FAQs

VigiSolvo is a leading Clinical Research Organization in India offering specialized services in:
Pharmacovigilance: Ensuring the safety and efficacy of pharmaceutical products.
Biobanking: Storing biological samples for research and clinical studies.
Clinical Data Management: Managing and analyzing clinical trial data for accuracy and compliance.
Pharma Manufacturing Software: Providing advanced software solutions designed to streamline pharmaceutical manufacturing processes, ensuring regulatory compliance and operational efficiency.
PV Software Solutions: Offering comprehensive software tools that support pharmacovigilance operations, including adverse event reporting, data analysis, and compliance management.
Medical Information Contact Center: Providing expert medical information services, including inquiry handling, product information management, and support for healthcare professionals and patients.

Pharmacovigilance is the science of detecting, assessing, and preventing adverse effects of pharmaceutical products. It is crucial for ensuring the ongoing safety of drugs and minimizing health risks to patients, thereby enhancing public health.

Our Clinical Data Management services involve the collection, validation, and analysis of clinical trial data to ensure compliance with regulatory standards. We provide data solutions that facilitate efficient decision-making and regulatory submissions.

Biobanking involves the collection and storage of biological samples like blood, tissue, and DNA for future research. At VigiSolvo, we follow best practices to maintain the integrity and confidentiality of the samples, ensuring their safe and efficient use in clinical studies.

VigiSolvo offers customized software solutions that streamline pharmaceutical processes, including clinical trial management, data analysis, and regulatory reporting. Our technology helps enhance operational efficiency and compliance with industry regulations.

VigiSolvo is a trusted partner with deep expertise in clinical research and regulatory compliance. We offer innovative, reliable, and compliant services tailored to your specific requirements, backed by advanced technology and a team of seasoned professionals.

Yes, VigiSolvo adheres to global regulatory standards and guidelines, ensuring that our services meet the highest levels of compliance, quality, and safety. We stay updated with industry regulations to provide solutions that align with international best practices.

Absolutely! VigiSolvo’s team of experts can assist with regulatory submissions, ensuring your clinical trials meet the required documentation, reporting, and compliance standards. We work closely with regulatory authorities to facilitate smooth approvals.

Getting started with VigiSolvo is easy! Simply contact us through our website or call our team directly to discuss your clinical research needs. We will guide you through the process and develop a customized plan that aligns with your project goals.

After your initial consultation, we will assess your specific requirements and design a tailored plan. Our team will work closely with you throughout the project to ensure timely, efficient, and successful delivery of services. Regular updates and communication ensure that you stay informed every step of the way.

You can contact VigiSolvo by filling out the contact form on our website, calling our customer service team, or emailing us directly. We’re here to answer your questions and provide you with the information you need.

Yes, VigiSolvo is committed to advancing healthcare and has been involved in multiple global research initiatives. Our expertise and cutting-edge technology make us an ideal partner for international clinical trials and studies.