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Webinar On - FDAs 21 CFR Part 11 Add-on Inspections (Canada)

Webinar On - Good Documentation Practices for Clinical Trials (Canada)

Webinar On - How to Develop a Master Validation Plan (Canada)

Webinar On - How to select Software for a Regulated Environment (Online, Canada)

Webinar On - How to withstand an FDA audit of your facilities: A primer for clinical sites, manufacturing facilities and labs (Online, Canada)

Webinar On - HR Leadership Competencies for a Sustainable Future (Canada)

Webinar On - ICH Q10 Pharmaceutical Quality System (Canada)

Webinar On - If It Wasnt Documented It Didnt Happen: Legal & Effective Discipline & Documentation (5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Ca)

Webinar On - Improved Generic Drugs via the 505(b)(2) Regulatory Pathway: FDA Approval Made Easy (Online, Canada)

Webinar On - Introduction to Measurement System Analysis (MSA) (Online, Canada)

Webinar On - Introduction to Process Capability (Canada)

Webinar On - Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs) (5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Ca)

Webinar On - Key Regulatory Documents: Design History File (DHF), Device Master Record (DMR), Device History Record (DHR) and Technical File (TF) and Design Dossier (5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Ca)

Webinar On - Legal and Effective Hiring and Interviewing (Online, Canada)

Webinar On - Managing the FDA form "483": Inspection Observations (Canada)

Webinar On - Master Validation Planning To Meet U.S. FDA cGMP, ISO 13485, and ICH Q9 / ISO 14971 Requirements (Online, Canada)

Webinar On - Medical Devices Designing with Cleanliness in Mind (Online Live Webinar)

Webinar On - Pay Strategy and Performance Management (Online Live Webinar)

Webinar On - Submitting FDA Electronic Regulatory Filings Drug Establishment Registrations and Drug Listings (Canada)

Webinar On - The FDA 510(k): Q-Submission, Preparation and Submission (Online, Canada)