Overview
About AmoSey Inc.
AmoSey Inc. - Pharmaceutical/ Biologics/ Medical Devices/ NHP Regulatory, Quality Compliance and Pharmacovigilance Consultancy
Based in Toronto, Canada, AmoSey Inc. is a healthcare consultancy with extensive regulatory, quality and compliance, and pharmacovigilance experience. At AmoSey Inc we are dedicated to providing cost effective yet quality and efficient solutions. We take pride in performing regulatory filings, QA and Pharmacovigilance activities for products ranging from well established health care products to some of the novel technology products like liposomes, complex formulations, vaccines and new medical devices. We also offer Translation services in >30 languages. Our team of highly skilled and qualified professionals have hands on experience in providing regulatory and quality solutions in:
Drug Products, Biologics and Vaccines
Natural Health Products
Medical Devices
Veterinary drugs
OTC's
Disinfectants and Pesticides
Clinical Research/ Clinical Trial Applications/ IND
Product Life-Cycle Management
Product Conformance
Data Integrity
Gap Analysis and Remediation
Patent Infirngement
GMP Audits, Compliance and Training
Deviations and Failure investigation
Complaint Handling and Recall
CMC Change Management
Risk Management
SOP's and Documentation
ADR Reporting
Product development
ISO 13485: 2016, MDSAP and ISO 9001
Qualification and Validation
Based in Toronto, Canada, AmoSey Inc. is a healthcare consultancy with extensive regulatory, quality and compliance, and pharmacovigilance experience. At AmoSey Inc we are dedicated to providing cost effective yet quality and efficient solutions. We take pride in performing regulatory filings, QA and Pharmacovigilance activities for products ranging from well established health care products to some of the novel technology products like liposomes, complex formulations, vaccines and new medical devices. We also offer Translation services in >30 languages. Our team of highly skilled and qualified professionals have hands on experience in providing regulatory and quality solutions in:
Drug Products, Biologics and Vaccines
Natural Health Products
Medical Devices
Veterinary drugs
OTC's
Disinfectants and Pesticides
Clinical Research/ Clinical Trial Applications/ IND
Product Life-Cycle Management
Product Conformance
Data Integrity
Gap Analysis and Remediation
Patent Infirngement
GMP Audits, Compliance and Training
Deviations and Failure investigation
Complaint Handling and Recall
CMC Change Management
Risk Management
SOP's and Documentation
ADR Reporting
Product development
ISO 13485: 2016, MDSAP and ISO 9001
Qualification and Validation