Trainings for FDA Compliance - Webinars, Seminars on Latest Regulations

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

21 CFR Part 11 Compliance for SaaS/Cloud Applications

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

REACH and RoHS Compliance: Gain a Deeper Understanding

FDA's New Import Program for 2019 - Strict Precision

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

Designing and Sustaining New and Existing Product Stability Testing Program

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)

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)

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Webinars

New Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D an ....

Secure Medical Device Procurement

Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certificati ....

CDISC Mapping 3: Compare and Contrast SDTM and ADaM Steps

Supplier and Service Provider Controls: FDA Expectations

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

Consents and 42 CFR Part 2 - New Rules for Re-Release of Substance Use Disorder Informatio ....

Avoidable Delay Management: How to Take Control of Your Length of Stay

Coatings in Medical Devices – ISO 17327

Seminars

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

21 CFR Part 11 Compliance for SaaS/Cloud Applications

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

REACH and RoHS Compliance: Gain a Deeper Understanding

FDA's New Import Program for 2019 - Strict Precision

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

Designing and Sustaining New and Existing Product Stability Testing Program

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)

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)

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