PV Services
Welcome to our dedicated Pharmacovigilance Consulting Services page. Our mission is to ensure the highest standards of safety and efficacy for pharmaceutical products, protecting both patients and manufacturers. With a team of experienced pharmacovigilance professionals, we offer a comprehensive suite of services designed to navigate the complex landscape of drug safety.
Our Services Include:
- Risk Management and Mitigation Strategies
- Regulatory Compliance
- Signal Detection and Management
- Adverse Event and Case Report Processing
- Pharmacovigilance Audits and Inspections
- Pharmacovigilance Training
- Literature Review and Surveillance
- Benefit-Risk Assessment
Pharmacovigilance Training
Providing tailored training programs for your team to enhance their understanding of pharmacovigilance principles, processes, and regulatory requirements, ensuring best practices are followed.
Local QPPV Service
Developing and implementing risk management plans to identify, evaluate, and minimize the risks associated with pharmaceutical products, ensuring patient safety and compliance with regulatory requirements.
Audit/ Inspection
Conducting audits and preparing for regulatory inspections to ensure pharmacovigilance systems are compliant with global standards and regulations. Our proactive approach helps identify and rectify potential issues before they become compliance risks.
Literature Screening
Continuous monitoring of scientific literature and databases for information relevant to the safety of your products. This includes literature searches, reviews, and reporting of relevant findings to regulatory authorities.
ICSR Management
Offering timely and accurate processing of adverse event reports, from intake through to submission to regulatory authorities. Our meticulous approach ensures compliance and enhances drug safety profiles.
Regulatory Intelligence
Assisting with the preparation of necessary documentation and reports to meet the regulatory requirements of various health authorities, including the CDSCO, Indian Pharmacopoeia Commission, and others. Our services ensure that your products comply with all pharmacovigilance obligations.
Why Choose Us?
- Expertise: Our team comprises seasoned pharmacovigilance experts with extensive experience in the pharmaceutical industry and regulatory affairs.
- Tailored Solutions: We offer customized services to meet the unique needs of each client, ensuring optimal outcomes.
- Global Compliance: With deep knowledge of international regulations and guidelines, we ensure your products meet global safety standards.
- Commitment to Safety: At the core of our services is a relentless commitment to patient safety and product efficacy.
Reviews
Tom S.
“The pharmacovigilance training programs offered by CMPV Consultancy are simply outstanding. Tailored to our company’s specific needs, the training was engaging, informative, and highly practical. It has significantly enhanced our team’s capabilities and understanding of drug safety. We’ve seen a noticeable improvement in our pharmacovigilance practices thanks to their expert training.”
Liz S.
“My experience with CMPV Consultancy was exceptional. Their team of pharmacovigilance experts is not only deeply knowledgeable about the latest regulations but also incredibly proactive in managing our company’s drug safety processes. Their attention to detail and commitment to ensuring compliance has been instrumental in our project’s success. Highly recommend their services to anyone in need of top-notch pharmacovigilance consulting.”
Mike A.
“CMPV Consultancy’s expertise in risk management has been a critical asset to our organization. Their strategic approach to identifying, assessing, and mitigating risks has not only improved our product safety profile but also streamlined our reporting processes. Their insights and recommendations have been invaluable. A trusted partner in pharmacovigilance!”
ClovisMed pharmacovigilance Consultancy 