Pharmacovigilance Services
Improving the health and safety of patients is our mission here at Clynico Consulting. We work with your team to ensure that clinical trials done at your sites are conducted in such a way that follows study protocols and local/international regulations.
Clinical Trial Site Services
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Pharmacovigilance Services
Pharmacovigilance Services
Pharmacovigilance Services
Clinical Trial Site Services
Pharmacovigilance Services
Pharmacovigilance Services
Pharmacovigilance Services
Clinical Trial Site Services
Welcome To Clynico Consulting
We are an independent consulting organization providing pharmacovigilance and clinical trial services. We provide services for clinical trial, pharmaceutical, biotechnology, and medical device companies in United States, Canada, European Union.
Our diverse team of consultants work with companies to bring comprehensive solutions to complex challenges. At Clynico Consulting, our mission is to improve the health and safety of patients by delivering the highest quality of services throughout the medicinal products lifecycle.
Our diverse team of consultants work with companies to bring comprehensive solutions to complex challenges. At Clynico Consulting, our mission is to improve the health and safety of patients by delivering the highest quality of services throughout the medicinal products lifecycle.
Department
Our Medical Services
Pharmacovigilance Services
We provide comprehensive short-term and long-term Pharmacovigilance services ranging from early development support all the way through post-approval phases. We have experienced staff and skilled medical professionals to assist with:
- ICSR Management
- Risk Management Plan
- Other
- Aggregate Safety Reports
- Signal Detection
Clinical Trial Site Services
We provide comprehensive short-term and long-term Pharmacovigilance services ranging from early development support all the way through post-approval phases. We have experienced staff and skilled medical professionals to assist with:
- Source Document Review
- Site/Patient Recruitment
- Study Monitoring
- Study Initiation Documentation/Meetings
- Adverse Event Monitoring
- Regulatory Compliance
- Staff training
