QPharma: Next Gen Compliance Tools
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QPharma: Next Gen Compliance Tools

The pharmaceutical industry is falling under increased scrutiny across the value chain from drug discovery to post-marketing surveillance. Pharma organizations are understandably focused to take care of the patient safety issues where failures can jeopardize the future of the entire landscape. Alongside, changes in regulation are forcing pharmaceutical companies to renew their focus on compliance. The Morristown, NJ based QPharma provides regulatory compliance and brand support solutions to pharmaceutical, medical device, biotechnology, and other allied life sciences industries. The company is committed to quality in every aspect of its services, operations and customer relations. It provides compliance consulting and program development designed to mitigate risk and diversion of controlled substances in accordance with Drug Enforcement Administration (DEA) and State Board of Pharmacy regulations.

QPharma’s Titanium—an integrated suite of SaaS-based compliance, analytics, and training tools provides sales representatives, home office users, and other life sciences personnel with dashboard-level access to information about their compliance and commercial operations. Formerly known as Python, QPharma has rebranded its flagship technology platform as Titanium. Titanium includes a variety of integrated modules associated with consultation and assessment services to give effective insights into the client’s business intelligence.

QPharma through its QPid solution enhances practitioner validation service. From State License Number, to National Provider Identifier, to Drug Enforcement Agency data, QPid is an end-to-end solution for pharmaceutical, medical device, and biotech firms seeking to verify healthcare provider eligibility for product sampling and Sunshine Act compliance. As a service provider, The company dedicates all resources, knowledge, time, and experience in completing projects in an efficient, cost-effective, and timely manner. To introduce life sciences companies to the solution, QPharma is offering to auto-match 5,000 practitioner records on trial basis, for a limited time. “In contrast to many firms offering license validation services, we offer a full continuum of sample accountability and fulfillment solutions under one roof,” asserts Patrick Den Boer, President and CEO of QPharma.

QPharma is committed to quality in every aspect of services, operations and customer relations


Being a premier provider of compliance and commercial services to the life sciences industry, QPharma offers qSpend—an aggregate spend compliance and reporting solution that enables to track and report on professional fees, gifts, promotional activities, and other payments to healthcare practitioners. The web-based solution, qSpend is fully configurable and includes customer-specific administrative preferences, thresholds, and alerts to provide on-demand access anytime, anywhere.

QPharma’s solutions are built on a robust foundation of quality and regulatory compliance, enabling clients to continue their acceleration by following complex guidelines and regulations enforced by FDA, CMS, and other regulatory authorities. As medical device manufactures are constrained to comply with industry-altering regulations, QPharma’s seasoned medical device subject matter experts carefully monitor the evolving requirements for Unique Device Identification (UDI) compliance. The firm helps companies achieve total compliance by identifying their appropriate product labeling standards and ensuring that the clients have applied the right UDI-compliant label, to the right product, at the right time while manufacturing the device.

Having been in the marketplace for more than two decades, the firm expertly addresses the needs surrounding highly regulated environments, bringing to the forefront a clear understanding that allows clients to move confidently and without risk towards production and compliance goals. Good compliance equals to good business. In the near future, QPharma aims to be the cynosure of pharmaceutical compliance solutions by rolling out improved features and functionality for Titanium.