Innovative Training for Medical Device Core Good Manufacturing Practice Provided by Regulatory Compliance Associates Inc. and Invenio University

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The Medical Device Core Good Manufacturing Practice (MDCGMP) program is a world-class, concentrated, interactive training experience offered November 14 through December 9, 2011 in Guanacaste, Costa Rica. The unique program focuses on providing a holistic look at Good Manufacturing Practices (GMPs) as they relate to the medical device industry. Participants will gain a core level understanding of GMPs, FDA expectation and industry practice.

“The program is unique because students will review case studies and experience real-life situations, along with other interactive activities as a means to increase knowledge retention” according to Steve Schultz, Executive Vice President of RCA.

The Medical Device Core Good Manufacturing Practice (MDCGMP) program is a world-class, concentrated, interactive training experience offered November 14 through December 9, 2011 in Guanacaste, Costa Rica. The unique program focuses on providing a holistic look at Good Manufacturing Practices (GMPs) as they relate to the medical device industry. Participants will gain a core level understanding of GMPs, FDA expectation and industry practice.

The MDCGMP program is offered by life science experts, Regulatory Compliance Associates Inc., and Invenio University. “This unique training program is driven by our vision to make Costa Rica the leading medical device manufacturer in the world,” says Adrian Lachner, of Invenio University.

The MDCGMP program is delivered by subject matter experts, representing many years of experience in the regulated quality world or medical devices, and include guest speakers from the FDA and local companies. Participants will work through 24 learning modules, starting with basic subjects such as GMP Fundamentals and Good Documentation Practices (GDPs), finishing with more advanced modules such as Contributing to a Successful Quality Culture and Adverse Findings/Consequences.

Modules are designed to demonstrate the true interrelationship of all the GMP elements, reflective of how they are actually related in industry. “The program is unique because students will review case studies and experience real-life situations, along with other interactive activities as a means to increase knowledge retention” according to Steve Schultz, Executive Vice President of Regulatory Compliance Associates.

Registration, including scholarships, is available on a first-come, first-serve basis. Class size is limited to ensure participants receive appropriate attention. Contact Steve Schultz at S.Schultz(at)rcainc(dot)com or dial (262) 842-1250 for more information.

About Regulatory Compliance Associates Inc.

Regulatory Compliance Associates (RCA) is a global consulting firm providing technically-driven, regulatory and quality solutions to cGMP and operational related challenges for the Life Sciences industries. RCA brings full‐spectrum solutions including top-tier strategic planning, mid-level project management, and hands-on analyst support to provide a customized plan to meet clients’ needs, on time and on budget.
http://www.rcainc.com

About Invenio University

Invenio University, located in Guanacaste, Costa Rica, is committing to making Costa Rica the leading country for medical device manufacturing. To accomplish this mission, Invenio created the Medical Device Training Center (MDTC). The MDTC builds a constant flow of highly trained talent through specialized training and shared services that help our customers meet the human capital challenges of the medical device industry.
http://www.mdtrainingcenter.com

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