QPharma enables pharmaceutical and biotechnology companies to launch and commercialize new products with rigorous adherence to state, federal, and international regulations. Founded in 1994 and with offices globally, QPharma employs qualified compliance and brand consultants.
Contact us today today to learn more about our Titanium® platform and put our expertise to work.
QPharma’s Titanium® platform offers a comprehensive solution encompassing all your sample management needs. QPharma’s Ti Sample® solution sample management and distribution services including:
- Sample Accountability
- Field Inventory Services
- Practitioner Validation
- Licensing Solutions
- Sample Storage and Fulfillment
Ti Order Point®
- Branded, web ordering portal for sales representatives to place orders for samples and marketing materials
- Manage requests for bulk shipments
- Place push shipments to multiple sales teams at the click of a button
- Complete orders for conventions
QPharma enables our clients to deliver samples and literature quickly into the hands of healthcare professionals — with or without the involvement of a sales representative, and thanks to QPharma’s purpose-built HCP self-service solution, Ti Portal®, which features:
- HCP Sample Ordering and Easy Reordering
- Convenient Electronic Acknowledgement of Content (AOC) Sign-off
- Integrated Practitioner Validation
- Direct-to-Patient Sample Ordering
- Direct-to-Practitioner Fulfillment
- Contact Center Services for HCP Follow-Up and Inquiries
QPharma offers a comprehensive range of live and on-demand training services across the entire life science enterprise. Whether selecting from our extensive library of courses or working with QPharma’s instructional designers and subject matter experts to develop new training modules, QPharma’s clients can have peace of mind that their entire organization from field sales to human resources, clinical and manufacturing will have easy access to the top-quality training they need. Training services and solutions include:
- Ti LMS®, Learning Management System
- Live Classroom-based Training
- Compliance Course Library
- SCORM-compliant LMS Course Design
- Integration with Titanium®
Compliance with federal and state transparency regulations is vital for commercial success. Solutions offered by QPharma include:
- Federal Reporting under the Patient Protection and Affordable Care Act (ACA)
- State Spend Transparency Reporting
- State Sample Transparency Reporting
- Transparency Compliance Services
For life science companies preparing for a product launch, it is vital that every step of the process — from clinical trials to pre-commercialization and regulatory preparation, to launch and beyond — be carefully tracked and managed. With QPharma’s purpose-built technology platform, Ti Launch®, and access to our expert team of consultants, clients and brands of every size will be positioned for a successful global launch. QPharma’s product launch management solution includes:
- Launch Planning
- Rapid Launch Methodology
- Consultative Support
QPharma opened its doors as a Professional Services company in 1994. Today, consultative professional services for life sciences remains the foundation upon which our compliance-focused reputation is based. Our experienced team of consultants work directly with our pharmaceutical, biotechnology, and other life sciences clients to achieve each of their compliance goals.
- Management Consulting
- Program and Project Management
- Compliance Services
- Validation Services
QPharma is a leading provider of KOL/expert identification, mapping, and management services, all housed within the purpose-built Titanium® platform. Our expert mapping solutions include:
- Gap and Landscape Analysis
- KOL Influence Mapping and Engagement Planning
- KOL Compliance Validation
- Sunshine Act Analysis
Make your sales teams more effective in the field with Ti CRM® ,the first-ever salesforce automation system purpose-built for the Titanium® platform.
Ti CRM® features and benefits include:
- Intuitive User Interface
- Pre-populated Samples Request Form Generation
- Integrated Hand-Carry and DTP Request Capture
- Acknowledgement of Content (AOC) Follow-Up Capability
- Pharmacy Sample Drops with Dual-Signature Capture
- Video Conferencing Capable
- Built-in Practitioner Validation
- Prescription Drug Marketing Act (21 CFR Part 203)PDMA, 21 CFR Part 11, and State Regulations Compliant