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Unannounced Audit Case Study: A Medical Device Manufacturers Experiences

by Q1Web Admin | Sep 8, 2018 | Archived Webinar, Content Library

Unannounced Audit Case Study: A Medical Device Manufacturers Experiences ; Access Webinar Here Related Event Here Join Mailing List In an effort to strengthen medical device safety and efficacy, the EU Commission implemented the Recommendation of 2013/473/EU, a policy...

Tools and Techniques to Ensure Successful Outcomes in Device GCP Audits

by Q1Web Admin | Sep 8, 2018 | Archived Webinar, Content Library

Tools and Techniques to Ensure Successful Outcomes in Device GCP Audits ; Access Webinar Here Related Event Here Join Mailing List The FDA has implemented stricter regulatory requirements for medical device clinical studies and are now requiring vast amounts of...

Implementing New Responsibilities for Economic Operators under the EU MDR

by Q1Web Admin | Sep 8, 2018 | Archived Webinar, Content Library

Implementing New Responsibilities for Economic Operators under the EU MDR ; Access Webinar Here Related Event Here Join Mailing List The MDR, published in in May 2017, has updated and clarified a variety of roles and responsibilities within the medical device supply...

CMC Case Study: Best Practices in FDA Meeting Preparation Strategies

by Q1Web Admin | Sep 7, 2018 | Archived Webinar, Content Library, Life Science Webinar

CMC Case Study: Best Practices in FDA Meeting Preparation Strategies ; Access Webinar Here Related Event Here Join Mailing List Throughout the drug development and product approval process, CMC executives have a limited number of opportunities to engage with FDA to...

Reviewing OPDP Enforcement Actions and Best Practices for Compliant Drug Promotion

by Q1Web Admin | Sep 6, 2018 | Archived Webinar, Content Library

Reviewing OPDP Enforcement Actions and Best Practices for Compliant Drug Promotion ; Access Webinar Here Related Event Here Join Mailing List The number of warning and untitled letters from the FDA’s Office of Prescription Drug Promotion (OPDP) has been on the decline...

FDA Regulatory Due Diligence in Mergers and Acquisitions for Medical Device Companies

by Q1Web Admin | Sep 6, 2018 | Archived Webinar, Content Library

FDA Regulatory Due Diligence in Mergers and Acquisitions for Medical Device Companies ; Access Webinar Here Related Events Join Mailing List Whether your company is acquiring other device companies, or itself may be acquired, it is critical to understand the process...
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Since TrainingPros was founded in 1997, we have been dedicated to helping our clients find the right consultant for their projects. 25 years later, we are proud to have helped hundreds of clients complete their projects and thousands of consultants find great assignments. We continue to focus on helping our clients and consultants as well as our community as a certified women-owned, award-winning staffing company that works exclusively with Learning & Development professionals to match consultants to client projects.

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TELCOR is the proven leader of health care software solutions for revenue cycle management (RCM) software and services designed specifically for laboratories. TELCOR RCM, our SaaS solution, and TELCOR Revenue Cycle Services, our billing service, are designed to streamline workflow, improve collections, and provide real-time analytics. Our software and service solutions are designed for the unique challenges and requirements of laboratory specialties and the clients they serve. With full access to data, labs have complete visibility of their data and can track key performance indicators. No other vendor works as hard ensuring you get paid for the work you do.

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Policy Reporter, acquired by TrialCard in 2019, provides innovative healthcare software solutions to track payer policies in near real-time and enhances market access for the therapies patients need most. The company’s patented software-driven solutions include a suite of billing and reimbursement tools for providers and laboratories, market intelligence tools for payers, and a suite of market access solutions for life science companies. Its clients include some of the world’s largest pharmaceutical and healthcare companies. 

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TELCOR is the proven leader of health care software solutions for revenue cycle management (RCM) software and services designed specifically for laboratories. TELCOR RCM, our SaaS solution, and TELCOR Revenue Cycle Services, our billing service, are designed to streamline workflow, improve collections, and provide real-time analytics. Our software and service solutions are designed for the unique challenges and requirements of laboratory specialties and the clients they serve. With full access to data, labs have complete visibility of their data and can track key performance indicators. No other vendor works as hard ensuring you get paid for the work you do.

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