Trainings for FDA Compliance - Webinars, Seminars on Latest Regulations

Preparing for FDA's New Import/Export Trauma in 2020

Biostatistics for the Non-Statistician

FDA Recalls - Before You Start, and After You Finish

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

Quality Control Laboratory Compliance - cGMPs and GLPs

Building a Vendor Qualification Program for FDA Regulated Industries

Beyond NanoEHS Risk Assessments - Leading at the Interface of Science and Business

Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry (Pharmaceuticals, Biologics, Medical Devic ....

Designing and Sustaining New and Existing Product Stability Testing Program

Equipment and Utilities Qualification

Biocompatibility Testing for Medical Devices

Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection

Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices

REACH and RoHS Compliance: Gain a Deeper Understanding

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Webinars

USDA New Proposed Rule on BioEngineered (GMO) Food Disclosure

Complaint Handling Requirements (US); Interrelationship with CAPA, Change Control, Adverse ....

Steam Sterilization Microbiology and Autoclave Performance Qualification

A Global Review of Regulations Applied to Spices, Herbs and Flavors

How Sponsors Generate GCP Noncompliance at Investigator Sites

Seminars

Preparing for FDA's New Import/Export Trauma in 2020

Biostatistics for the Non-Statistician

FDA Recalls - Before You Start, and After You Finish

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

Quality Control Laboratory Compliance - cGMPs and GLPs

Building a Vendor Qualification Program for FDA Regulated Industries

Beyond NanoEHS Risk Assessments - Leading at the Interface of Science and Business

Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry (Pharmaceuticals, Biologics, Medical Devic ....

Designing and Sustaining New and Existing Product Stability Testing Program

Equipment and Utilities Qualification

Biocompatibility Testing for Medical Devices

Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection

Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices

REACH and RoHS Compliance: Gain a Deeper Understanding

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