications

Check ticket price on event

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

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

Tue, Apr 16 • 1:00 PM EDT

Check ticket price on event

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

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

Thu, Apr 4 • 1:00 PM GMT+5:30

Check ticket price on event

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

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

Tue, Apr 2 • 1:00 PM GMT+5:30

Check ticket price on event

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

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

Wed, Mar 27 • 1:00 PM EDT

Check ticket price on event

GMP Compliance for Quality Control and Laboratory Operations primary image

GMP Compliance for Quality Control and Laboratory Operations

Mon, Mar 25 • 12:00 PM EDT

Check ticket price on event

FDA & OSHA Warehouse Requirements Training Course primary image

FDA & OSHA Warehouse Requirements Training Course

Tue, Mar 19 • 1:00 PM EDT

Check ticket price on event

Pharmaceutical Document Management Training Course - A Global Regulatory primary image

Pharmaceutical Document Management Training Course - A Global Regulatory

Tue, Mar 19 • 12:00 PM EDT

Check ticket price on event

Writing and Enforcing SOPs: Best Practices for Regulated Industries primary image

Writing and Enforcing SOPs: Best Practices for Regulated Industries

Mon, Mar 18 • 12:30 PM EDT

Check ticket price on event

Aseptic Processing Of Pharmaceutical and Biotech Products primary image

Aseptic Processing Of Pharmaceutical and Biotech Products

Mon, Mar 18 • 12:30 PM EDT

Check ticket price on event

Design History File (DHF), Device Master Record (DMR), and Device History R primary image

Design History File (DHF), Device Master Record (DMR), and Device History R

Mon, Mar 18 • 12:00 PM EDT

Check ticket price on event

The 6 Most Common Problems in FDA Software Validation and Verification - Ne primary image

The 6 Most Common Problems in FDA Software Validation and Verification - Ne

Thu, Mar 14 • 1:00 AM EDT

Check ticket price on event