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Your Vision. Our Solutions.

At Curix, we believe in providing customized solutions to Life Science companies to support and enhance your organization’s success. With our fit for purpose model, we offer services to meet the data entry, processing and management needs for a wide range of activities in the life sciences space, including pharmacovigilance and safety, patient support services and market research.  Our data center services are complimented by our medical writing suite for clinical documents and scientific communications.  Our service model is fully customizable to fit your unique needs and we are able to tailor our solutions to meet your requirements.  We’re committed to excelling at our job, so you can focus on yours.

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Your Reliable Services Partner

Curix was established by executives from the Pharmaceutical and Information Technology industries, to provides services to Life Sciences companies to support their needs for contact and data center, pharmacovigilance and medical writing.  Having extensive experience in these fields, we are uniquely positioned to understand the needs of our Life Science clients and translate them into customized and workable solutions, without interrupting your workflows.  We have deep subject matter expertise in pharmaceutical data collection and management, drug development, pharmacovigilance and safety services, patient support services, compliance and ethics.  Our HIPAA compliant services can be customized to your requirements in order to offer a seamless experience.

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Our strategy is flexible to your needs and, being a nimble organization with a deep commitment to quality, we are able to tailor our services and delivery to your standards, safeguarding your company’s values. 

It is our policy to provide services which conform to global regulations and guidelines and meet the requirements of our clients, with quality and on time. We are fully committed to achieving a high standard of personal and corporate excellence.


We create “fit for purpose” resourcing and functional solutions for our clients by listening to your needs. Our commitment to your success is evident in the flexible and scalable model that we operate under. We leverage our resources to extend and enhance your capabilities, whether it be to set up a new process, outsource an existing activity or to manage work overflow and demand. 

Our Data and Contact Center caters specifically to the needs of Life Science companies.  We provide data entry, processing and management services for a wide range of activities including, but not limited to, adverse events, serious adverse events, product complaints, medical device complaints, patient support intake forms, patient testimonials and market research surveys.  This comprehensive service is designed to fit your unique needs without disrupting productivity or workflow.

We have stringent quality control measures in place, including checks for language, data accuracy and adherence to client requirements.  All Protected Health Information (PHI) processed through our contact and data center is handled in a manner compliant with the Health Insurance Portability and Accountability Act (HIPAA) and General Data Protection Regulation (GDPR).  We are also positioned to meet any other regulatory needs specific to activities defined by the client and applicable industry guidelines such as ICH GCP guidelines.


Our Drug Safety physicians and subject matter experts provide unparalleled expertise to our clients and aim to be a trusted partner to your team in supporting their pharmacovigilance needs and advising on strategies to implement and improve processes related to patient safety.  Some of the services included in our Pharmacovigilance suite, for both pre- and post-marketing products, include:

  • Create standard operating procedures (SOPs) that are specific to the needs of the client

  • Case processing and data entry for adverse event, serious adverse event (SAEs), product and device complaints

  • Medical review of SAEs and writing patient narratives

  • Signal detection

  • Creating periodic aggregate reports and risk management plans

  • Pharmacovigilance and safety reporting training for the organization and employees


We provide medical writing services for drafting of clinical documents as well as scientific communications and education materials. 

Our clinical writing offerings include study protocols, protocol amendments, Clinical Study Report (CSR), Investigator Brochure (IB), Informed Consent Form (ICF), patient information materials, patient safety/case narratives, safety reports and SOPs covering drug development activities (design, conduct and reporting of clinical trials, including SOPs required for oversight by Sponsors for outsourced clinical trials) and pharmacovigilance.  We also support publishing of documents for regulatory submissions. 

Our scientific communication services include manuscript writing, abstracts, posters, slide presentations, editorial support, publication planning and literature reviews.

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Services you can depend on

Members of our senior leadership are based out of the Boston area, providing convenient access during US business hours


Deep domain expertise

Curix was founded by executives from the Pharmaceutical and Information Technology industries. We have a deep understanding of the Pharmaceutical industry and associated regulations, data processing and management, pharmacovigilance and drug development.


Fit for Purpose model

We create “fit for purpose” resourcing and functional solutions for our clients, which can be scaled to suit client needs.

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Our Quality Commitment 

Our aim is to provide services with quality through our solutions designed specifically for your process.  Curix's comprehensive Standard Operating Procedures are backed by customized Operating Guidelines specific to each client’s activities, with instructions for every step of the workflow.  Quality and compliance to Standard Operating Procedures and Operating Guidelines are assessed by Curix on a continual basis. Employee abilities are assessed through internal certification programs and extensive training and guidance is provided to ensure that quality and consistency are maintained.

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Contact us today to learn more about our business and how we can help you.


159 Indian Pipe Lane Concord MA 01742


4510, Sector 23A, Gurgaon Haryana 122017

781 552 6523

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