Trainings for FDA Compliance - Webinars, Seminars on Latest Regulations

HIPAA Privacy Rule Compliance-Understanding New Rules and Responsibilities of Privacy Officer

Biocompatibility Testing for Medical Devices

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

PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation

Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs)

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

FDA's GMP Expectations for Phase I and First-in-Man Clinical Trials

Quality Control Laboratory Compliance - cGMPs and GLPs

Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina)

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

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

21 CFR Part 11 Compliance for SaaS/Cloud Applications

Designing and Sustaining New and Existing Product Stability Testing Program

FDA's New Import Program for 2019 - Strict Precision

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Webinars

Streamlining Your Internal Auditing Process

FDA's Ambitious Regulation of Social Media

Annual Current Good Manufacturing Practices (cGMP) Training

The PSMF- Accountability, Inspection Preparation and Business Analytics

Specification and OOS for Pharma, Biopharma and Combination Products

Raw Materials in Pharma/Biotech Production

Access Point Case Management: Managing the 2 Midnight Rule via Your Routes of Entry

Use of Wearable Devices in Clinical Trials

Requirements for Running Clinical Trials in Pediatrics for the EU

Coatings in Medical Devices – ISO 17327

Technical Writing in an Industrial Environment

How to Establish and Maintain a Compliant, Practical Clinical Quality Management System in ....

GxP/GMP Requirements and its Consequences for Documentation and Information Technology Sys ....

Orphan Drug Development History & Overview

The Impact of ICH E6 R2

Seminars

HIPAA Privacy Rule Compliance-Understanding New Rules and Responsibilities of Privacy Officer

Biocompatibility Testing for Medical Devices

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

PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation

Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs)

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

FDA's GMP Expectations for Phase I and First-in-Man Clinical Trials

Quality Control Laboratory Compliance - cGMPs and GLPs

Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina)

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

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

21 CFR Part 11 Compliance for SaaS/Cloud Applications

Designing and Sustaining New and Existing Product Stability Testing Program

FDA's New Import Program for 2019 - Strict Precision

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