Welcome to MedVigil
MedVigil Clinical Research founded in 2012 is a leading global CRO providing medical information and pharmacovigilance services to biopharmaceutical, generic pharmaceutical, consumer product, medical device, contract research and healthcare companies. We strive to promote drug safety by collecting, synthesizing and analyzing data from clinical trials and post marketed products. Our scientific expertise delivers accurate, consistent and current evidence based medical information to fulfill our client’s requests.
With a portfolio of services ranging from pre-clinical and clinical to post marketing we can promote patient safety together.
To successfully partner with healthcare organizations in order to provide high quality scientific expertise and use our knowledge to increase productivity and promote patient safety worldwide.
At Medvigil we have always believed in core values that are principles in dictating our culture and character.
Commitment to excellence
We continuously strive for excellence and quality results at MedVigil. There is no room for mediocrity.
Commitment to continuous education
Our team is constantly learning to stay abreast with the fast paced healthcare environment. We are committed to learning from experiences. Our leaders maintain an aptitude for teaching and mentoring.
Commitment to relationships
We are 100% dedicated to our clients. We value long term relationships. Our client’s growth is our growth.
Commitment to communication
We believe that effective communication leads to better outcomes and faster delivery. Our team is in constant contact with our clients no matter where they are located globally.
Commitment to teamwork
Teamwork is a crucial part of our business. Each member on our team provides individual skills to promote efficiency and quality. Each and everyone at MedVigil is responsible for the team’s growth and they work together to achieve it.
Commitment to integrity
Our employees are honest and trustworthy individuals. Everyone accepts responsibility for their work and they are authentic and straightforward while doing so.
We have the ability to focus on our client’s regulatory needs so that they can concentrate on other areas. We also have the potential to scale depending on our client’s requirements. The advantage about working with MedVigil is that clients can customize pharmacovigilance services according to their requirements. The tailor-made regulatory services portfolio will not only be cost effective but improve the quality and efficiency of your safety reporting. Our corporate headquarter is located in Mumbai, India.
MedVigil has tremendous experience in ICSR processing with over 32,000 cases completed annually. Our clients are geographically located in the US and EU.
We have worked across all therapeutic areas including but not limited to:
|Allergy and Immunology||Analgesia||Cardiology|
|Diabetes||Endocrine disorders||Gastrointestional disorders|
|Hematological disorders||Infectious disease||Neurological disorders|
|Respiratory diseases||Rheumatic disorders||Transplant|
Advantages of working with MedVigil?
- Ability to perform as needed projects for our clients such as data migration and case clean up services at short notice
- Capability of adverse event intake for reporting
- Option of all hands on board model in periods of high case volumes
- Case managers are trained on all types of cases
- A business continuity plan allows for no gaps in case processing
- Rigorous training plans of world class standard for our employees which lead to high quality output
- We will work with your operational procedures and workflows to flawlessly integrate into your environment
- Current models according to client requirements:
- To design pharmacovigilance services based on client needs
- To provide a dedicated Operations manager / Team lead to manage your project
- Continuous global communication based on project requirements
- Overtime and weekend work options for quick turn around
Our office is located in the heart of Mumbai. Our team members are highly motivated and talented individuals with unique pharmacovigilance skill sets. We have the capacity to increase and use talent within teams in our office space depending on project requirements. Our state of the art facility has the required infrastructure that allows for seamless case processing activities including two screens per person, high speed internet, backup servers and separate storage areas for each client. With our current infrastructure we have the ability to process upto 120000 cases annually.