SafetyCall International is an independent, professional health care practice licensed by the Boards of Medicine, Pharmacy and Veterinary Medicine, dedicated to providing industries with a suite of product safety-related services to help our clients meet federal regulatory compliance obligations.
Adverse Event Reporting
24/7 management, documentation and assessment of adverse events
Regulatory Compliance
We help companies comply with mandatory adverse event reporting responsibilities in the US and Canada (FDA, EPA, CPSC, and Health Canada).
Pharmacovigilance
SafetyCall clinicians will collect, detect, assess, and monitor adverse effects of pharmaceutical products.
24/7 Medical Contact Center
SafetyCall is a US based contact center delivering product safety solutions.
Trend Analysis & Benchmarking Review
SafetyCall clinicians routinely help clients understand their on-going safety surveillance experience by analyzing and presenting the aggregate adverse event data.
Consulting
With over 40 years’ experience, our medical and veterinary consulting group provides independent, expert review and analysis in the fields of clinical toxicology and product safety.
SafetyCall is a licensed health care practice providing adverse event management services in the pharmaceutical industry.
Your solution for meeting requirements of the Dietary Supplement and Non-Prescription Drug Consumer Protection Act.
The health care professionals at SafetyCall have over 40 years of experience responding to issues related to over the counter medications.
Your solution for meeting the mandatory adverse event reporting requirements of the Modernization of Cosmetics Regulatory Act of 2022 (MoCRA).
SafetyCall is the only licensed adverse event call center that manages both animal and human markets.
SafetyCall professionals manage adverse events and medical information inquiries for the Consumer Product industry.
We manage and report adverse events to help manufacturers comply with Consumer Medical Device Reporting regulations under the FDA.
SafetyCall manages adverse events for companies in the Agricultural Chemicals / Pesticide Industry.
SafetyCall is a licensed health care practice providing adverse incident and adverse event management services in the medical cannabis industry.
There is currently not a clear regulatory pathway for CBD containing products. SafetyCall is supporting Manufacturers following the principles of a Best Practice Post-Market Surveillance System.
We manage and document adverse events and medical information inquiries for the Institutional Product Market complying with FIFRA and TSCA requirements.
We manage and provide documentation of adverse events with industrial chemical contact and help with regulatory reporting to relevant federal agencies.
SafetyCall is a licensed health care practice providing adverse event management services in the pharmaceutical industry.
Learn moreYour solution for meeting requirements of the Dietary Supplement and Non-Prescription Drug Consumer Protection Act.
Learn moreThe health care professionals at SafetyCall have over 40 years of experience responding to issues related to over the counter medications.
Learn moreYour solution for meeting the mandatory adverse event reporting requirements of the Modernization of Cosmetics Regulatory Act of 2022 (MoCRA).
Learn moreSafetyCall is the only licensed adverse event call center that manages both animal and human markets.
Learn moreSafetyCall professionals manage adverse events and medical information inquiries for the Consumer Product industry.
Learn moreWe manage and report adverse events to help manufacturers comply with Consumer Medical Device Reporting regulations under the FDA.
Learn moreSafetyCall manages adverse events for companies in the Agricultural Chemicals / Pesticide Industry.
Learn moreSafetyCall is a licensed health care practice providing adverse incident and adverse event management services in the medical cannabis industry.
Learn moreThere is currently not a clear regulatory pathway for CBD containing products. SafetyCall is supporting Manufacturers following the principles of a Best Practice Post-Market Surveillance System.
Learn moreWe manage and document adverse events and medical information inquiries for the Institutional Product Market complying with FIFRA and TSCA requirements.
Learn moreWe manage and provide documentation of adverse events with industrial chemical contact and help with regulatory reporting to relevant federal agencies.
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