Regulatory Intelligence
The ever-evolving Pharma, Biotech, and Drug Device industries are governed by regulations, these regulations are constantly changing to help the pharma companies provide their best services to the consumers. Keeping up with the regulations on a regular basis can be a major challenge for companies across the life sciences industry. You need a pharmacovigilance partner that does the work on your behalf and keeps you updated on the latest regulations so that you can comply with the regulations and deliver your best. We understand the impact of regulations and their needs for your organization, vizen life science’s robust regulatory intelligence services will help you in managing the recent global regulatory developments without manually tracking the hundreds of regulatory information sources.
Our Services
Vizen life sciences provide you with robust PV regulation intelligence services. Our services include gathering, interpreting, and summarizing the regulation information related to Pharmacovigilance. We regularly monitor the information from global, local, and regional authorities relating to pharmacovigilance. We make sure that our clients are up to speed about all the news related to the latest regulatory information and requirements. Vizen life sciences offer our clients advice on the regulations and guidelines related to pharmacovigilance in individual countries. We also maintain regional, country specific case reporting and aggregate reporting requirements. We conduct regular research to cover the data related to country-specific updates, congress, regulatory updates, trade associations, key leaders and influencers’ opinions, authority & ministry. As a part of our regulatory intelligence services, we also regularly monitor newsletters, websites, and RSS feeds of the international standards organization and regulation authorities, blogs, and relevant articles.
- Region and product-specific guidance
- Country-specific regulatory updates, aggregate reporting & ICSR requirements, and timelines
Why Vizen Life Sciences?
Vizen Life Sciences has highly trained professional staff that provides a variety of pharmacovigilance services to our clients. Vizen delivers flexible services that match the specific requirements of our clients. Our team’s unparalleled expertise has helped us in delivering premium-quality regulatory intelligence services. We are committed to delivering quality-driven, transparent, and, flexible pharmacovigilance services to our clients. We provide our clients with services that help them in creating internal regulatory and PV processes that comply with the policies and laws. Our cost-effective solutions & processes make pharmacovigilance more efficient and straightforward. We follow rigorous quality control processes to stay in accordance with regulatory standards. We identify and monitor the potential and identify risks to ensure patient safety.
Global Services
- Safety Database
- Adverse Events (AEs) Reporting
- Aggregate Reporting
- Pharmacovigilance Literature Search
- Pre-Preparation and Submission of Aggregate Reports
- Safety Signal Detection Services
- Risk Management Services
- Regulatory Intelligence
- Ongoing Monitoring Services
- Medical Devise Vigilance Services
- Pharmacovigilance Consultancy Services
Contacts
Visit Us
10th Floor Kapil Towers, Survey 115/1, ISB Rd, Financial District, Gachibowli, Nanakaramguda, Telangana 500032
Have Any Questions?
040-69441100
Mail Us
info@vizenlifesciences.com